Few stocks have delivered as compelling a performance over the past year or so as Sandisk (SNDK 0.04%). The memory specialist has delivered monster returns for investors who picked up shares shortly after its spinoff from Western Digital, which bought it in 2016.
If you had the foresight to invest $30,000 during the spinoff (which occurred on Feb. 24, 2025) and held on through the astonishing run that followed, the value of your stake would now be more than $1 million. That's an incredible gain in just over a year's time.
But for those investors who haven't already gotten into the stock, the question is, can Sandisk's run continue, or has it reached its peak?
Image source: Getty Images.
Sandisk is thriving thanks to rising memory chip prices Sandisk makes NAND memory, which is primarily utilized for long-term data storage. Its products are mostly used to make solid-state drives (SSDs), which are used in data centers to house data and information. Sandisk and its peers don't have the production capacity to make enough NAND for SSDs to meet soaring data center demand. As a result, prices for these commodity components have soared, and Sandisk's revenues and profits have skyrocketed.
Sandisk is currently in the fourth quarter of its fiscal 2026. For this period, Wall Street analysts expect 332% year-over-year revenue growth. For fiscal 2027, Wall Street analysts expect 118% growth. That demonstrates how much the prices of memory are soaring, and the shortage driving those price hikes could last for a long time as data center spending continues to ramp up.
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A great source of insight about the future pace of data center expansion is Nvidia (NVDA 3.39%). The world's largest company has its fingers on the AI build-out pulse, and is a close partner with every AI company. Those relationships are helping it plan to meet demand for its AI accelerators down the road. While the big four AI hyperscalers say they plan to lay out about $650 billion in data center capital expenditures during 2026, Nvidia told investors that their collective capex will top $1 trillion in 2027. Furthermore, by 2030, it expects global annual data center capital expenditures to reach $3 trillion to $4 trillion.
Those new data centers will need more than just an enormous quantity of AI accelerators -- they'll also need a ton of memory, which bodes well for the long-term outlook of Sandisk. In that context, investors shouldn't view it as some flash-in-the-pan company that rises massively one year, then plunges the next. Its business will have a ton of staying power as long as the AI data center build-out is ongoing and as long as the production capacity of memory-chip makers lags behind demand. Once the AI build-out slows, Sandisk's stock may fare poorly, but it could be many years before that happens. As a result, Sandisk's stock could still be a smart AI investment.
Keithen Drury has positions in Nvidia. The Motley Fool has positions in and recommends Nvidia and Western Digital. The Motley Fool has a disclosure policy.
The memory market is booming, with TrendForce recently raising its global memory forecasts for both 2026 and 2027. It now sees the market hitting $889.3 billion in 2026, with $618.7 billion coming from DRAM (dynamic random-access memory) and $270.6 billion from NAND (flash). That's up from a prior outlook of $551.6 billion. For 2027, it raised its forecast from $842.7 billion to $1.28 trillion.
Both the DRAM and NAND markets have been seeing prices surge due to a demand-supply imbalance, stemming from the artificial intelligence (AI) infrastructure build-out. Graphics processing units (GPUs) and other AI chips need to be packaged with high-bandwidth memory (HBM), a specialized form of DRAM, to optimize performance, and the shift toward inference and agentic AI is increasing demand. In turn, with DRAM manufacturers focused on producing high-margin HBM, prices for ordinary DRAM have also gone through the roof.
NAND prices have also been flying higher. The industry cut back production after flash prices crashed following the pandemic, and it has been slow to come back online, with the big memory makers largely focused on DRAM and HBM. At the same time, demand for huge solid-state drives (SSDs) that use flash has been soaring due to AI.
Let's look at three ways investors can play the torrid memory market with two semiconductor stocks and one exchange-traded fund (ETF).
Image source: Getty Images
1. Micron Micron (MU 3.81%) is one of the world's big three DRAM makers, and the only one based in the U.S. About 80% of its revenue comes from DRAM, with the rest largely from NAND.
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The company has been riding the memory wave, with surging revenue and ballooning gross margins. Last quarter, saw its revenue nearly triple to $23.9 billion, while its gross margins climbed from 36.8% a year ago to 74.4%. That led to its adjusted EPS skyrocketing from $1.56 a year ago to $12.20 in its fiscal Q2.
With demand soaring, Micron has started to move toward signing long-term multiyear deals for the first time. This should help reduce some of the cyclicality of its business and provide it with better visibility. Meanwhile, the stock is not pricey, trading at a forward P/E of just 9 times fiscal 2027 analyst estimates.
2. Sandisk Sandisk (SNDK 0.04%) is a pure play on NAND flash. Similar to the dynamics with DRAM, it is also seeing surging prices driving revenue higher and expanding gross margins.
For its fiscal Q3, the company's revenue soared 251% year over year to $6 billion, as data center revenue rocketed 645% to $1.4 billion. Gross margin, meanwhile, climbed from 22.5% a year ago to 78.4%. This led to its adjusted EPS going from a loss of $0.30 to a profit of $23.41.
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Similar to Micron, Sandisk also started signing long-term deals. It currently has five deals in place covering a third of its capacity in fiscal 2027, with the longest deal extending five years. The deals include both fixed and variable pricing and have protections in place. The company is also starting to develop high-bandwidth flash (HBF), which could be a big growth driver in the coming years.
Sandisk stock is also not expensive, trading at a forward P/E of just 9 times the fiscal 2027 analyst consensus (ending June 2027).
3. DRAM - Roundhill Memory ETF Another great way to play the memory market is with the DRAM - Roundhill Memory ETF (DRAM 4.16%). The nice thing about the exchange-traded fund is that it gives investors exposure to the big international memory companies. While Micron is one of the big three memory makers, Korean companies SK Hynix and Samsung are generally viewed as the market leaders.
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Currently, Micron makes up 30% of the ETFs' holdings, followed by SK Hynix at 24.5%, and Samsung at 18.4%. SK Hynix currently doesn't have American Depository Receipts and thus doesn't trade in the U.S. However, it is perhaps the best-positioned of the companies, having a close relationship with Nvidia and recently entering a multiyear partnership with the chip giant to co‑develop next‑generation memory. It also reportedly supplies more than 60% of Nvidia's HBM4 volumes for its Vera Rubin platform. The DRAM ETF is one of the best ways to invest in the company.
Ucore Rare Metals Inc. (OTCMKTS:UURAF - Get Free Report)'s stock price passed above its 200-day moving average during trading on Thursday. The stock has a 200-day moving average of $4.79 and traded as high as $5.05. Ucore Rare Metals shares last traded at $4.8780, with a volume of 103,633 shares changing hands. Analyst Upgrades
Ucore and Vulcan Elements executed a Memorandum of Understanding to build a domestic, secure rare earth magnet supply chain for defense and commercial applications.Ucore will provide initial NdPr and Dy oxide samples to Vulcan this year, leading to a long-term commercial supply agreement beginning in 2027.Together, Ucore and Vulcan Elements are onshoring an integrated rare earth magnet supply chain. Ucore's Louisiana Strategic Metals Complex will directly feed Vulcan's North Carolina manufacturing facilities.Vulcan announced a $1.4 billion partnership with the United States Government to build the largest rare earth magnet factory in the world outside of China, with 10,000 metric tonnes of magnet manufacturing capacity.Halifax, Nova Scotia--(Newsfile Corp. - March 24, 2026) - Ucore Rare Metals Inc. (TSXV: UCU) (OTCQX: UURAF) ("Ucore" or the "Company") is pleased to announce the execution of a Memorandum of Understanding dated March 16, 2026 with Vulcan Elements Inc. ("Vulcan") to collaborate on the development of a domestic rare earth magnet supply chain for defense and commercial applications. Under the agreement, the parties intend to finalize a full commercial supply partnership whereby Ucore would supply Vulcan with NdPr oxide and Dy oxides at commercial scale beginning in 2027.
The collaboration aligns Ucore's demonstrated separation platform at its Commercial Demonstration Facility ("CDF") in Kingston, Ontario, and its planned Louisiana Strategic Metals Complex ("SMC") in Alexandria, Louisiana, with a leading American magnet manufacturer. Vulcan currently operates a commercial magnet manufacturing facility in Durham, North Carolina, and is expanding to a 10,000 tonne magnet manufacturing facility in Benson, North Carolina. The facility is enabled by a $1.4 billion partnership with the United States Government, including the Department of War and the Department of Commerce. In May 2025, Ucore announced an $18.4 million Award by the Department of War to develop its rare earth processing capabilities in Louisiana.
Ucore intends to make a portion of its planned Louisiana SMC capacity available to Vulcan beginning in 2027. The collaboration would create a direct commercial bridge from Ucore's demonstration-scale separation work in Kingston to commercial-scale production in Louisiana, while supporting Vulcan's manufacturing in North Carolina.
Pat Ryan, P.Eng., Chairman & Chief Executive Officer of Ucore, stated:
"Vulcan is building exactly the kind of downstream magnet platform that the United States needs, and this partnership creates a winning commercial partnership that aligns Ucore's separation capability with an industry-leading U.S. manufacturer. Our collaboration will anchor a resilient allied rare earth magnet supply chain in the United States."
John Maslin, Chief Executive Officer of Vulcan Elements, commented:
"Since its inception, Vulcan Elements' mission has been to build a domestic rare earth magnet supply chain that can propel America into the 21st century and enable the next era of innovation and national security. Vulcan's partnership with Ucore is a milestone for both companies, and for the United States of America. Together, we're rebuilding a core industry that is critical for economic growth and national security."
This year, Ucore and Vulcan intend to advance initial production, testing protocols, purity targets, acceptance criteria, and other technical specifications in support of Vulcan's magnet manufacturing capability-leading to a longer-term commercial supply agreement.
#
About Ucore Rare Metals Inc.
Ucore is focused on rare- and critical-metal resources, extraction, beneficiation, and separation technologies with the potential for production, growth, and scalability. Ucore's vision and plan is to become a leading advanced technology company, providing best-in-class metal separation products and services to the mining and mineral extraction industry.
Through strategic partnerships, this plan includes disrupting the People's Republic of China's control of the North American REE supply chain through the near-term development of a heavy and light rare-earth processing facility in the US State of Louisiana, subsequent SMCs in Canada and Alaska and the longer-term development of Ucore's 100% controlled Bokan-Dotson Ridge Rare Heavy REE Project on Prince of Wales Island in Southeast Alaska, USA ("Bokan").
Ucore is listed on the TSXV under the trading symbol "UCU" and in the United States on the OTC Markets' OTCQX® Best Market under the ticker symbol "UURAF."
For further information, please visit www.ucore.com.
About Vulcan Elements
Vulcan Elements manufactures sintered permanent neodymium iron boron (NdFeB) magnets in the United States for critical defense and commercial applications. NdFeB magnets convert electricity into motion. They are essential components in almost every advanced machine and electronic device-from AI data centers and semiconductor fabrication equipment to satellites, drones, robotics, electric motors, and virtually all military platforms. Vulcan remains committed to advancing technological innovations, galvanizing America's manufacturing workforce, and collaborating with both public and private sector stakeholders to strengthen the domestic rare earth magnet supply chain.
For further information, please visit www.vulcanelements.com
Forward-Looking Statements
This press release includes certain statements that may be deemed "forward-looking statements". All statements in this release (other than statements of historical facts) that address future business development, technological development and/or acquisition activities (including any related required financings), timelines, events, or developments that the Company is pursuing are forward-looking statements. Although the Company believes the expectations expressed in such forward-looking statements are based on reasonable assumptions, such statements are not guarantees of future performance or results, and actual results or developments may differ materially from those in forward-looking statements.
Regarding the disclosure in the press release above about government support for Ucore, the Company has assumed that the applicable projects (including each of the associated milestones) will be completed satisfactorily and in accordance with the respective agreements or letters of intent (as applicable) for such government support. For additional risks and uncertainties regarding the Company, its business activities, its ability to qualify for and receive any additional funding from any U.S. or Canadian government, the CDF and the aforementioned projects (generally), see the risk disclosure in the Company's MD&A for Q4-2025 (filed on SEDAR+ on May 18, 2025) (www.sedarplus.ca) as well as the risks described below.
Regarding the disclosure above in the "About Ucore Rare Metals Inc." section, the Company has assumed that it will be able to procure or retain additional partners and/or suppliers, in addition to Innovation Metals Corp. ("IMC"), as suppliers for Ucore's expected future SMCs. Ucore has also assumed that sufficient external funding will be found to continue and complete the ongoing research and development work required at the CDF and also later prepare a new National Instrument 43-101 technical report that demonstrates that Bokan is feasible and economically viable for the production of both REE and co-product metals and the then prevailing market prices based upon assumed customer offtake agreements. Ucore has also assumed that sufficient external funding will be secured to continue the development of the specific engineering plans for the SMCs and their construction and eventual commissioning and operations. Factors that could cause actual results to differ materially from those in forward-looking statements include, without limitation: IMC failing to protect its intellectual property rights in RapidSX™; RapidSX™ failing to demonstrate commercial viability in large commercial-scale applications; Ucore not being able to procure additional key partners or suppliers for the SMCs; Ucore not being able to raise sufficient funds to fund the specific design and construction of the SMCs and/or the continued development of RapidSX™; adverse capital-market conditions; unexpected due-diligence findings; the emergence of alternative superior metallurgy and metal-separation technologies; the inability of Ucore and/or IMC to retain its key staff members; a change in the legislation in Louisiana or Alaska and/or in the support expressed by the Alaska Industrial Development and Export Authority (AIDEA) regarding the development of Bokan; the availability and procurement of any required interim and/or long-term financing that may be required; and general economic, market or business conditions.
Neither the TSXV nor its Regulation Services Provider (as that term is defined by the TSXV) accept responsibility for the adequacy or accuracy of this release.
To view the source version of this press release, please visit https://www.newsfilecorp.com/release/289691
Source: Ucore Rare Metals Inc.
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Halifax, Nova Scotia--(Newsfile Corp. - March 31, 2026) - Ucore Rare Metals Inc. (TSXV: UCU) (OTCQX: UURAF) ("Ucore" or the "Company") is pleased to acknowledge the recent announcement by it's partner, Hastings Technology Metals Limited ("Hastings"), in partnership with Wyloo , regarding the acquisition of a fully-permitted hydrometallurgical mixed rare earth chloride ("MREC") production facility in Thailand. Ucore congratulates Hastings and Wyloo ("the Yangibana Joint Venture Partners") on this strategic acquisition, which is expected to accelerate their ability to process third-party monazite feedstock prior to development of the Yangibana Project.
Halifax, Nova Scotia--(Newsfile Corp. - April 7, 2026) - Ucore Rare Metals Inc. (TSXV: UCU) (OTCQX: UURAF) ("Ucore" or the "Company") is pleased to announce the acceptance of its final reporting under Phase 1 of its Other Transaction Agreement ("OTA" or "Agreement") with the US Department of War (the "Reports"). The proprietary Reports were submitted to the US Army Contracting Command - Orlando and included both a Final Demonstration Report and a Final Techno-Economic Assessment ("TEA"). As per the Company's previous press release dated February 17, 2026, the Reports detail the work conducted at Ucore's RapidSX™ Commercialization and Demonstration Facility ("CDF") in Kingston, Ontario, which included direct comparison trials of the patent-pending RapidSX™ technology with conventional solvent extraction ("CSX") over thousands of hours.
The acceptance of the final Reports concludes Ucore's successful performance of Phase 1 under the Agreement and triggers the final Phase 1 payment milestone.
The following excerpt summarizes the Key Performance Metrics outlined in the Reports:
"Table 13 - Key Performance Metrics"
MetricPerformanceREE Separation Processing EfficiencyExtraction RateOn average, 5.4x less mixing time than CSX is needed to achieve target level of extractionSettling RateOn average, 1.8x less settling time than CSX is needed for phase disengagementRecoveryVirtually identical - better than or similar to CSX 13 times out of 14PurityVirtually identical - better than or similar to CSX 11 times out of 14Separation
FlexibilityAble to reconfigure stages in SX circuit within hours, allowing separation of different REEs to different target purities with the same equipmentOntime
FlexibilityAble to start and stop the system at will without loss of production equilibrium. RapidSX™ can immediately restart after planned and unplanned shutdown events.Other Demo Plant Performance DataOperating Hours5,718 hoursTonnage
Processed1.76 metric tonnes REO equivalentSeparations
Applied7 separations: 5 for heavy REE and 2 for light REEFootprintUp to 60% smaller for a process with equal throughputEconomicsCAPEX34% reduction in CAPEXOPEXSimilar: 2.2 $USD/kg of REO feedstock for RapidSX™, a slight decrease from CSX (2.3 $USD/kg)The Phase 1 Reports detail the work completed at the CDF, and provide further support and risk mitigation for the Company's commercialization execution strategy at the Louisiana Strategic Metals Complex ("Louisiana SMC") in Alexandria, Louisiana. Because the proprietary Reports contain detailed technical and commercial analysis provided to the DoW, Ucore is limiting this announcement to a high-level summary with selected tables of the findings most relevant to stakeholders on the Company's path to commercial execution in Louisiana.
Commercial Proof of Performance
The Reports, which were generated from millions of data points generated over a 2-year sequence of campaigns, indicate that the rare earth element ("REE") product recovery and purity achieved with RapidSX™ were consistently equal to or better than CSX. It should be noted that this was the expected result given that the chemistry of RapidSX™ and CSX is exactly the same.
The RapidSX™ advantage is in applying the chemistry much more efficiently, resulting in faster separation steps with a smaller physical equipment footprint. When coupled together, these two attributes yield significant cost and ESG efficiencies across a commercial REE separation facility.
Seven demonstration campaigns were completed as follows, all starting with nearly two tonnes of a heavy mixed rare earth oxide feed source containing both heavy and light REEs:
"Table 6 - Heavy and Light REE Classification of Each Separation"
The success of each of the above separations was determined by comparing the purity and recovery of each separation to the CSX baseline. The purity and recovery values are the key metrics used to compare separation efficiency. Purity is calculated as the amount of target REEs out of total REEs. Recovery is calculated based on the losses to the opposite side of the split.
Operational Flexibility & Lower Capital Intensity
The Reports highlight the ability to stop and restart the system without loss of equilibrium, as well as the ability to reconfigure circuit stages within hours to suit different separations and product objectives. This kind of flexibility is especially important in a commercial refinery, where feed variability, and meeting customer specifications in an evolving Western market, all benefit from a platform that is more agile. The Reports also supports the view that RapidSX™ can apply the proven chemistry of solvent extraction in a smaller and more modular equipment arrangement than conventional mixer-settler systems. Lower SX-area capital intensity can improve project economics, support a staged buildout strategy, and allow capital to be deployed more intelligently as the Louisiana SMC grows.
As noted, the success of the DoW demonstration program was as expected; the Company is not commercializing speculative chemistry. Rather, it is implementing a proven solvent extraction chemistry distribution platform while improving the physical delivery of the process.
"Phase 1 did more than validate a technology platform. It clarified why RapidSX™ matters commercially," said Mike Schrider, P.E., Vice-President and Chief Operating Officer of Ucore. "For Louisiana, the message is straightforward: across seven demonstration campaigns, RapidSX™ matched conventional solvent extraction on purity, recovery, and product quality, while delivering faster extraction and phase disengagement in a smaller operating footprint. We believe that combination is exactly what the U.S. rare earth supply chain needs."
Knowledge Transfer and Copy-and-Paste Deployment
The report emphasizes that continuous improvement, plant learnings, operating protocols, controls development, and sampling discipline are designed to reduce risk for direct knowledge transfer from the Kingston CDF to the Louisiana SMC. The planned coordinated commissioning will shorten the learning curve, strengthen startup discipline, and improve the likelihood of a smoother transition into commercial production.
# # #
About Ucore Rare Metals Inc.
Ucore is focused on rare- and critical-metal resources, extraction, beneficiation, and separation technologies with the potential for production, growth, and scalability. Ucore's vision and plan is to become a leading advanced technology company, providing best-in-class metal separation products and services to the mining and mineral extraction industry.
Through strategic partnerships, this plan includes disrupting the People's Republic of China's control of the North American REE supply chain through the near-term development of a heavy and light rare-earth processing facility in the US State of Louisiana, subsequent SMCs in Canada and Alaska and the longer-term development of Ucore's 100% controlled Bokan-Dotson Ridge Rare Heavy REE Project on Prince of Wales Island in Southeast Alaska, USA ("Bokan").
Ucore is listed on the TSXV under the trading symbol "UCU" and in the United States on the OTC Markets' OTCQX® Best Market under the ticker symbol "UURAF."
For further information, please visit www.ucore.com.
Forward-Looking Statements
This press release includes certain statements that may be deemed "forward-looking statements". All statements in this release (other than statements of historical facts) that address future business development, technological development and/or acquisition activities (including any related required financings), timelines, events, or developments that the Company is pursuing are forward-looking statements. Although the Company believes the expectations expressed in such forward-looking statements are based on reasonable assumptions, such statements are not guarantees of future performance or results, and actual results or developments may differ materially from those in forward-looking statements.
Regarding the disclosure in the press release above about government support for Ucore, the Company has assumed that the applicable projects (including each of the associated milestones) will be completed satisfactorily and in accordance with the respective agreements or letters of intent (as applicable) for such government support. For additional risks and uncertainties regarding the Company, its business activities, its ability to qualify for and receive any additional funding from any U.S. or Canadian government, the CDF and the aforementioned projects (generally), see the risk disclosure in the Company's MD&A for Q4-2025 (filed on SEDAR+ on March 18, 2026) (www.sedarplus.ca) as well as the risks described below.
Regarding the disclosure above in the "About Ucore Rare Metals Inc." section, the Company has assumed that it will be able to procure or retain additional partners and/or suppliers, in addition to Innovation Metals Corp. ("IMC"), as suppliers for Ucore's expected future SMCs. Ucore has also assumed that sufficient external funding will be found to continue and complete the ongoing research and development work required at the CDF and also later prepare a new National Instrument 43-101 technical report that demonstrates that Bokan is feasible and economically viable for the production of both REE and co-product metals and the then prevailing market prices based upon assumed customer offtake agreements. Ucore has also assumed that sufficient external funding will be secured to continue the development of the specific engineering plans for the SMCs and their construction and eventual commissioning and operations. Factors that could cause actual results to differ materially from those in forward-looking statements include, without limitation: IMC failing to protect its intellectual property rights in RapidSX™; RapidSX™ failing to demonstrate commercial viability in large commercial-scale applications; Ucore not being able to procure additional key partners or suppliers for the SMCs; Ucore not being able to raise sufficient funds to fund the specific design and construction of the SMCs and/or the continued development of RapidSX™; adverse capital-market conditions; unexpected due-diligence findings; the emergence of alternative superior metallurgy and metal-separation technologies; the inability of Ucore and/or IMC to retain its key staff members; a change in the legislation in Louisiana or Alaska and/or in the support expressed by the Alaska Industrial Development and Export Authority (AIDEA) regarding the development of Bokan; the availability and procurement of any required interim and/or long-term financing that may be required; and general economic, market or business conditions.
Neither the TSXV nor its Regulation Services Provider (as that term is defined by the TSXV) accept responsibility for the adequacy or accuracy of this release.
CONTACTS
Mr. Michael Schrider, P.E., Ucore Vice President and Chief Operating Officer, is responsible for the content of this news release and may be contacted at 1.902.482.5214.
To view the source version of this press release, please visit https://www.newsfilecorp.com/release/291483
Source: Ucore Rare Metals Inc.
Ready to Announce with Confidence? Send us a message and a member of our TMX Newsfile team will contact you to discuss your needs.
Halifax, Nova Scotia--(Newsfile Corp. - April 14, 2026) - Ucore Rare Metals Inc. (TSXV: UCU) (OTCQX: UURAF) ("Ucore" or the "Company") is pleased to announce the completion of an upgraded mineral resource estimate ("Resource" or "Mineral Resource") for the Bokan Dotson-Ridge rare earth element project in Southeast Alaska ("Bokan"), together with the associated Technical Report (the "Technical Report"). The Technical Report has been prepared in accordance with both National Instrument 43-101 and SEC Regulation S-K 1300.
Halifax, Nova Scotia--(Newsfile Corp. - April 16, 2026) - Ucore Rare Metals Inc. (TSXV: UCU) (OTCQX: UURAF) ("Ucore" or the "Company") is pleased to announce the arrival of a crucial piece of long-lead-time equipment at its Louisiana Strategic Metals Complex ("LA-SMC") in Alexandria, LA. The equipment was procured under the Company's US$22.4 million modified funding agreement with the US Army Contracting Command-Orlando and associated Defense Priorities & Allocations System ("DPAS") Rating. The equipment is a GMM Pfaudler US Inc. 4,000-gallon jacketed glass-lined reactor designed to leach a wide variety of planned Western mixed rare earth oxides ("MREO") and mixed rare earth carbonates ("MREC") to be received at the LA-SMC.
Figure 1 - A 4,000 Gallon Pfaulder Leaching Reactor Arriving at the Louisiana SMC
To view an enhanced version of this graphic, please visit:
https://images.newsfilecorp.com/files/1119/292865_aaf53998745cbbf4_001full.jpg
Ucore presented its DPAS DO-B8 rating in a September 19, 2025, news release and noted that a DPAS rating imposes legal obligations on equipment suppliers, requiring that fulfillment of any LA-SMC order be given preferential treatment over unrated orders to meet national defense and emergency preparedness requirements.
The offloading and placement of the Reactor within the LA-SMC was successfully coordinated by Ucore's selected LA-SMC construction management contractor, Ratcliff Construction of Alexandria, LA. A section of the end wall was removed and replaced to facilitate the placement of the reactor within the building.
"The arrival of this major piece of equipment is a significant milestone for the Ucore Team as we stay laser-focused on establishing commercial rare earth processing in Louisiana," stated Mike Schrider, P.E., Ucore Vice President and Chief Operating Officer. "Ucore is conducting a coordinated knowledge transfer of its RapidSX™ technology platform and ancillary processing systems from its Commercialization and Demonstration Facility [CDF] in Kingston, Ontario, to the LA-SMC. This effort will continue throughout 2026, with the installation of one RapidSX™ Machine scheduled for commissioning and product qualification trials in H1-2027."
Coordinated CDF to LA-SMC activities include:
Anticipated LA-SMC feedstock testing and separation trials at the CDFFactory Acceptance Testing ("FAT") of the RapidSX™ Commercial Scale Equipment Platform at the CDFLA-SMC Engineering, Procurement, and Construction ("EPC") personnel familiarization, design, procurement, construction, and/or testing of the CDF equipment and processesLA-SMC personnel training at the CDF# # #
About Ucore Rare Metals Inc.
Ucore is focused on rare- and critical-metal resources, extraction, beneficiation, and separation technologies with the potential for production, growth, and scalability. Ucore's vision and plan is to become a leading advanced technology company, providing best-in-class metal separation products and services to the mining and mineral extraction industry.
Through strategic partnerships, this plan includes disrupting the People's Republic of China's control of the North American REE supply chain through the near-term development of a heavy and light rare-earth processing facility in the US State of Louisiana, subsequent SMCs in Canada and Alaska and the longer-term development of Ucore's 100% controlled Bokan-Dotson Ridge Rare Heavy REE Project on Prince of Wales Island in Southeast Alaska, USA ("Bokan").
Ucore is listed on the TSXV under the trading symbol "UCU" and in the United States on the OTC Markets' OTCQX® Best Market under the ticker symbol "UURAF."
For further information, please visit www.ucore.com.
Forward-Looking Statements
This press release includes certain statements that may be deemed "forward-looking statements". All statements in this release (other than statements of historical facts) that address future business development, technological development and/or acquisition activities (including any related required financings), timelines, events, or developments that the Company is pursuing are forward-looking statements. Although the Company believes the expectations expressed in such forward-looking statements are based on reasonable assumptions, such statements are not guarantees of future performance or results, and actual results or developments may differ materially from those in forward-looking statements.
Regarding the disclosure in the press release above about government support for Ucore, the Company has assumed that the applicable projects (including each of the associated milestones) will be completed satisfactorily and in accordance with the respective agreements or letters of intent (as applicable) for such government support. For additional risks and uncertainties regarding the Company, its business activities, its ability to qualify for and receive any additional funding from any U.S. or Canadian government, the CDF and the aforementioned projects (generally), see the risk disclosure in the Company's MD&A for Q4-2025 (filed on SEDAR+ on March 18, 2026) (www.sedarplus.ca) as well as the risks described below.
Regarding the disclosure above in the "About Ucore Rare Metals Inc." section, the Company has assumed that it will be able to procure or retain additional partners and/or suppliers, in addition to Innovation Metals Corp. ("IMC"), as suppliers for Ucore's expected future SMCs. Ucore has also assumed that sufficient external funding will be found to continue and complete the ongoing research and development work required at the CDF and also later prepare a new National Instrument 43-101 technical report that demonstrates that Bokan is feasible and economically viable for the production of both REE and co-product metals and the then prevailing market prices based upon assumed customer offtake agreements. Ucore has also assumed that sufficient external funding will be secured to continue the development of the specific engineering plans for the SMCs and their construction and eventual commissioning and operations. Factors that could cause actual results to differ materially from those in forward-looking statements include, without limitation: IMC failing to protect its intellectual property rights in RapidSX™; RapidSX™ failing to demonstrate commercial viability in large commercial-scale applications; Ucore not being able to procure additional key partners or suppliers for the SMCs; Ucore not being able to raise sufficient funds to fund the specific design and construction of the SMCs and/or the continued development of RapidSX™; adverse capital-market conditions; unexpected due-diligence findings; the emergence of alternative superior metallurgy and metal-separation technologies; the inability of Ucore and/or IMC to retain its key staff members; a change in the legislation in Louisiana or Alaska and/or in the support expressed by the Alaska Industrial Development and Export Authority (AIDEA) regarding the development of Bokan; the availability and procurement of any required interim and/or long-term financing that may be required; and general economic, market or business conditions.
Neither the TSXV nor its Regulation Services Provider (as that term is defined by the TSXV) accept responsibility for the adequacy or accuracy of this release.
CONTACTS
Mr. Michael Schrider, P.E., Ucore Vice President and Chief Operating Officer, is responsible for the content of this news release and may be contacted at 1.902.482.5214.
To view the source version of this press release, please visit https://www.newsfilecorp.com/release/292865
Source: Ucore Rare Metals Inc.
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Halifax, Nova Scotia--(Newsfile Corp. - April 27, 2026) - Ucore Rare Metals Inc. (TSXV: UCU) (OTCQX: UURAF) ("Ucore" or the "Company") advises that an aggregate of 2,775,000 options have been granted to directors, officers, employees and consultants of the Company, subject to the approval of the TSX Venture Exchange. The options are exercisable into common shares at a price of $5.33 per share and the options expire five years from April 27, 2026, the date of grant. One third of the options will vest after six months, with one third vesting every six months thereafter until fully vested.
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About Ucore Rare Metals Inc.
Ucore is focused on rare- and critical-metal resources, extraction, beneficiation, and separation technologies with the potential for production, growth, and scalability. Ucore's vision and plan is to become a leading advanced technology company, providing best-in-class metal separation products and services to the mining and mineral extraction industry.
Through strategic partnerships, this plan includes disrupting the People's Republic of China's control of the North American REE supply chain through the near-term development of a heavy and light rare-earth processing facility in the US State of Louisiana, subsequent SMCs in Canada and Alaska and the longer-term development of Ucore's 100% controlled Bokan-Dotson Ridge Rare Heavy REE Project on Prince of Wales Island in Southeast Alaska, USA ("Bokan").
Ucore is listed on the TSXV under the trading symbol "UCU" and in the United States on the OTC Markets' OTCQX® Best Market under the ticker symbol "UURAF."
For further information, please visit www.ucore.com.
Forward-Looking Statements
This press release includes certain statements that may be deemed "forward-looking statements". All statements in this release (other than statements of historical facts) that address future business development, technological development and/or acquisition activities (including any related required financings), timelines, events, or developments that the Company is pursuing are forward-looking statements. Although the Company believes the expectations expressed in such forward-looking statements are based on reasonable assumptions, such statements are not guarantees of future performance or results, and actual results or developments may differ materially from those in forward-looking statements.
For additional risks and uncertainties regarding the Company, its business activities, its ability to qualify for and receive any additional funding from any U.S. or Canadian government, the CDF and the aforementioned projects (generally), see the risk disclosure in the Company's MD&A for Q4-2025 (filed on SEDAR+ on March 18, 2026) (www.sedarplus.ca) as well as the risks described below.
Regarding the disclosure above in the "About Ucore Rare Metals Inc." section, the Company has assumed that it will be able to procure or retain additional partners and/or suppliers, in addition to Innovation Metals Corp. ("IMC"), as suppliers for Ucore's expected future SMCs. Ucore has also assumed that sufficient external funding will be found to continue and complete the ongoing research and development work required at the CDF and also later prepare a new National Instrument 43-101 technical report that demonstrates that Bokan is feasible and economically viable for the production of both REE and co-product metals and the then prevailing market prices based upon assumed customer offtake agreements. Ucore has also assumed that sufficient external funding will be secured to continue the development of the specific engineering plans for the SMCs and their construction and eventual commissioning and operations. Factors that could cause actual results to differ materially from those in forward-looking statements include, without limitation: IMC failing to protect its intellectual property rights in RapidSX™; RapidSX™ failing to demonstrate commercial viability in large commercial-scale applications; Ucore not being able to procure additional key partners or suppliers for the SMCs; Ucore not being able to raise sufficient funds to fund the specific design and construction of the SMCs and/or the continued development of RapidSX™; adverse capital-market conditions; unexpected due-diligence findings; the emergence of alternative superior metallurgy and metal-separation technologies; the inability of Ucore and/or IMC to retain its key staff members; a change in the legislation in Louisiana or Alaska and/or in the support expressed by the Alaska Industrial Development and Export Authority (AIDEA) regarding the development of Bokan; the availability and procurement of any required interim and/or long-term financing that may be required; and general economic, market or business conditions.
Neither the TSXV nor its Regulation Services Provider (as that term is defined by the TSXV) accept responsibility for the adequacy or accuracy of this release.
To view the source version of this press release, please visit https://www.newsfilecorp.com/release/294386
Source: Ucore Rare Metals Inc.
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Companies mentioned: Greenland Mines Ltd. (NASDAQ: GRML), Neo Performance Materials Inc. (TSX: NEO; OTCQX: NOPMF), USA Rare Earth Inc. (NASDAQ: USAR), Ucore Rare Metals Inc. (TSXV: UCU; OTCQX: UURAF), Lynas Rare Earths Ltd. (ASX: LYC), American Rare Earths Limited (ASX: ARR; OTCQX: ARRNF)
AMERICAN NEWS GROUP News Commentary
, /PRNewswire/ -- If you're a retail investor trying to find an entry point into the rare earth boom, this deal is one worth paying attention to.
Key Takeaways
Greenland Mines Ltd. (NASDAQ: GRML) just secured one of the most strategically located rare earth projects in the Western world through a US$35 million agreement with Neo Performance Materials. The Sarfartoq Carbonatite Complex in southwest Greenland is rich in neodymium and praseodymium — the two rare earths most needed for permanent magnets used in EVs, wind turbines, and defense systems. Neo Performance Materials is staying on as a long-term partner, keeping an equity stake in Greenland Mines and the right to purchase up to 60% of the project's future output. Greenland Mines now has two world-class projects: the Skaergaard palladium-gold-platinum deposit and the Sarfartoq rare earth project — both in stable, Western-aligned Greenland. China still controls roughly 61% of global rare earth mining and 91% of refining, making Western-jurisdiction projects like Sarfartoq strategically important for governments and manufacturers alike.
The Deal in Plain English
Greenland Mines Ltd. (NASDAQ: GRML) just signed an agreement to take over the Sarfartoq rare earth project in southwest Greenland from Neo Performance Materials Inc. (TSX: NEO; OTCQX: NOPMF). The price tag is US$35 million — US$20 million in cash, and US$15 million in Greenland Mines stock. [1]
Here is what makes this stand out for retail investors:
Neo Performance Materials is not exiting the project. They are keeping an equity stake in Greenland Mines and the right to buy up to 60% of the ore that comes out of Sarfartoq under an existing offtake arrangement. [1] That means Neo, a real revenue-generating company that just reported Q1 2026 revenue of about US$155 million, is essentially saying it wants Greenland Mines to advance this project — and plans to be the main customer. [2] For a small-cap developer, this is the kind of validation that most companies spend years trying to get. Why the Sarfartoq Project Is a Big Deal
Rare earth projects are not all created equal. Sarfartoq has three things going for it that retail investors should understand.
1. The Right Minerals
Sarfartoq is rich in neodymium and praseodymium, which together make up roughly 25% to 40% of the total rare earth oxides on the property. [3] These two elements are the workhorses of the rare earth magnet industry. They are what makes electric vehicle motors small, light, and powerful. They are also what makes wind turbine generators efficient enough to compete with traditional power sources.
2. The Right Location
Most undeveloped rare earth projects are in the middle of nowhere. Sarfartoq is different. It is located about 60 kilometers from an international airport, has access to tidewater and a major port facility, and is close to some of the best hydroelectric power potential in Greenland. [3] That kind of infrastructure access can knock years off a project's development timeline.
3. The Right Jurisdiction
Greenland is a Western-aligned territory of the Kingdom of Denmark. The Government of Greenland has made critical minerals a priority for economic development. The transfer of the NNSR shares is subject to government approval under the Greenland Mineral Activities Act, but Greenland has already approved a similar transfer for this same project in 2023. [3] That historical track record matters.
The Bigger Picture: Why Rare Earths Are Hot Again
China still controls roughly 61% of the world's rare earth mining and 91% of refining capacity, according to the International Energy Agency. [4] In 2025, Beijing introduced two waves of export controls on rare earths. Some of those controls were temporarily suspended in November 2025 after a U.S.-China trade truce, but the licensing system for seven key elements remains in place. [4]
The result is that prices for heavy rare earths outside of China have climbed, and Western governments are pouring money into building alternative supply chains. The U.S. Department of Defense has already committed more than US$439 million to domestic rare earth projects, and Canada, Europe, and Australia are doing the same. [5]
Four Other Names Riding the Same Wave
Greenland Mines is one of several public companies positioning to feed the Western rare earth supply chain. For retail investors building a watchlist, here are four others to know.
USA Rare Earth Inc. (NASDAQ: USAR)
USA Rare Earth is building a domestic mine-to-magnet supply chain in the United States. The company is developing the Round Top project in Texas, which hosts heavy rare earths needed for high-performance magnets, and runs a magnet manufacturing facility in Stillwater, Oklahoma. [6] In April 2026, USA Rare Earth announced an agreement to acquire Serra Verde, the owner of the only scaled rare earth mine outside of Asia producing all four magnetic rare earths — a transaction with an implied equity value of roughly US$2.8 billion. [7]
Ucore Rare Metals Inc. (TSXV: UCU; OTCQX: UURAF)
Ucore is a smaller-cap Canadian company that is building a Strategic Metals Complex in Alexandria, Louisiana, using its own RapidSX rare earth separation technology. The first phase is targeting about 2,000 tonnes per year of separated rare earth oxides by 2026, with later phases scaling up significantly. [8] The U.S. Department of Defense has been backing Ucore's separation technology, making the company one of the more closely watched processing plays in the sector.
Lynas Rare Earths Ltd. (ASX: LYC)
Lynas is the largest rare earth producer outside of China and has been operating profitably for years. The company mines rare earths at Mt Weld in Western Australia and processes them at facilities in Malaysia, with new processing capacity coming online in the United States. Lynas serves as a benchmark for what a fully built-out, Western-aligned rare earth supply chain looks like — and a reminder of how much room there is for new entrants given how dominant China remains.
American Rare Earths Limited (ASX: ARR; OTCQX: ARRNF)
American Rare Earths is advancing the Halleck Creek project in Wyoming, which the company describes as one of the largest rare earth deposits in North America. With U.S. defense procurement rules increasingly excluding Chinese material, projects like Halleck Creek are positioned to benefit directly from federal funding programs and offtake support.
What This Means for the Average Investor
Most retail investors will never get the chance to invest at the ground floor of a true critical minerals deal. The big rare earth producers — Lynas, MP Materials — already trade at multi-billion-dollar valuations. The earlier-stage developers offer more upside but come with more risk.
What sets Greenland Mines Ltd. (NASDAQ: GRML) apart in this group is the combination of a Nasdaq listing, a partnership with a real revenue-generating company (Neo), a project in a stable Western jurisdiction, and now two world-class assets in Greenland.
For investors who already missed the big run-ups in MP Materials and USA Rare Earth, deals like this one are exactly the kind of catalyst worth tracking. Always do your own research, understand the risks, and never invest more than you can afford to lose.
DISCLAIMER: Nothing in this publication should be considered as personalized financial advice. We are not licensed under securities laws to address your particular financial situation. No communication by our employees to you should be deemed as personalized financial advice. Please consult a licensed financial advisor before making any investment decision. This is a paid advertisement and is neither an offer nor recommendation to buy or sell any security. We hold no investment licenses and are thus neither licensed nor qualified to provide investment advice. The content in this report or email is not provided to any individual with a view toward their individual circumstances. americannewsgroup.com is a wholly-owned subsidiary of Market IQ Media Group, Inc. ("MIQ"). MIQ has been paid a fee for Greenland Mines Corp. advertising and digital media from Creative Direct Marketing Group ("CDMG"). There may be 3rd parties who may have shares of Greenland Mines Corp., and may liquidate their shares which could have a negative effect on the price of the stock. This compensation constitutes a conflict of interest as to our ability to remain objective in our communication regarding the profiled company. Because of this conflict, individuals are strongly encouraged to not use this publication as the basis for any investment decision. The owner/operator of MIQ does not own any shares of Greenland Mines Corp. but reserve the right to buy and sell, and will buy and sell shares of Greenland Mines Corp. at any time without any further notice commencing immediately and ongoing. We also expect further compensation as an ongoing digital media effort to increase visibility for the company, no further notice will be given, but let this disclaimer serve as notice that all material, including this article, which is disseminated by MIQ has been reviewed and approved on behalf of Greenland Mines Corp. by CDMG. While all information is believed to be reliable, it is not guaranteed by us to be accurate. Individuals should assume that all information contained in our newsletter is not trustworthy unless verified by their own independent research. Also, because events and circumstances frequently do not occur as expected, there will likely be differences between any predictions and actual results. Always consult a licensed investment professional before making any investment decision. Be extremely careful, investing in securities carries a high degree of risk; you may likely lose some or all of the investment.
CAUTIONARY NOTE REGARDING MINERAL RESOURCES:
The Mineral Resource Estimates referenced in this article were prepared in accordance with NI 43-101 by SLR Consulting as disclosed in the technical report dated November 22, 2022. Mineral Resources are not Mineral Reserves and do not have demonstrated economic viability. The gross undiscounted in-situ metal values expressed herein are illustrative calculations using February 2026 metal prices and do not account for mining recoveries, metallurgical losses, capital costs, operating costs, royalties, taxes, permitting requirements, or any other technical or economic factors. These values are not indicative of future revenue, project economics or net present value. No preliminary economic assessment, pre-feasibility study, or feasibility study has been completed on the Skaergaard Project, and there is no certainty that the Mineral Resources disclosed will be converted to Mineral Reserves or that an economically viable mining operation can be established.
FORWARD-LOOKING STATEMENTS:
This publication contains forward-looking information which is subject to a variety of risks and uncertainties and other factors that could cause actual events or results to differ from those projected in the forward-looking statements. Forward-looking statements in this publication include that demand for platinum group metals and critical minerals will continue to grow and tighten; that Greenland Mines Ltd's Skaergaard Project will advance through its planned technical, metallurgical, and environmental work programs as described; that the Company's engagements with SLR Consulting, GTK Mintec, and WSP will proceed as planned; that the Iceland LOI will progress toward a binding agreement with the cost and savings characteristics described; that comparable companies will perform as expected. The forward-looking information contained herein is provided for the purpose of assisting the reader to understand the Company's business, however such information may not be appropriate for other purposes. Risks that could change or prevent these statements from coming to fruition include changing governmental laws and policies; permitting risks; the Company's ability to obtain and retain necessary licensing; political and competitive risks; failure of forecasts and assumptions to come to fruition; metal price volatility; the inherent uncertainty of mineral resource estimates; and other unforeseen circumstances. The publisher of this article does not take responsibility for the accuracy of any statements made by the issuing company or its representatives. Readers are cautioned not to place undue reliance on these forward-looking statements, and the publisher undertakes no obligation to update or revise any forward-looking statements except as required by applicable law.
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Orbital Engineering, Inc.'s Louisiana SMC report supports:
a three production-line RapidSX™ configuration targeted to process up to ≈9,000 tpa of TREO contained in qualified rare earth feedstocks, eliminating the fourth production line as originally considered.
the production of a full rare earth product suite, including NdPr, Pr, Nd, Sm, Gd, Tb and Dy, noted by the U.S. DoW as most crucial under their Defense Production Act and IBAS Programs.
incorporating the principles of lean manufacturing with fewer parallel production lines, yielding fewer individual column stages, resulting in reduced maintenance points, less operator time, and other operating cost efficiencies, yet with similar processing throughput.
the creation of an additional ≈600 tpa TREO capacity, multi-purpose RapidSX™ Machine "A" to be constructed first under the DoW Phase 2 Project, allowing for broader product flexibility, production line integration, and simplified execution.
Halifax, Nova Scotia--(Newsfile Corp. - May 28, 2026) - Ucore Rare Metals Inc. (TSXV: UCU) (OTCQX: UURAF) ("Ucore" or the "Company") is pleased to announce the results of a CAPEX and Capacity Engineering Report, dated May 27, 2026, prepared by the Company's engineering consortium and led by Orbital Engineering, Inc. ("Orbital"). This report reflects the efforts to move from the Company's Kingston, Ontario, Commercialization and Demonstration Facility ("CDF") to Production Line 1 at the Louisiana Strategic Metals Complex ("SMC"). Details include engineered capital expenditure ("CAPEX") and capacity projections for the initial standalone Machine A, and its planned integration into the first multi-machine RapidSX™ Production Line[1] ("Production Line 1") at the Louisiana SMC.
Optimized Louisiana SMC Configuration
As a result of efficiencies identified through engineering, demonstration, and scale-up work testing, Ucore is designing the Louisiana SMC to consist of the initial ≈600 tonnes per annum ("tpa") total rare earth oxide ("TREO") Machine A plus three RapidSX™ Production Lines (or "Trains"), each capable of processing up to ≈3,000 tpa of TREO. This optimized configuration reduces the planned number of production lines from four to three, while targeting an overall Louisiana SMC throughput capacity of ≈9,600 tpa of TREO. This configuration better balances capital intensity, reliability, maintainability, commercial flexibility, and operating cost per unit of production.
Each machine will use optimized RapidSX™ columns and supporting equipment throughout, increasing upfront capital costs but improving long-term operating economics by reducing the number of parallel processing lines, individual columns, pumps, valves, instruments, and maintenance points, and lowering operator time per unit of production.
"After approximately 6,500+ run-time hours in Ucore's RapidSX™ Commercialization and Demonstration Facility, our engineering team has developed a commercial configuration that is expected to lower unit operating costs and improve reliability over the life of the plant with expanded initial investment," stated Pat Ryan, P.Eng., Chairman and CEO of Ucore. "This is an important evolution in the Louisiana SMC plan. We are moving from a lowest initial build-cost concept toward a more robust commercial operating configuration designed for higher throughput per production line, fewer production lines, fewer maintenance points, and better long-term operating performance."
Mike Schrider, P.E., Vice President and Chief Operating Officer of Ucore, commented: "The engineering objective has been to translate RapidSX™ demonstration work into a commercial configuration that is practical to build, practical to operate, and scalable for North American rare earth supply chain requirements. The optimized design is intended to reduce process complexity while retaining Ucore's ability to process qualified feedstocks from multiple independent rare earth sources."
Pending construction completion, commissioning, qualification, and receipt of all required funding and permits, Ucore's Louisiana SMC shall be capable of accepting mixed rare earth carbonate ("MREC") and mixed rare earth oxide ("MREO") from Western-friendly feedstock sources and processing up to ≈9,600 tpa of contained TREOs. The SMC is designed to take advantage of the inherent flexibility and modularity of the RapidSX™ technical platform and capable of producing NdPr, Pr, Nd, Sm, Gd, SmEuGd ("SEG"), Tb, Dy, rare earth oxide products, and intermediates.
Enhancements to Standalone Machine A
The first RapidSX™ machine to be deployed in Louisiana, Machine A, is to be partially funded through the Company's previously announced US$18.4 million funding agreement with the US Department of War (see Ucore Press Release dated July 14, 2025). Originally contemplated as a single machine with 64 RapidSX™ stages and designed to replicate the 'any split' methodology demonstrated at the CDF through intermediate product storage and machine reuse, the now enhanced Machine A will consist of ≈118 RapidSX™ stages. This will allow for the direct production of neodymium-praseodymium ("NdPr") from conventional MREC or MREO feedstocks, as well as praseodymium ("Pr"), neodymium ("Nd"), samarium ("Sm"), gadolinium ("Gd"), terbium ("Tb"), and/or dysprosium ("Dy") from select partial MREC product groups without the use of interim product holding tanks for successive separations. This important strategic adjustment was in direct response to feedback from North American defense contractors regarding their urgent need to secure Western sources of these critical oxides.
Combining Machine A with Production Line #1
Upon successful operation and completion of gating items associated with Machine A, the Company intends to construct RapidSX™ Machines #1 and #2 of Production Line 1, dedicated to processing up to 3,000 tpa of TREO to produce an NdPr product. At the same time, Machine A will have the ability to work independently or attach to the back end of Production Line 1 to produce a SEG[2] product, while subsequent Production Lines 2 and 3 will be installed to eventually broaden the SMC's multi-product suite of offerings.
Planned Production Scale-Up
Ucore's Louisiana SMC facility scale-up is proceeding under a defined execution plan:
Deployment stepScope
ProductsEnhanced Machine AThe first RapidSX™ commercial machine capable of up to ≈600 tpa TREO of bespoke processingNdPr at an estimated throughput of ≈600 tpa TREO, with the ability to also produce Pr, Nd, Sm, Gd, Tb, and/or Dy, depending on feedstock and sub-products availabilityProduction Line 1Two RapidSX™ machines of ≈3,000 tpa TREO throughputNdPr production with the remaining products feeding Production Line 2Enhanced Machine A - IntegrationMachine A can be integrated into Production Line 1 Capable of producing a SEG product sub-groupProduction Line 2Five RapidSX™ machines ≈3,000 tpa TREO throughputNdPr, Tb, Dy, and SEG. Machines #3, #4 and #5 will be sized to accept intermediate streams from Production Lines 1 and 3Production Line 3Two RapidSX™ machines ≈3,000 tpa TREO throughputNdPr production with the remaining products feeding Production Line 2Engineered Capital Cost Estimates
Orbital's engineered capital cost estimate for the Enhanced Machine A and Production Line 1 is as follows:
Item
Engineered Capital Cost EstimateEnhanced Machine A
US$60MProduction Line 1US$44MOxide Production and PackagingUS$31MMachine A and Production Line 1 - Cumulative CostUS$135MThe updated capital plan reflects the Company's move from a lower initial build-cost configuration to a more robust configuration designed to lower long-term unit operating costs, improve process reliability, and increase maintainability as the Louisiana SMC scales toward commercial operations. The updated estimates also reflect inflation and market-cost escalation since the prior pre-engineering estimates, as well as the expansion of commercial-scale oxide production and packaging equipment with more substantive supporting infrastructure and higher-capacity systems.
As mentioned above, the US$60 million estimated capital cost of Enhanced Machine A will be partially funded by the previously announced US$18.4 million funding agreement with the US Department of War. The amounts in the table above do not include the cost of the first-fill of prospective feedstocks. The estimated timeline for completing the installation, testing, and commissioning of Machine A remains H1-2027.
Rare Earth Market Conditions
Market prices for rare earth oxides sold outside of China continue to reflect constrained Western supply chains and strong demand for critical magnet materials. According to Benchmark Mineral Intelligence's Rare Earths Price Assessment (30th April 2026), selected rare earth oxide prices were as follows:
ProductChina priceIndicative ex-China priceNdPr oxideUS$116 / kgUS$119 / kgTb oxideUS$890 / kgUpwards of 5x DDP ChinaDy oxideUS$200 / kgUpwards of 7x DDP ChinaThe markets for samarium and gadolinium remain more opaque, with fewer published data points available. However, the Company's trading partners have anecdotally observed samarium and gadolinium each trading outside of China at more than US$300 per kg. The Company cautions that these indicative and anecdotal pricing observations may not be representative of realized sales prices, which will depend on product specification, jurisdiction, customer qualification, contract terms, volume, delivery timing, and other commercial factors.
Canadian SMC Update
The Company remains engaged with Canadian federal government officials regarding the Company's proposed Canadian rare earth processing facility and the conditional funding package of up to C$36.3 million announced by Ucore on October 31, 2025. Ucore looks forward to providing further details to stakeholders as they become available in the coming months.
About Ucore Rare Metals Inc.
Ucore is advancing North American rare earth separation and refining through its Louisiana Strategic Metals Complex and the commercialization of its RapidSX™ separation technology. Ucore's vision is to become a leading advanced technology company providing metal separation products and services to the mining and mineral extraction industry.
Through strategic partnerships, Ucore's plan includes the development of a heavy and light rare earth processing facility in the United States, subsequent Strategic Metals Complexes in Canada and Alaska, and the longer-term development of Ucore's 100%-controlled Bokan-Dotson Ridge Rare Heavy REE Project on Prince of Wales Island in Southeast Alaska, USA.
Ucore is listed on the TSX Venture Exchange under the trading symbol "UCU" and in the United States on the OTC Markets' OTCQX® Best Market under the ticker symbol "UURAF."
Forward-Looking Statements
This press release contains "forward-looking information" and "forward-looking statements" (collectively, "forward-looking statements") within the meaning of applicable Canadian securities laws. All statements in this release, other than statements of historical fact, that address future business development, technological development, engineering, procurement, construction, commissioning, commercial production, operating costs, capital costs, project timelines, throughput, product mix, feedstock processing, government funding, customer qualification, offtake, market prices, or other future events or developments are forward-looking statements.
Forward-looking statements in this release includes, without limitation, statements regarding: the design, configuration and development of the Louisiana SMC; the expected number of RapidSX™ production lines and machines; expected throughput of 9,600 tonnes per annum of TREO; expected production of NdPr, Nd, Pr, Sm, Gd, Tb, and Dy; the expected sequencing and timing of t Machine A, Production Line 1, Production Line 2, and Production Line 3; estimated capital costs for Machine A and Production Line 1 and related infrastructure; expected operating characteristics, including potential reductions in unit operating costs and improvements in reliability; targeted milestones for engineering, construction, commissioning and commercial production; availability and sourcing of feedstock; customer engagement and potential product demand; rare earth market conditions and pricing; and the potential receipt of government funding and other financing..
Forward-looking statements are based on a number of material assumptions, including, without limitation: the successful completion and accuracy of baseline, front-end-engineering design and detailed engineering studies; the ability to complete further engineering, procurement, and construction activities as currently contemplated; the availability, cost, and timely delivery of equipment, materials, utilities, labour and construction services; the Company's ability to secure sufficient financing on acceptable terms; the receipt and timing of all required permits and approvals; the successful scale-up and commercial deployment of RapidSX™ technology from demonstration to commercial operation; the availability of qualified feedstock from third-party suppliers; successful customer qualification and offtake discussions; continued support from governmental partners; and general economic, market, and industry conditions, including assumptions regarding rare earth oxide prices, which are subject to significant volatility..
Forward-looking information relating to capital cost estimates and project design is based on a baseline engineering report and remains subject to refinement through further engineering and project development. Such estimates may not be directly comparable to previously disclosed estimates, which were prepared at an earlier stage of project development and may have included different scope elements, assumptions, or cost categories, including feedstock, working capital, or other non-capital items.
In addition, statements regarding expected operating efficiencies, cost reductions, reliability, and commercial performance are based on current engineering assumptions and preliminary analyses and are subject to validation through commissioning and commercial operations. There can be no assurance that such expectations will be achieved in whole or in part.
Although the Company believes that the assumptions underlying the forward-looking information are reasonable, there can be no assurance that such assumptions will prove to be accurate or that the anticipated results, performance, or achievements will be realized. Actual results may differ materially from those expressed or implied by the forward-looking information.
Factors that could cause actual results to differ materially include, without limitation: risks associated with the development, scale-up, and commercialization of new or unproven technologies; the risk that RapidSX™ may not perform at commercial scale as expected; engineering design changes; inaccuracies in capital or operating cost estimates; cost escalation due to inflation, supply chain disruption, or market conditions; delays or failures in procurement, construction, or commissioning; the inability to obtain or maintain required permits, approvals, or regulatory authorizations; challenges in securing adequate financing; adverse capital market conditions; variability in feedstock supply, quality, or pricing; failure to secure or maintain commercial relationships, customer qualification, or offtake arrangements; fluctuations and uncertainty in rare earth oxide prices and demand; the risk that indicative or quoted market prices, including for ex-China markets, may not be realized; operational risks once in production, including equipment failures or lower-than-expected recoveries; geopolitical risk; changes in applicable laws or regulations; environmental or permitting challenges; loss of key personnel; and general economic, business, or competitive conditions.
Readers are cautioned not to place undue reliance on forward-looking statements. The Company undertakes no obligation to update forward-looking statements except as required by applicable securities laws.
Neither the TSX Venture Exchange nor its Regulation Services Provider accepts responsibility for the adequacy or accuracy of this release.
[1] A RapidSX™ Production line is a series of RapidSX™ Machines (each machine conducts a specific solvent extraction chemistry split) working together to produce multiple separated products.
[2] Samarium, Europium and Gadolinium.
To view the source version of this press release, please visit https://www.newsfilecorp.com/release/299208
Source: Ucore Rare Metals Inc.
Ready to Announce with Confidence? Send us a message and a member of our TMX Newsfile team will contact you to discuss your needs.
Halifax, Nova Scotia--(Newsfile Corp. - June 1, 2026) - Ucore Rare Metals Inc. (TSXV: UCU) (OTCQX: UURAF) ("Ucore" or the "Company") is pleased to announce a significant step forward in Canada's critical minerals strategy, having hosted senior officials from Natural Resources Canada ("NRCan") and other Government of Canada departments at its Commercialization and Demonstration Facility ("CDF") in Kingston, Ontario, on May 14, 2026. The high-level visit focused on Ucore's progress under Natural Resources Canada's Critical Minerals Research, Development and Demonstration ("CMRDD") program, and other federal initiatives to strengthen domestic rare earth element ("REE") supply chains.
During the visit, Ucore showcased the Company's advancements in REE separation using its patent pending RapidSX™ technology. Funding from the CMRDD program is advancing the Technology Readiness Level ("TRL") of Ucore's RapidSX™ technology platform through the production of neodymium-praseodymium ("NdPr") and Samarium ("Sm") products at the CDF from tonnes of Canada-friendly feedstock sources.
Discussions also explored the implementation of new policies supporting Canadian critical mineral independence and the standing up of the recently established $2 billion Critical Minerals Sovereign Fund.
Mike Schrider, P.E., Ucore's Vice President & Chief Operating Officer, emphasized the growing momentum behind the Company's Canadian operations:
"Our Kingston team has made demonstrable progress under the NRCan CMRDD program, continuing to prove the efficacy of RapidSX™ as a commercial-ready solution for the separation of both heavy and light rare earth elements. Hosting NRCan and other senior officials at our facility allowed us to show, firsthand, how we are turning policy into practice."
Dr. Ahmad Hussein, Head of External Affairs and Ucore's Advisory Board Member, highlighted the technical and strategic alignment with federal priorities:
"The visit confirmed that Ucore's work directly supports Canada's mandate to build secure, sustainable rare earth supply chains. Our progress in REE processing at the Kingston facility demonstrates the viability of on-shore separation. We are actively reviewing how the $2 billion Critical Minerals Sovereign Fund and new policy frameworks can be leveraged to scale our operations, reduce foreign dependency, and deliver long-term value for Canadian industry."
The RapidSX™ Commercialization and Demonstration Facility is the centerpiece of Ucore's Canadian strategy, positioning the Company as a key enabler of North American rare earth production. Ucore continues to work closely with federal partners to advance towards full commercial deployment in Canada.
.# # #
About Ucore Rare Metals Inc.
Ucore is focused on rare and critical-metal resources, extraction, beneficiation, and separation technologies with the potential for production, growth, and scalability. Ucore's vision and plan is to become a leading advanced technology company, providing best-inclass metal separation products and services to the mining and mineral extraction industry.
Through strategic partnerships, this plan includes disrupting the People's Republic of China's control of the North American REE supply chain through the near-term development of a heavy and light rare-earth processing facility in the US State of Louisiana, subsequent SMCs in Canada and Alaska and the longer-term development of Ucore's 100% controlled BokanDotson Ridge Rare Heavy REE Project on Prince of Wales Island in Southeast Alaska, USA ("Bokan").
Ucore is listed on the TSXV under the trading symbol "UCU" and in the United States on the OTC Markets' OTCQX® Best Market under the ticker symbol "UURAF."
For further information, please visit www.ucore.com.
Forward-Looking Statements
This press release includes certain statements that may be deemed "forward-looking statements". All statements in this release (other than statements of historical facts) that address future business development, technological development and/or acquisition activities (including any related required financings), timelines, events, or developments that the Company is pursuing are forward-looking statements. Although the Company believes the expectations expressed in such forward-looking statements are based on reasonable assumptions, such statements are not guarantees of future performance or results, and actual results or developments may differ materially from those in forward-looking statements.
Regarding the disclosure in the press release above about government support for Ucore, the Company has assumed that the applicable projects (including each of the associated milestones) will be completed satisfactorily and in accordance with the respective agreements or letters of intent (as applicable) for such government support. For additional risks and uncertainties regarding the Company, its business activities, its ability to qualify for and receive any additional funding from any U.S. or Canadian government, the CDF and the aforementioned projects (generally), see the risk disclosure in the Company's MD&A for Q1-2026 (filed on SEDAR+ on May 29, 2026) (www.sedarplus.ca) as well as the risks described below.
Regarding the disclosure above in the "About Ucore Rare Metals Inc." section, the Company has assumed that it will be able to procure or retain additional partners and/or suppliers, in addition to Innovation Metals Corp. ("IMC"), as supply chain participants for Ucore's expected future SMCs. Ucore has also assumed that sufficient external funding will be found to continue and complete the ongoing research and development work required at the CDF and also later prepare a new National Instrument 43-101 technical report that demonstrates that Bokan is feasible and economically viable for the production of both REE and co-product metals and the then prevailing market prices based upon assumed customer offtake agreements. Ucore has also assumed that sufficient external funding will be secured to continue the development of the specific engineering plans for the SMCs and their construction and eventual commissioning and operations. Factors that could cause actual results to differ materially from those in forward-looking statements include, without limitation: IMC failing to protect its intellectual property rights in RapidSX™; RapidSX™ failing to demonstrate commercial viability in large commercial-scale applications; Ucore not being able to procure additional key partners or suppliers for the SMCs; Ucore not being able to raise sufficient funds to fund the specific design and construction of the SMCs and/or the continued development of RapidSX™; unexpected cost overruns; adverse capital-market conditions; unexpected due-diligence findings; the emergence of alternative superior metallurgy and metal-separation technologies; the inability of Ucore and/or IMC to retain its key staff members; a change in the legislation in Louisiana or Alaska and/or in the support expressed by the Alaska Industrial Development and Export Authority (AIDEA) regarding the development of Bokan; the availability and procurement of any required interim and/or long-term financing that may be required; and general economic, market or business conditions.
Neither the TSXV nor its Regulation Services Provider (as that term is defined by the TSXV) accept responsibility for the adequacy or accuracy of this release.
CONTACTS
Mr. Michael Schrider, P.E., Ucore Vice President and Chief Operating Officer, is responsible for the content of this news release and may be contacted at 1.902.482.5214.
For additional information, please contact:
Mark MacDonald
Vice President, Investor Relations
Ucore Rare Metals Inc.
1.902.482.5214 [email protected]
To view the source version of this press release, please visit https://www.newsfilecorp.com/release/299616
Source: Ucore Rare Metals Inc.
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OMAHA, NE, March 30, 2026 (GLOBE NEWSWIRE) -- FitLife Brands, Inc. (“FitLife,” or the “Company”) (Nasdaq: FTLF), a provider of innovative and proprietary nutritional supplements and wellness products, today announced that it plans to report its financial performance for the fourth quarter of fiscal 2025 on Tuesday, March 31, 2026.
In addition, the Company announced that it will hold an investor conference call after market close on April 1, 2026 at 4:30 pm ET. Investors interested in participating in the live call can dial (833) 492-0064 from the U.S. and provide the conference identification code of 115536. International participants can dial (973) 528-0163 and provide the same code.
About FitLife Brands
FitLife Brands is a developer and marketer of innovative and proprietary nutritional supplements and wellness products for health-conscious consumers. FitLife markets over 500 different products online and through various retail locations. FitLife is headquartered in Omaha, Nebraska. For more information, please visit our website at www.fitlifebrands.com.
OMAHA, NE, April 01, 2026 (GLOBE NEWSWIRE) -- FitLife Brands, Inc. (“FitLife” or the “Company”) (NASDAQ: FTLF), a provider of innovative and proprietary nutritional supplements and wellness products, today announced financial results for the fourth quarter and full year ended December 31, 2025.
Highlights for the fourth quarter ended December 31, 2025 include:
Total revenue was $25.9 million, an increase of 73% compared to the fourth quarter of 2024. Wholesale revenue was $15.5 million, or 60% of total revenue, an increase of 213% compared to the fourth quarter of 2024.Online revenue was $10.5 million, or 40% of total revenue, an increase of 4% compared to the fourth quarter of 2024.Excluding the amortization of the inventory step-up related to the Irwin acquisition, gross margin was 37.0% compared to 41.4% during the fourth quarter of 2024, with the decline in gross margin primarily attributable to the acquisition of Irwin, which historically operated at a lower gross margin than Legacy FitLife.Net income was $1.6 million compared to $2.1 million during the fourth quarter of 2024, with the decline driven primarily by transaction expense and amortization of the inventory step-up associated with the acquisition of Irwin.Basic earnings per share and diluted earnings per share were $0.17 and $0.16, respectively, compared to $0.23 and $0.21 during the fourth quarter of 2024.Adjusted EBITDA was $3.5 million, a 14% increase compared to the fourth quarter of 2024.Sales of Irwin products on Amazon scaled from zero at the beginning of the quarter to approximately $0.5 million in the month of December; subsequent to the end of the fourth quarter, Irwin revenue on Amazon has continued to scale to approximately $0.8 million monthly. Highlights for the year ended December 31, 2025 include:
The Company completed the acquisition of Irwin Naturals (“Irwin”) on August 8, 2025Total revenue was $81.5 million, an increase of 26% compared to the prior year.Wholesale revenue was $39.7 million, or 49% of total revenue, an increase of 84% compared to the prior year.Online revenue was $41.8 million, or 51% of total revenue, a decrease of 3% compared to the prior year.Excluding the amortization of the inventory step-up related to the Irwin acquisition, gross margin was 39.9% compared to 43.6% during 2024, with the decline in gross margin primarily attributable to the acquisition of Irwin, which historically operated at a lower gross margin than Legacy FitLifeNet income was $6.3 million compared to $9.0 million during 2024.Basic earnings per share and diluted earnings per share were $0.68 and $0.63, respectively, compared to $0.98 and $0.91 during the prior year.Adjusted EBITDA was $14.0 million compared to $14.1 million in the prior year.The Company ended the year with $39.1 million outstanding on its term loan and $5.6 million outstanding on its revolving line of credit. For the fourth quarter ended December 31, 2025, total revenue was $25.9 million, an increase of 73% compared to $15.0 million during the same period last year. Online revenue for the quarter was $10.5 million, an increase of 4% compared to the quarter ended December 31, 2024. Online revenue accounted for 40% and 67% of the Company’s total revenue during the quarters ended December 31, 2025 and 2024, respectively.
Wholesale revenue for the quarter ended December 31, 2025 was $15.5 million, more than tripling the $4.9 million from the same period last year. The Company’s recent acquisition of Irwin contributed $11.2 million of wholesale revenue for the quarter ended December 31, 2025, while Legacy FitLife wholesale revenue declined $0.7 million, or 14%, compared to the same period last year.
For the year ended December 31, 2025, total revenue was $81.5 million, an increase of 26% compared to $64.5 million in the prior year. Online revenue for the full year was $41.8 million, a 3% decrease compared to $43.0 million in the prior year. Wholesale revenue for the full year was $39.7 million, an increase of 84% compared to $21.5 million in the prior year.
Gross margin for the quarter ended December 31, 2025 was 34.5% compared to 41.4% during the same period in the prior year. Gross margin for the quarter was adversely affected by $0.7 million of amortization of the inventory step-up related to the inventory acquired in the Irwin transaction. Excluding the amortization of the inventory step-up, gross margin for the quarter would have been 37.0%.
Gross margin for the full year ended December 31, 2025 was 38.6% compared to 43.6% during the prior year. Gross margin was adversely affected by $1.0 million of amortization of the inventory step-up related to the inventory acquired in the Irwin transaction. Excluding the amortization of the inventory step-up, gross margin for fiscal 2025 would have been 39.9%
Net income for the fourth quarter of 2025 was $1.6 million compared to $2.1 million during the quarter ended December 31, 2024. Basic and diluted earnings per share were $0.17 and $0.16 respectively, compared to $0.23 and $0.21 during the fourth quarter of 2024.
Net income for the year ended December 31, 2025 was $6.3 million compared to $9.0 million during the prior year. Basic and diluted earnings per share decreased 31% to $0.68 and $0.63 earnings per share, respectively, when compared to the prior year.
Adjusted EBITDA for the quarter ended December 31, 2025 was $3.5 million, an increase of 14% compared to the same period in 2024. Adjusted EBITDA for the year ended December 31, 2025 was $14.0 million, a 1% decrease compared to $14.1 million during the prior year.
As of December 31, 2025, the Company had $39.1 million outstanding on its term loan and $5.6 million outstanding on the revolver, and cash of $1.6 million, or total net debt of approximately $43.1 million.
Performance of Brands
One of the primary metrics used by management to evaluate the performance of the Company’s brands is contribution, a non-GAAP financial measure which management defines as gross profit less advertising and marketing expenditures. Other companies may also report contribution as a performance metric, but their definition or calculation of contribution may differ from the Company’s. Management believes that contribution, as defined by the Company, is a particularly relevant performance metric since it incorporates the gross profit associated with a specific brand or collection of brands as well as the advertising and marketing expenditures associated with the same brand or brands. With limited exceptions, other operating expenses incurred by the Company are generally not allocable to a specific brand or collection of brands.
Legacy FitLife consists of thirteen brands, and Irwin consists of three brands. These collections of brands do not meet the definition of operating segments and are not managed as such.
Legacy FitLife (Unaudited) 2024
2025
Q4 Q1Q2Q3Q4 Wholesale revenue4,939 5,306 5,696 6,686 4,238 Online revenue10,074 10,630 10,431 9,978 9,028 Total revenue15,013 15,936 16,127 16,664 13,266 Gross profit6,212 6,874 6,904 6,542 5,395 Gross margin41.4% 43.1%42.8%39.3%40.7%Advertising and marketing979 1,053 1,191 1,285 1,077 Contribution5,233 5,821 5,713 5,257 4,318 Contribution as a % of revenue34.9% 36.5%35.4%31.5%32.5% For the fourth quarter of 2025, revenue for Legacy FitLife (which now includes MusclePharm as well as MRC) declined 12% compared to the same period last year due to declines in both online and wholesale revenue.
Online revenue decreased by 10% compared to the fourth quarter of 2024, primarily driven by lower online sales from MRC and MusclePharm, partially offset by higher online revenue from the other Legacy FitLife brands. Wholesale revenue decreased 14% as compared to the fourth quarter of 2024.
Gross margin for Legacy FitLife decreased to 40.7% during the fourth quarter of 2025 compared to 41.4% during the fourth quarter of last year. Contribution as a percentage of revenue decreased to 32.5% compared to 34.9% during the fourth quarter of last year.
Irwin (Unaudited) 2025 Q3Q4 Wholesale revenue6,510 11,216 Online revenue311 1,428 Total revenue6,821 12,644 Gross profit2,194 3,544 Gross margin32.2%28.0%Advertising and marketing72 182 Contribution2,122 3,362 Contribution as % of revenue31.1%26.6% The fourth quarter of 2025 is the first full quarter of Irwin’s operating results since the Company acquired Irwin in August 2025. During the quarter, Irwin generated 89% of its revenue from the wholesale channel and 11% from online sales.
Online revenue during the quarter represents transactions through Irwin’s websites as well as through Amazon and other e-commerce platforms. The Company began selling Irwin products on Amazon in mid-October, and sales increased rapidly throughout the quarter to approximately $0.5 million in the month of December.
Normalizing for loss of the customers that occurred prior to the acquisition of Irwin by the Company, as well as for the results of Irwin’s CBD business, which the Company is in the process of exiting, total revenue for Irwin increased approximately 6% in the fourth quarter of 2025 compared to the fourth quarter of 2024.
Irwin generated gross margin of 28.0% and contribution as a percentage of revenue of 26.6% during the fourth quarter of 2025. Excluding amortization of the inventory step-up, Irwin’s gross margin and contribution as a percentage of revenue would have been 33.2% and 31.8%, respectively.
FitLife Consolidated (Unaudited) 2024
2025 Q4 Q1Q2Q3Q4 Wholesale revenue4,939 5,306 5,696 13,196 15,454 Online revenue10,074 10,630 10,431 10,289 10,456 Total revenue15,013 15,936 16,127 23,485 25,910 Gross profit6,212 6,874 6,904 8,736 8,939 Gross margin41.4% 43.1%42.8%37.2%34.5%Advertising and marketing979 1,053 1,191 1,357 1,259 Contribution5,233 5,821 5,713 7,379 7,680 Contribution as % of revenue34.9% 36.5%35.4%31.4%29.6% For the Company overall, revenue for the fourth quarter of 2025 increased 73%, gross profit increased 44%, and contribution increased 47% compared to the fourth quarter of 2024.
Gross margin decreased to 34.5% compared to 41.4% during the fourth quarter of last year, with the decline in gross margin primarily attributable to the acquisition of Irwin, which historically operated at a lower gross margin than Legacy FitLife.
Contribution as a percentage of revenue decreased to 29.6% compared to 34.9% during the fourth quarter of last year. Excluding the impact of the amortization of the inventory step-up at Irwin, gross margin and contribution margin as a percentage of revenue would have been 37.0% and 32.2%, respectively, during the fourth quarter of 2025.
Management commentary
Dayton Judd, the Company’s Chairman and Chief Executive Officer, commented, “Other than at MRC, where revenue declined 15% over the course of the year, 2025 was a strong year for all of our brand groupings. Excluding MRC and MusclePharm, the other Legacy FitLife brands delivered organic growth of 6%. MusclePharm delivered organic growth of 5%, with growth in both the online and wholesale channels. And in its first full quarter of ownership, Irwin delivered organic growth of 6%.
“We began paying down debt during the fourth quarter, with a scheduled amortization payment of $1.5 million on the term loan and an additional $0.4 million reduction on our revolver. During the first quarter, we reduced the outstanding balance on the revolver further by approximately $1.4 million in addition to a scheduled amortization payment on the term loan of $1.5 million on March 31. We intend to continue allocating our available free cash flow to debt reduction.
“During our previous earnings call in November, I provided commentary about emerging weakness we were observing across our brand portfolio. During the first quarter of 2026, this weakness has persisted across most brands and channels. From a macro environment perspective, given the backdrop of economic and political volatility, we know there are broad-based consumer confidence concerns, particularly for discretionary products. Consumer sentiment remains near all-time lows, and consumer discretionary spending has been declining since late last year and is at the lowest level it has been in the past four years. However, we know there are some things we should be doing regardless of the economic environment to improve our performance.
“The Company is focused on five key initiatives that we anticipate will favorably impact revenue and cost in the future. These priorities are to (1) drive meaningful improvement in Irwin’s supply chain, (2) increase focus on new product development at Irwin, (3) drive awareness and demand generation for our products off-Amazon, (4) leverage Irwin’s sales team to cross-sell other FitLife products into the wholesale channel, and (5) reduce SG&A through operating efficiencies.
“Despite the weakness late in the fourth quarter and into the first quarter, I am encouraged by the continued growth of online revenue for Irwin, particularly on Amazon. We ended the fourth quarter at a run rate of approximately $0.5 million of revenue on Amazon from Irwin’s products. I am encouraged that growth has continued throughout the first quarter, with monthly revenue now approximately $0.8 million. In other words, in a few short months, this has become a business with roughly $9-10 million of annual revenue on a run rate basis, with margins higher than our traditional wholesale business. In addition, for a number of reasons, we believe there is the potential for additional long-term revenue and profit growth for Irwin products in this channel. The online growth we are experiencing at Irwin is encouraging, but at this point we are not able to determine whether it will fully or only partially offset the weakness we are experiencing elsewhere in our business.”
Earnings Conference Call
The Company will hold an investor conference call on Wednesday, April 1, 2026 at 4:30 pm ET. Investors interested in participating in the live call can dial (833) 492-0064 from the U.S. and provide the conference identification code of 115536. International participants can dial (973) 528-0163 and provide the same code.
About FitLife Brands
FitLife Brands is a developer and marketer of innovative and proprietary nutritional supplements and wellness products for health-conscious consumers. FitLife markets more than 500 different products online and through various retail locations. FitLife is headquartered in Omaha, Nebraska. For more information, please visit our website at www.fitlifebrands.com.
Forward-Looking Statements
Statements in this release that are forward-looking involve known and unknown risks and uncertainties, which may cause the Company's actual results in future periods to be materially different from any future performance that may be suggested in this news release. Such factors may include, but are not limited to, the ability of the Company to continue to grow revenue, and the Company's ability to continue to achieve positive cash flow given the Company's existing and anticipated operating and other costs. Many of these risks and uncertainties are beyond the Company's control. Reference is made to the discussion of risk factors detailed in the Company's filings with the Securities and Exchange Commission including its reports on Form 10-K and 10-Q. Readers are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the dates on which they are made.
FITLIFE BRANDS, INC.
CONSOLIDATED BALANCE SHEETS
(in thousands, except per share amounts)
December 31, 2025 December 31, 2024 ASSETS: CURRENT ASSETS Cash and cash equivalents $1,646 $4,468 Restricted cash - 52 Accounts receivable, net of allowance for credit losses of $9 and $41, respectively 8,765 1,626 Inventories, net of allowance for obsolescence of $247 and $100, respectively 21,324 11,074 Prepaid expense and other current assets 1,334 923 Total current assets 33,069 18,143 Property and equipment, net 128 75 Right of use asset 682 412 Intangibles, net of amortization of $499 and $152, respectively 51,440 26,235 Goodwill 19,393 13,022 Deferred tax asset 1,525 644 Other assets 83 - TOTAL ASSETS $106,320 $58,531 LIABILITIES AND STOCKHOLDERS' EQUITY: CURRENT LIABILITIES: Accounts payable $6,911 $4,067 Accrued expense 5,429 684 Income taxes payable 1,704 1,415 Product returns 1,039 564 Term loan – current portion 6,094 4,500 Lease liability – current portion 433 81 Total current liabilities 21,610 11,311 Revolving line of credit 5,600 - Term loan, net of current portion and unamortized deferred finance costs 32,849 8,550 Long-term lease liability, net of current portion 272 331 Derivative liability 26 - Deferred tax liability 2,324 2,213 TOTAL LIABILITIES 62,681 22,405 STOCKHOLDERS’ EQUITY: Preferred stock, $0.01 par value, 10,000 shares authorized, none outstanding as of December 31, 2025 and 2024 - - Common stock, $0.01 par value, 120,000 shares authorized; 9,391 and 9,210 issued and outstanding as of December 31, 2025 and 2024 94 92 Additional paid-in capital 32,213 31,129 Retained earnings 11,893 5,567 Accumulated other comprehensive loss (561) (662)TOTAL STOCKHOLDERS' EQUITY 43,639 36,126 TOTAL LIABILITIES AND STOCKHOLDERS' EQUITY $106,320 $58,531 FITLIFE BRANDS, INC.
CONSOLIDATED STATEMENTS OF INCOME
(in thousands, except per share amounts)
Years ended December 31, 2025 2024 Revenue $81,458 $64,469 Cost of goods sold 50,005 36,389 Gross profit 31,453 28,080 OPERATING EXPENSE: Advertising and marketing 4,860 4,626 Selling, general and administrative 14,036 9,972 Merger and acquisition related 2,075 255 Depreciation and amortization 420 108 Total operating expense 21,391 14,961 OPERATING INCOME 10,062 13,119 OTHER EXPENSE (INCOME) Interest income (98) (69)Interest expense 1,863 1,367 Other expense 49 - Foreign exchange loss (gain) 19 (50)Total other expense, net 1,833 1,248 INCOME BEFORE INCOME TAX PROVISION 8,229 11,871 PROVISION FOR INCOME TAXES 1,903 2,887 NET INCOME $6,326 $8,984 NET INCOME PER SHARE Basic $0.68 $0.98 Diluted $0.63 $0.91 Basic weighted average common shares 9,347 9,197 Diluted weighted average common shares 9,977 9,898 FITLIFE BRANDS, INC.
CONSOLIDATED STATEMENTS OF CASH FLOWS
(in thousands)
Years ended December 31, 2025 2024 CASH FLOWS FROM OPERATING ACTIVITIES: Net income $6,326 $8,984 Adjustments to reconcile net income to net cash provided by operating activities: Depreciation and amortization 420 108 Allowance for credit losses (32) 24 Allowance for inventory obsolescence 147 (62)Stock-based compensation 404 459 Amortization of deferred finance costs 40 41 Write-off of deferred financing costs 49 - Amortization of inventory step-up 1,045 - Changes in operating assets and liabilities: Accounts receivable - trade 210 361 Inventories (582) (2,109)Deferred taxes (881) 148 Prepaid expense and other assets 200 692 Right of use asset 242 90 Accounts payable 743 866 Income taxes payable (54) 634 Lease liability (223) (107)Accrued liabilities and other liabilities (582) (512)Product returns (33) (7)Net cash provided by operating activities 7,439 9,610 CASH FLOWS FROM INVESTING ACTIVITIES: Cash paid for Irwin acquisition (42,500) - Purchase of property and equipment (42) (10)Net cash used in investing activities (42,542) (10) CASH FLOWS FROM FINANCING ACTIVITIES: Proceeds from exercise of stock options 682 17 Borrowings on 2025 term loan 40,452 - Payments on 2025 term loan (1,523) - Payoff of 2023 term loans (10,875) - Payments on 2023 term loans (2,250) (7,000)Borrowings on line of credit 5,600 - Net cash provided by (used in) financing activities 32,086 (6,983) Foreign currency impact on cash 143 5 CHANGE IN CASH AND RESTRICTED CASH (2,874) 2,622 CASH AND RESTRICTED CASH, BEGINNING OF PERIOD 4,520 1,898 CASH AND CASH EQUIVALENTS, END OF PERIOD $1,646 $4,520 Supplemental cash flow disclosure Cash paid for income taxes $2,362 $2,498 Cash paid for interest, net of amounts capitalized $1,748 $1,361 Non-cash investing and financing activities Addition to right-of-use assets from new operating lease liabilities $- $386 Non-GAAP Financial Measures
The financial information included in this release and the presentation below contain certain financial measures defined as “non-GAAP financial measures” by the SEC, including non-GAAP EBITDA and non-GAAP adjusted EBITDA. These measures may be different from non-GAAP financial measures used by other companies. The presentation of this financial information, which is not prepared under any comprehensive set of accounting rules or principles, is not intended to be considered in isolation or as a substitute for the financial information prepared and presented in accordance with GAAP.
As presented below, non-GAAP EBITDA excludes interest, foreign currency gain/loss, income taxes, and depreciation and amortization. Adjusted non-GAAP EBITDA excludes, in addition to interest, foreign currency gain/loss, taxes, depreciation and amortization, equity-based compensation, M&A/integration expense, restructuring and non-recurring gains or losses. The Company believes the non-GAAP measures provide useful information to both management and investors by excluding certain expense and other items that may not be indicative of its core operating results and business outlook. The Company believes that the inclusion of non-GAAP measures in the financial presentation below allows investors to compare the Company’s financial results with the Company’s historical financial results and is an important measure of the Company’s comparative financial performance.
The Company’s calculation of Adjusted EBITDA for the year ended December 31, 2025 and 2024 is as follows:
Year ended December 31, 2025 2024 (Unaudited) (Unaudited) Net income $6,326 $8,984 Interest expense 1,863 1,367 Interest income (98) (69)Foreign exchange (gain) loss 19 (50)Provision for income taxes 1,903 2,887 Depreciation and amortization 420 108 EBITDA 10,433 13,227 Non-cash and non-recurring adjustments Stock-based compensation 404 459 Merger and acquisition related 2,075 255 Amortization of inventory step-up 1,045 - Writeoff of deferred financing costs 49 - Restructuring costs - 184 Adjusted EBITDA $14,006 $14,125
FitLife Brands (NASDAQ:FTLF) executives said the company’s fourth quarter and full-year fiscal 2025 results were shaped by the August 2025 acquisition of Irwin Naturals, while also acknowledging broad-based demand softness that intensified late in the fourth quarter and has persisted into the first quarter of 2026.
CEO Dayton Judd said the fourth quarter was the first full quarter to include Irwin Naturals’ financial results. CFO Jakob York joined the call; EVP Ryan Hansen was on vacation.
Full-year 2025: Growth in most brand groupings, except MRC Judd said 2025 was “a strong year for all of our brand groupings other than MRC.” He reported that Legacy FitLife (excluding MRC and MusclePharm) delivered approximately 6% organic revenue growth, with wholesale revenue flat and online revenue up about 16% for the year. MusclePharm delivered about 5% organic revenue growth in 2025, with growth in both wholesale and online channels, while MRC revenue declined approximately 15%.
Judd also provided historical context for Irwin Naturals, noting that the brand’s results prior to FitLife’s ownership were affected by several factors that no longer reflect the go-forward business, including the discontinuation of the final Irwin product at Costco U.S. in early 2025, Rite Aid’s bankruptcy and liquidation, and FitLife’s post-acquisition decision to exit CBD.
Judd said Irwin historically generated meaningful CBD revenue, totaling about $4.8 million in gross revenue in the 12 months prior to the acquisition, but FitLife decided to discontinue all CBD products after the deal. The company expects to be fully out of CBD inventory “later in 2026,” he said.
After adjusting for Costco U.S., Rite Aid, and CBD, Judd said Irwin’s net revenue would have been $54 million for full-year 2024 and $54 million for full-year 2025—flat year over year on a normalized basis.
Fourth quarter results: Revenue jumps on Irwin acquisition, margins pressured For the fourth quarter of 2025, FitLife reported total revenue of $25.9 million, up 73% year over year, “primarily as a result of the acquisition of Irwin,” Judd said, partially offset by weakness in Legacy FitLife. Wholesale revenue rose to $15.5 million, or 60% of revenue, up 213%, while online revenue was $10.5 million, or 40% of revenue, up 4%.
Excluding amortization of the inventory step-up related to the Irwin acquisition, gross margin was 37.0%, down from 41.4% a year earlier. Judd attributed the decline primarily to Irwin’s historically lower margin profile, while adding that management expects improvement over time. Contribution (gross profit less advertising and marketing expense) increased 47%, driven mainly by Irwin, but was partially offset by lower contribution from Legacy FitLife.
Net income was $1.6 million, down from $2.1 million in the year-ago quarter, which Judd said was driven primarily by transaction-related expenses and the inventory step-up amortization. Adjusted EBITDA was $3.5 million, up 14% year over year.
During Q&A, Judd said the inventory step-up amortization ended in the fourth quarter: “In the Q1 numbers and beyond, you will not see any amortization of inventory step-up.”
Brand performance: Legacy FitLife softness; Irwin shows early Amazon momentum Judd said the company began seeing “broad-based weakness across our portfolio of brands” around mid-November, and that weakness accelerated late in the fourth quarter and into the first quarter. He pointed to consumer confidence concerns and weaker discretionary spending, adding that consumer sentiment “remains near all-time lows.”
Total Legacy FitLife revenue in the fourth quarter was $13.3 million, with 68% from online sales and 32% from wholesale customers. Judd said wholesale revenue declined 14% year over year and online revenue fell 10%, for a total decline of 12%. The declines were primarily attributable to MRC and MusclePharm; excluding those two, the other Legacy FitLife brands delivered 4% organic growth in the quarter, he said.
Legacy FitLife gross margin declined to 40.7% from 41.4%, and contribution fell 18% to $4.3 million. Excluding MRC and MusclePharm, Judd said the remaining brands delivered higher revenue, higher gross margin, and higher contribution as a percentage of revenue compared with the prior-year quarter.
Irwin produced $12.6 million of revenue in the quarter, with $11.2 million (89%) from wholesale and 11% from online. Reported gross margin was 28.0% and contribution margin was 26.6%. Adjusting for the inventory step-up amortization, Judd said Irwin gross margin would have been 33.2% and contribution margin would have been 31.8%.
Judd highlighted accelerating momentum on Amazon after FitLife began selling Irwin products there in mid-October. He said Amazon revenue for Irwin scaled from about $60,000 in October to $300,000 in November and nearly $500,000 in December. He added that growth continued into the first quarter of 2026, with Irwin’s monthly Amazon revenue now approximately $0.8 million, implying a $9 million to $10 million annualized run rate.
Judd also said Irwin’s subscriber growth has been strong, with subscribers increasing from about 500 at the beginning of 2026 to over 3,600 “today,” contrasting that with declines in subscriber counts across most other brands. He attributed the broader subscriber declines to an Amazon change made around late September that switched the default buy box from Subscribe & Save to one-time purchase.
Balance sheet and 2026 priorities: Supply chain fixes, marketing shift, and no guidance On the balance sheet, Judd said FitLife began scheduled amortization on its term loan in the fourth quarter and paid down about $1.9 million of debt during the quarter, ending with a $44.7 million debt balance. He added that the company reduced its revolver balance by $1.4 million during the first quarter and made another scheduled term-loan amortization payment of about $1.5 million “yesterday,” saying FitLife is “ahead of schedule” on debt reduction and intends to continue using excess free cash flow to pay down debt.
Judd said management has identified five priorities to address weak performance and improve revenue and costs over time:
Improve Irwin’s supply chain, including reducing roughly $2 million of annual obsolete inventory disposal. Judd said moving products from two-year to three-year dating could potentially lift Irwin gross margin by 300 to 400 basis points, with a “dollar-for-dollar impact on EBITDA.” FitLife hired a new VP of operations for Irwin in February and expects meaningful supply chain improvements through 2026. Increase Irwin new product development, with three new products currently in production that FitLife expects to launch in the third quarter. Drive off-Amazon awareness and demand generation, as Judd said FitLife believes Amazon’s evolving algorithms increasingly reward listings that bring external traffic. He cited Irwin as the fastest-growing FitLife Amazon account and described efforts to build off-Amazon presence for Dr. Tobias, including TikTok brand ambassadors and a partnership with competitive eater Joey Chestnut tied to Dr. Tobias’s Hero Colon Cleanse product. Cross-sell into wholesale using Irwin’s sales team, noting FitLife recently gained placement of six MusclePharm SKUs in a regional grocery chain beginning in the second quarter, with additional retailer conversations underway. Continue SG&A efficiency efforts, including exiting MRC’s Toronto-area office lease and expecting Irwin’s lease renewal later in the year to be for a smaller space at a lower cost per square foot. Asked about the relative impact of macro pressure versus Amazon-specific headwinds, Judd said he could not confidently bifurcate the two. He noted that point-of-sale data shows supplement category growth has been declining for about six months and recently turned negative, but he also pointed to additional variables such as out-of-stocks that are “hard to quantify.”
On gross margin expectations, Judd said returning to 40% may be difficult given Irwin’s historical margin profile, but he expects improvement. He told one analyst that a consolidated gross margin “closer to high 30s% is reasonable” over time as supply chain issues are addressed.
FitLife declined to provide formal guidance for 2026. Judd said the company is holding off due to continued weakness in the first quarter and uncertainty about how long exogenous challenges will persist and how quickly internal initiatives will translate into results. He told investors that “Q1 looks a whole lot like Q4,” indicating the company is not seeing a typical seasonal lift so far.
Judd also addressed questions about MusclePharm, noting the brand continues to face elevated protein input costs and broader protein category dynamics. He said FitLife declined a roughly $1.5 million purchase order from an international customer in the first quarter due to what would have been the lowest gross margin the company had ever sold at, emphasizing the company’s intent to protect profitability rather than chase revenue.
On Irwin and Costco U.S., Judd said FitLife has held discussions but does not expect to regain Costco U.S. distribution “anytime soon.” He noted Irwin continues to sell in Costco Canada and said there have been no SKU losses there since FitLife acquired the business.
About FitLife Brands (NASDAQ:FTLF) FitLife Brands, Inc provides nutritional supplements for health-conscious consumers in the United States and internationally. The company provides weight loss, sports nutrition, and general health products; sports nutrition products; weight loss and sports nutrition products; sports nutrition and general wellness formulations with an emphasis on natural, vegan, and organic ingredients; and male health and weight loss products, as well as other diet, health, and sports nutrition supplements and related products; and value-oriented sports nutrition and weight loss products.
Read More Five stocks we like better than FitLife Brands
Key Takeaways FitLife Brands saw the consumer slow wellness purchases to start the year. Earnings estimates have been slashed on FTLF for 2026 and 2027. Shares of FitLife Brands are at 52-week lows but are cheap, with a forward P/E of 10.8. FitLife Brands, Inc. (FTLF - Free Report) is seeing a slowdown in consumer spending on nutritional supplements and wellness products. This Zacks Rank #5 (Strong Sell) is expected to see earnings decline in 2026.
FitLife Brands develops proprietary nutritional supplements and wellness products for health-conscious consumers. It markets more than 500 different products online and through various retail locations.
Some of its brands include Dr. Tobias, PMD, Siren Labs, MusclePharm, and Maritime Naturals.
FitLife Brands Sees Big Growth for Irwin on AmazonOn Aug 8, 2025, FitLife Brands acquired Irwin Naturals. It put Irwin products on Amazon in Oct 2025, where it began at zero sales. It scaled to approximately $0.5 million in the month of December.
Subsequent to the end of the fourth quarter 2025, Irwin revenue on Amazon continued to scale to approximately $0.8 million monthly. This was also at margins higher than their traditional wholesale business.
A key initiative for 2026 is to leverage Irwin’s sales team to cross-sell Irwin’s other brands across the wholesale channel.
Consumer Slows Down in 2026FitLife Brands reported fourth quarter 2025 results on Apr 1, 2026, so it already had seen the results of the first few months of the new year.
“During our previous earnings call in November, I provided commentary about emerging weakness we were observing across our brand portfolio. During the first quarter of 2026, this weakness has persisted across most brands and channels,” said Dayton Judd, Chairman and CEO.
“From a macro environment perspective, given the backdrop of economic and political volatility, we know there are broad-based consumer confidence concerns, particularly for discretionary products,” he added.
Earnings Estimates are Slashed for 2026 and 2027It shouldn’t be a surprise, given the company’s gloomy outlook on the consumer, that the earnings estimates have been cut.
FitLife is a small cap company with a market cap of just $87.5 million. Zacks only has estimates from one analyst.
That analyst cut the 2026 and 2027 earnings estimate in the last 30 days. For 2026, it fell to $0.86 from $1.62. That’s an earnings decline of 8.5% as FitLife made $0.94 in 2025.
The 2027 earnings consensus also fell to $1.19 from $1.82 in the prior month. But that’s an earnings gain of 38.4%.
However, both of these were big cuts to the estimates. Here’s what it looks like on the price and consensus chart.
Image Source: Zacks Investment Research
Shares of FitLife Slide in 2026Given all the uncertainty about the consumer this year, it’s not a surprise that the shares have slid in 2026. They’re at 52-week lows.
Image Source: Zacks Investment Research
But FitLife is now cheap. It trades with a forward price-to-earnings (P/E) ratio of 10.8. A P/E under 15 usually means a company has value.
It also has other attractive valuations like a price-to-book (P/B) ratio of just 2. A P/B ratio of 3.0 and under usually means a company is undervalued.
As of Dec 31, 2025, FitLife had $39.1 million outstanding on its term loan and $5.6 million outstanding on the revolver. FitLife’s cash was $1.6 million, giving it a total net debt of $43.1 million.
For investors looking to invest in a wellness company, it might be best to stay on the sidelines with FitLife Brands until the consumer starts buying again.
OMAHA, NE, May 05, 2026 (GLOBE NEWSWIRE) -- FitLife Brands, Inc. (“FitLife,” or the “Company”) (Nasdaq: FTLF), a provider of innovative and proprietary nutritional supplements and wellness products, today announced that it plans to report its financial performance for the first quarter of fiscal 2026 on Thursday, May 14, 2026.
In addition, the Company announced that it will hold an investor conference call after market close on May 14, 2026 at 5:00 pm ET. Investors interested in participating in the live call can dial (833) 492-0064 from the U.S. and provide the conference identification code of 133048. International participants can dial (973) 528-0163 and provide the same code.
About FitLife Brands
FitLife Brands is a developer and marketer of innovative and proprietary nutritional supplements and wellness products for health-conscious consumers. FitLife markets over 500 different products online and through various retail locations. FitLife is headquartered in Omaha, Nebraska. For more information, please visit our website at www.fitlifebrands.com.
OMAHA, NE, May 14, 2026 (GLOBE NEWSWIRE) -- FitLife Brands, Inc. (“FitLife” or the “Company”) (NASDAQ: FTLF), a provider of innovative and proprietary nutritional supplements and wellness products, today announced financial results for the first quarter ended March 31, 2026.
Highlights for the first quarter ended March 31, 2026 include:
Total revenue was $25.3 million, an increase of 59% compared to the first quarter of 2025. Wholesale revenue was $14.1 million, or 56% of total revenue, an increase of 166% compared to the first quarter of 2025.Online revenue was $11.2 million, or 44% of total revenue, an increase of 6% compared to the first quarter of 2025.Gross margin was 37.6% compared to 43.1% during the first quarter of 2025, with the decline in gross margin primarily attributable to the acquisition of Irwin, which historically operated at a lower gross margin than Legacy FitLife.Net income was $1.7 million compared to $2.0 million during the first quarter of 2025, with the decline driven by higher amortization expense and interest expense associated with the acquisition of Irwin.Basic earnings per share and diluted earnings per share were $0.18 and $0.17, respectively, compared to $0.22 and $0.20 during the first quarter of 2025.Adjusted EBITDA was $3.3 million, a 3% decrease compared to the first quarter of 2025.The Company ended the quarter with $37.6 million outstanding on its term loan and $4.2 million outstanding on its revolving line of credit. For the first quarter ended March 31, 2026, total revenue was $25.3 million, an increase of 59% compared to $15.9 million during the same period last year.
Wholesale revenue for the quarter ended March 31, 2026 was $14.1 million, a 166% increase from the same period last year. The Company’s recent acquisition of Irwin contributed $10.3 million of wholesale revenue for the quarter ended March 31, 2026, while Legacy FitLife wholesale revenue declined $1.5 million, or 28%, compared to the same period last year.
Online revenue for the quarter was $11.2 million, an increase of 6% compared to the quarter ended March 31, 2025. Online revenue accounted for 44% and 67% of the Company’s total revenue during the quarters ended March 31, 2026 and 2025, respectively.
Gross margin for the quarter ended March 31, 2026 was 37.6% compared to 43.1% during the same period in the prior year. The decrease in gross margin is primarily attributable to the acquisition of Irwin, which historically generated a lower gross margin than Legacy FitLife.
Net income for the first quarter of 2026 was $1.7 million compared to $2.0 million during the quarter ended March 31, 2025. Basic and diluted earnings per share for the first quarter of 2026 were $0.18 and $0.17, respectively, compared to $0.22 and $0.20 during the first quarter of 2025.
Adjusted EBITDA for the quarter ended March 31, 2026 was $3.3 million, a decrease of 3% compared to the same period in 2025.
As of March 31, 2026, the Company had $37.6 million outstanding on its term loan and $4.2 million outstanding on the revolver, and cash of $1.2 million, or total net debt of approximately $40.6 million, compared to $43.1 million as of December 31, 2025.
Performance of Brands
One of the primary metrics used by management to evaluate the performance of the Company’s brands is contribution, a non-GAAP financial measure which management defines as gross profit less advertising and marketing expenditures. Other companies may also report contribution as a performance metric, but their definition or calculation of contribution may differ from the Company’s. Management believes that contribution, as defined by the Company, is a particularly relevant performance metric since it incorporates the gross profit associated with a specific brand or collection of brands as well as the advertising and marketing expenditures associated with the same brand or brands. With limited exceptions, other operating expenses incurred by the Company are generally not allocable to a specific brand or collection of brands.
Legacy FitLife consists of thirteen brands, and Irwin consists of three brands. These collections of brands do not meet the definition of operating segments and are not managed as such.
Legacy FitLife (Unaudited) 2025 2026 Q1Q2Q3Q4 Q1 Wholesale revenue5,306 5,696 6,686 4,238 3,798 Online revenue10,630 10,431 9,978 9,028 8,678 Total revenue15,936 16,127 16,664 13,266 12,476 Gross profit6,874 6,904 6,542 5,395 5,143 Gross margin43.1%42.8%39.3%40.7% 41.2%Advertising and marketing1,053 1,191 1,285 1,077 887 Contribution5,821 5,713 5,257 4,318 4,256 Contribution as % of revenue36.5%35.4%31.5%32.5% 34.1% For the first quarter of 2026, revenue for Legacy FitLife declined 22% compared to the same period last year due to declines in both online and wholesale revenue. Wholesale revenue decreased 28% as compared to the first quarter of 2025 due to lower sales to certain retail partners, primarily GNC. Online revenue decreased by 18% compared to the first quarter of 2025, primarily driven by lower online sales from MRC.
Gross margin for Legacy FitLife decreased to 41.2% during the first quarter of 2026 compared to 43.1% during the first quarter of last year. Contribution as a percentage of revenue decreased to 34.1% compared to 36.5% during the first quarter of last year.
Irwin (Unaudited) 2025
2026
Q3Q4 Q1 Wholesale revenue6,510 11,216 10,295 Online revenue311 1,428 2,554 Total revenue6,821 12,644 12,849 Gross profit2,194 3,544 4,374 Gross margin32.2%28.0% 34.0%Advertising and marketing72 182 358 Contribution2,122 3,362 4,016 Contribution as % of revenue31.1%26.6% 31.3% During the first quarter of 2026, Irwin generated 80% of its revenue from the wholesale channel and 20% from online sales. Total revenue for Irwin for the first quarter of 2026 increased 2% sequentially from the fourth quarter of 2025.
Normalizing for loss of the customers that occurred prior to the acquisition of Irwin by the Company, as well as for the results of Irwin’s CBD business, which the Company is in the process of exiting, total revenue for Irwin decreased approximately 13% in the first quarter of 2026 compared to the first quarter of 2025. Management believes that the year-over-year revenue decline for Irwin is primarily a function of a weak consumer environment, a lack of new product launches, and supply chain challenges including inventory out-of-stock situations.
Online revenue during the quarter represents transactions through Irwin’s websites as well as through Amazon and other e-commerce platforms. The Company began selling Irwin products on Amazon in mid-October, and sales increased rapidly throughout the quarter, with a sequential increase in online revenue of 79% compared to the fourth quarter of 2025. At the end of the first quarter of 2026, Irwin’s Amazon sales reached a run-rate of approximately $9.6 million in annual revenue.
Irwin generated gross margin of 34.0% and contribution as a percentage of revenue of 31.3% during the first quarter of 2026. Excluding amortization of the inventory step-up during the fourth quarter of 2025, Irwin’s gross margin and contribution as a percentage of revenue would have been 33.2% and 31.8%, respectively.
FitLife Consolidated (Unaudited) 2025
2026
Q1Q2Q3Q4 Q1 Wholesale revenue5,306 5,696 13,196 15,454 14,093 Online revenue10,630 10,431 10,289 10,456 11,232 Total revenue15,936 16,127 23,485 25,910 25,325 Gross profit6,874 6,904 8,736 8,939 9,517 Gross margin43.1%42.8%37.2%34.5% 37.6%Advertising and marketing1,053 1,191 1,357 1,259 1,245 Contribution5,821 5,713 7,379 7,680 8,272 Contribution as % of revenue36.5%35.4%31.4%29.6% 32.7% For the Company overall, revenue for the first quarter of 2026 increased 59%, gross profit increased 38%, and contribution increased 42% compared to the first quarter of 2025.
Gross margin decreased to 37.6% compared to 43.1% during the first quarter of last year, with the decline in gross margin primarily attributable to the acquisition of Irwin, which historically operated at a lower gross margin than Legacy FitLife.
Contribution as a percentage of revenue decreased to 32.7% compared to 36.5% during the first quarter of last year.
Management commentary
Dayton Judd, the Company’s Chairman and Chief Executive Officer, commented, “As previously disclosed, the first quarter of 2026 was a challenging one. The consumer weakness that we initially observed early in the fourth quarter of 2025 accelerated late in the fourth quarter and into the first quarter of 2026. In addition, apparent changes in the Amazon algorithms are causing the Company to alter how it promotes its products.
“In addition to those exogenous challenges, supply chain difficulties at Irwin also negatively impacted revenue as we dealt with a number of out-of-stock situations for some of our high-velocity products. We estimate that out-of-stock situations resulted in lost revenue of $1.0-1.5 million for Irwin during the first quarter, or more than half of the year-over-year organic decline experienced in the first quarter of 2026.
“As has been our practice, we continue to allocate our available free cash flow to debt reduction. During the first quarter, we made a scheduled amortization payment of $1.5 million on our term loan in addition to a $1.4 million paydown on our revolving line of credit.
“While the macro environment and other variables remain challenging, I am encouraged by some signs of improvement in our business. More specifically, monthly revenue increased sequentially throughout the first quarter. In addition, most of our Amazon selling accounts showed sequential improvement over the course of the quarter. Also, we are pleased to announce the launch of two MusclePharm SKUs in several hundred Kroger stores nationwide beginning in June.
“Last, we remain excited about the growth of Irwin on Amazon. As previously disclosed, monthly revenue for Irwin on Amazon increased from approximately $0.5 million in December of 2025 to approximately $0.8 million in March of 2026. In the month of April, Irwin revenue on Amazon was approximately $0.9 million. Although the growth rate is slowing due to the higher base of sales, we have experienced further sequential growth in the May month-to-date period. Going forward, we expect continued future growth on Amazon for Irwin as we (1) continue to resolve the out-of-stock situations, (2) successfully set up listings for our remaining products that have not yet been available for sale on Amazon, and (3) launch our portfolio of Canadian products on Amazon Canada later in the second quarter.”
Earnings Conference Call
The Company will hold an investor conference call on Thursday, May 14, 2026 at 5:00 pm ET. Investors interested in participating in the live call can dial (833) 492-0064 from the U.S. and provide the conference identification code of 133048. International participants can dial (973) 528-0163 and provide the same code.
About FitLife Brands
FitLife Brands is a developer and marketer of innovative and proprietary nutritional supplements and wellness products for health-conscious consumers. FitLife markets more than 500 different products online and through various retail locations. FitLife is headquartered in Omaha, Nebraska. For more information, please visit our website at www.fitlifebrands.com.
Forward-Looking Statements
Statements in this release that are forward-looking involve known and unknown risks and uncertainties, which may cause the Company's actual results in future periods to be materially different from any future performance that may be suggested in this news release. Such factors may include, but are not limited to, the ability of the Company to continue to grow revenue, and the Company's ability to continue to achieve positive cash flow given the Company's existing and anticipated operating and other costs. Many of these risks and uncertainties are beyond the Company's control. Reference is made to the discussion of risk factors detailed in the Company's filings with the Securities and Exchange Commission including its reports on Form 10-K and 10-Q. Readers are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the dates on which they are made.
FITLIFE BRANDS, INC.
CONDENSED CONSOLIDATED BALANCE SHEETS
(in thousands, except per share amounts)
March 31, 2026 December 31, 2025 (Unaudited) ASSETS: CURRENT ASSETS Cash and cash equivalents $1,192 $1,646 Accounts receivable, net 7,778 8,765 Inventories, net 21,528 21,324 Prepaid expense and other current assets 1,142 1,334 Total current assets 31,640 33,069 Property and equipment, net 106 128 Right of use asset 581 682 Intangibles, net 51,196 51,440 Goodwill 19,363 19,393 Deferred tax asset 1,222 1,525 Derivative asset 72 - Other assets 89 83 TOTAL ASSETS $104,269 $106,320 LIABILITIES AND STOCKHOLDERS' EQUITY: CURRENT LIABILITIES: Accounts payable $6,451 $6,911 Accrued expense 5,602 5,429 Income taxes payable 1,494 1,704 Product returns 830 1,039 Term loan – current portion 6,094 6,094 Lease liability – current portion 341 433 Total current liabilities 20,812 21,610 Revolving line of credit 4,200 5,600 Term loan, net of current portion and unamortized deferred finance costs 31,334 32,849 Long-term lease liability, net of current portion 258 272 Derivative liability - 26 Deferred tax liability 2,284 2,324 TOTAL LIABILITIES 58,888 62,681 STOCKHOLDERS’ EQUITY: Preferred stock, $0.01 par value, 10,000 shares authorized, none outstanding as of March 31, 2026 and December 31, 2025 - - Common stock, $0.01 par value, 120,000 shares authorized; 9,391 issued and outstanding as of March 31, 2026 and December 31, 2025 94 94 Additional paid-in capital 32,230 32,213 Retained earnings 13,613 11,893 Accumulated other comprehensive loss (556) (561)TOTAL STOCKHOLDERS' EQUITY 45,381 43,639 TOTAL LIABILITIES AND STOCKHOLDERS' EQUITY $104,269 $106,320 FITLIFE BRANDS, INC.
CONDENSED CONSOLIDATED STATEMENTS OF INCOME
(in thousands, except per share data)
(Unaudited)
Three months ended March 31, 2026
2025 Revenue $25,325 $15,936 Cost of goods sold 15,808 9,062 Gross profit 9,517 6,874 OPERATING EXPENSE: Advertising and marketing 1,245 1,053 Selling, general and administrative 4,963 2,512 Merger and acquisition related - 332 Depreciation and amortization 248 19 Total operating expense 6,456 3,916 OPERATING INCOME 3,061 2,958 OTHER EXPENSE Interest expense, net 735 218 Foreign exchange (gain) loss (21) 21 Total other expense, net 714 239 INCOME BEFORE INCOME TAX PROVISION 2,347 2,719 PROVISION FOR INCOME TAXES 627 701 NET INCOME $1,720 $2,018 NET INCOME PER SHARE Basic $0.18 $0.22 Diluted $0.17 $0.20 Basic weighted average common shares 9,391 9,213 Diluted weighted average common shares 9,991 9,926 FITLIFE BRANDS, INC.
CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS (in thousands)
Three months ended March 31, 2026 2025 CASH FLOWS FROM OPERATING ACTIVITIES: Net income $1,720 $2,018 Adjustments to reconcile net income to net cash provided by operating activities: Depreciation and amortization 248 19 Allowance for credit losses 58 (3)Allowance for inventory obsolescence (105) (24)Stock-based compensation 17 107 Amortization of deferred financing costs 9 11 Changes in operating assets and liabilities: Accounts receivable 921 (1,062)Inventories 16 (1,013)Deferred taxes 303 (47)Prepaid expense and other assets 94 362 Right of use asset 101 27 Accounts payable (452) 1,168 Income taxes payable (185) 318 Lease liability (105) (20)Accrued expense and other liabilities 53 449 Product returns (209) 18 Net cash provided by operating activities 2,484 2,328 CASH FLOWS FROM INVESTING ACTIVITIES: Purchase of property and equipment - (24)Net cash used in investing activities - (24) CASH FLOWS FROM FINANCING ACTIVITIES: Proceeds from exercise of stock options - 259 Payments on 2025 term loan (1,524) - Payments on 2023 term loan - (1,125)Payments on line of credit (1,400) - Net cash used in financing activities (2,924) (866) Foreign currency impact on cash (14) 36 CHANGE IN CASH AND CASH EQUIVALENTS (454) 1,474 CASH AND CASH EQUIVALENTS, BEGINNING OF PERIOD 1,646 4,520 CASH AND CASH EQUIVALENTS, END OF PERIOD $1,192 $5,994 Supplemental cash flow disclosure Cash paid for income taxes $430 $408 Cash paid for interest $742 $238 Non-GAAP Financial Measures
The financial information included in this release and the presentation below contain certain financial measures defined as “non-GAAP financial measures” by the SEC, including non-GAAP EBITDA and non-GAAP adjusted EBITDA. These measures may be different from non-GAAP financial measures used by other companies. The presentation of this financial information, which is not prepared under any comprehensive set of accounting rules or principles, is not intended to be considered in isolation or as a substitute for the financial information prepared and presented in accordance with GAAP.
As presented below, non-GAAP EBITDA excludes interest, foreign exchange gains and losses, income taxes, and depreciation and amortization. Adjusted non-GAAP EBITDA excludes, in addition to interest, foreign exchange gains and losses, income taxes, depreciation and amortization, stock-based compensation and merger and acquisition related expense and non-recurring gains or losses. The Company believes the non-GAAP measures provide useful information to both management and investors by excluding certain expense and other items that may not be indicative of its core operating results and business outlook. The Company believes that the inclusion of non-GAAP measures in the financial presentation below allows investors to compare the Company’s financial results with the Company’s historical financial results and is an important measure of the Company’s comparative financial performance.
The Company’s calculation of Adjusted EBITDA for the three months ended March 31, 2026 and 2025 is as follows:
Three months ended March 31, 2026 2025 (Unaudited) (Unaudited) Net income $1,720 $2,018 Interest expense, net 735 218 Foreign exchange (gain) loss (21) 21 Provision for income taxes 627 701 Depreciation and amortization 248 19 EBITDA 3,309 2,977 Non-cash and non-recurring adjustments Stock-based compensation 17 107 Merger and acquisition related - 332 Adjusted EBITDA $3,326 $3,416
FitLife Brands Inc. (FTLF - Free Report) came out with quarterly earnings of $0.17 per share, beating the Zacks Consensus Estimate of $0.14 per share. This compares to earnings of $0.2 per share a year ago. These figures are adjusted for non-recurring items.
This quarterly report represents an earnings surprise of +21.43%. A quarter ago, it was expected that this company would post earnings of $0.25 per share when it actually produced earnings of $0.25, delivering no surprise.
Over the last four quarters, the company has surpassed consensus EPS estimates just once.
FitLife Brands , which belongs to the Zacks Medical - Products industry, posted revenues of $25.33 million for the quarter ended March 2026, missing the Zacks Consensus Estimate by 1.61%. This compares to year-ago revenues of $15.94 million. The company has not been able to beat consensus revenue estimates over the last four quarters.
The sustainability of the stock's immediate price movement based on the recently-released numbers and future earnings expectations will mostly depend on management's commentary on the earnings call.
FitLife Brands shares have lost about 41.4% since the beginning of the year versus the S&P 500's gain of 8.8%.
What's Next for FitLife Brands ?While FitLife Brands has underperformed the market so far this year, the question that comes to investors' minds is: what's next for the stock?
There are no easy answers to this key question, but one reliable measure that can help investors address this is the company's earnings outlook. Not only does this include current consensus earnings expectations for the coming quarter(s), but also how these expectations have changed lately.
Empirical research shows a strong correlation between near-term stock movements and trends in earnings estimate revisions. Investors can track such revisions by themselves or rely on a tried-and-tested rating tool like the Zacks Rank, which has an impressive track record of harnessing the power of earnings estimate revisions.
Ahead of this earnings release, the estimate revisions trend for FitLife Brands was unfavorable. While the magnitude and direction of estimate revisions could change following the company's just-released earnings report, the current status translates into a Zacks Rank #5 (Strong Sell) for the stock. So, the shares are expected to underperform the market in the near future. You can see the complete list of today's Zacks #1 Rank (Strong Buy) stocks here.
It will be interesting to see how estimates for the coming quarters and the current fiscal year change in the days ahead. The current consensus EPS estimate is $0.20 on $27.14 million in revenues for the coming quarter and $0.86 on $110.74 million in revenues for the current fiscal year.
Investors should be mindful of the fact that the outlook for the industry can have a material impact on the performance of the stock as well. In terms of the Zacks Industry Rank, Medical - Products is currently in the bottom 35% of the 250 plus Zacks industries. Our research shows that the top 50% of the Zacks-ranked industries outperform the bottom 50% by a factor of more than 2 to 1.
Medtronic (MDT - Free Report) , another stock in the same industry, has yet to report results for the quarter ended April 2026. The results are expected to be released on June 3.
This medical device company is expected to post quarterly earnings of $1.58 per share in its upcoming report, which represents a year-over-year change of -2.5%. The consensus EPS estimate for the quarter has remained unchanged over the last 30 days.
Medtronic's revenues are expected to be $9.66 billion, up 8.2% from the year-ago quarter.
FitLife Brands NASDAQ: FTLF reported sharply higher first-quarter 2026 revenue, driven by the acquisition of Irwin, while profitability declined as the company absorbed lower Irwin margins and higher acquisition-related expenses.
Chief Executive Officer Dayton Judd said total revenue for the quarter was $25.3 million, up 59% from the same period last year. Wholesale revenue was $14.1 million, or 56% of total revenue, increasing 166% year over year. Online revenue was $11.2 million, or 44% of revenue, up 6% from the first quarter of 2025.
Gross margin fell to 37.6% from 43.1% a year earlier, which Judd attributed primarily to the Irwin acquisition. Irwin has historically operated at lower gross margins than Legacy FitLife, he said. However, gross margins improved sequentially for both Legacy FitLife and Irwin from the fourth quarter of 2025 to the first quarter of 2026.
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Net income was $1.7 million, down from $2.0 million in the prior-year period. Judd said the decline was driven mainly by higher amortization expense and interest expense tied to the Irwin acquisition. Adjusted EBITDA was $3.3 million, down 3% from the first quarter of 2025.
Irwin Acquisition Lifts Sales, Pressures Margins Irwin generated $12.8 million in first-quarter revenue, with $10.3 million, or 80%, coming from wholesale customers and 20% from online sales. Irwin’s gross margin was 34.0%, and contribution as a percentage of revenue was 31.3%.
Judd said FitLife began selling Irwin products on Amazon in mid-October and saw the business scale throughout the fourth quarter. Irwin Amazon revenue reached almost $500,000 in December 2025, approximately $800,000 in March 2026 and approximately $900,000 in April 2026. He said the account continued to grow sequentially in May month to date, though the pace of growth had slowed.
FitLife said Irwin’s organic revenue declined approximately 13% year over year after adjusting for the loss of Costco U.S. and Rite Aid as customers before the acquisition and excluding CBD products because the company decided to exit the CBD market. Judd estimated that $1 million to $1.5 million, or more than half of the decline, was tied to previously discussed out-of-stock issues.
Judd said the company expects Irwin to have additional growth opportunities on Amazon as it resolves out-of-stock situations, sets up listings for products not yet available on the platform and launches Canadian products on Amazon Canada later in the second quarter. He also said Irwin’s Amazon subscriber count increased from roughly 500 at the beginning of the first quarter to approximately 3,600 at quarter-end and more than 5,700 at the time of the call.
Legacy FitLife Revenue Declines Legacy FitLife revenue was $12.5 million, with 70% from online sales and 30% from wholesale customers. Judd said wholesale revenue declined 28% year over year and online revenue fell 18%, producing a 22% decline in total revenue.
The declines were primarily tied to lower online revenue for MRC and lower wholesale revenue from GNC. Judd said the year-over-year wholesale comparison was particularly difficult because the first quarter of 2025 included restocking of GNC distribution centers following the resolution of a previously disclosed commercial dispute that had caused FitLife to stop shipments to GNC.
Legacy FitLife gross margin declined to 41.2% from 43.1% a year earlier, but improved from 40.7% in the fourth quarter of 2025. Contribution declined 27% to $4.3 million, and contribution as a percentage of revenue fell to 34.1% from 36.5%. Sequentially, contribution was approximately flat, while contribution margin improved from 32.5% in the fourth quarter.
Company Reduces Debt FitLife made a scheduled amortization payment of approximately $1.5 million during the quarter, reducing its term loan balance to $37.6 million. The company also paid down an additional $1.4 million on its revolving line of credit, bringing that balance to $4.2 million.
Judd said FitLife intends to continue using excess free cash flow to reduce indebtedness.
Q&A Focuses on Amazon, MusclePharm and Kroger Launch In response to a question from Ryan Meyers of Lake Street Capital Markets, Judd said revenue improved sequentially through the quarter. January was “kind of tough,” February was similar to January but stronger on a revenue-per-day basis, and March was above 9% in terms of revenue, he said. April revenue was higher than January and February but lower than March, though Judd said April was the company’s highest sales order month of the year. He noted that shipment timing affected revenue recognition.
Asked about Irwin’s Amazon potential, Judd said he did not see a reason the business would not reach at least $1 million per month. He cited roughly 20 Irwin products not yet set up for Amazon sales, out-of-stock products that have limited sales on the platform, the opening of Amazon Canada and increased advertising as potential tailwinds.
Sean McGowan of Roth Capital asked about MusclePharm. Judd said MusclePharm revenue was down “by choice,” as FitLife opted not to sell to some large international protein buyers at very low margins. He said online performance had improved from earlier double-digit declines to being down only slightly, and he expects MusclePharm margins to improve because the company is selling less to lower-margin international customers.
Judd also said FitLife is working to adapt to changes in Amazon’s marketplace dynamics by shifting more marketing dollars off Amazon and toward Google Ads, Meta Ads and TikTok. He said the company was “absolutely not declaring victory” but was seeing some positive trends.
FitLife also announced the launch of two MusclePharm liquid L-carnitine SKUs in several hundred Kroger stores nationwide beginning in June. In response to Samir Patel of Askeladden Capital, Judd said the products will be sold in roughly 700 to 800 stores across multiple Kroger banners, including Kroger, Fred Meyer and Smith’s. He said the company plans marketing support including connected TV advertising, possible direct mail and neck-band coupons to encourage trial.
Judd said the Kroger opportunity began before the Irwin acquisition, though FitLife expects synergies from Irwin’s existing relationships and broker network. He said the initiative has been a major focus for the company’s new chief marketing officer and consolidated marketing team.
About FitLife Brands NASDAQ: FTLFFitLife Brands, Inc provides nutritional supplements for health-conscious consumers in the United States and internationally. The company provides weight loss, sports nutrition, and general health products; sports nutrition products; weight loss and sports nutrition products; sports nutrition and general wellness formulations with an emphasis on natural, vegan, and organic ingredients; and male health and weight loss products, as well as other diet, health, and sports nutrition supplements and related products; and value-oriented sports nutrition and weight loss products.
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OMAHA, NE, June 09, 2026 (GLOBE NEWSWIRE) -- FitLife Brands, Inc. (Nasdaq: FTLF), a leader in innovative nutritional supplements and wellness products, today announced a new partnership between Dr. Tobias® and legendary competitive eater Joey Chestnut. The campaign, built around the tagline “Cleanse Like a Winner,” brings together Chestnut’s championship mindset with Dr. Tobias’ focus on everyday wellness and digestive health support.
The collaboration pairs one of the most recognizable names in sports entertainment with Dr. Tobias Colon 14 Day Cleanse in a campaign designed to inspire people to reset routines, stay consistent, and approach wellness with the mindset of a champion.
Known worldwide for his record-breaking performances and larger-than-life personality, Chestnut brings humor, discipline, and authenticity to the partnership – showing fans that even champions know the importance of getting back on track.
“I put my body through a lot when I do competitions and eating challenges. I need to be intentional with what I consume in between. I’ve regularly done cleanses to help me reset and restore my balance. When I discovered Dr. Tobias, it quickly became my favorite. It’s easy and it fits into my routine. This partnership was so authentic and just made too much sense. You don’t have to be a competitive eater to benefit from Dr. Tobias products though. We’re going to have some fun in making people aware of that,” said Chestnut.
The “Cleanse Like a Winner” campaign will roll out across TikTok, Instagram, YouTube, and digital platforms with a mix of comedic content, behind-the-scenes moments, wellness routines, and motivational messaging inspired by Joey’s competitive spirit.
“Joey is disciplined, driven, and genuinely passionate about digestive wellness. He brings the kind of energy, authenticity, and champion mindset we wanted for this campaign,” said Cassie Anderson, Director of Sponsorships. “Together, we’re creating a fresh, entertaining approach to wellness that feels both motivating and approachable.”
The partnership reflects Dr. Tobias’ investment in culturally relevant campaigns that connect wellness with real-life habits and personalities consumers already know and love.
“Joey Chestnut represents commitment and consistency in his approach to holistic wellbeing that aligns perfectly with the Dr. Tobias Colon 14 Day Cleanse,” said Dayton Judd, CEO of FitLife Brands. “This partnership gives us an exciting opportunity to connect with customers in a fresh, entertaining way while reinforcing our focus on gut health and everyday wellness routines.”
The “Cleanse Like a Winner” campaign launches today across Dr. Tobias and Joey Chestnut social channels.
About Dr. Tobias
Dr. Tobias is a wellness brand focused on helping consumers support their everyday health routines through thoughtfully formulated supplements designed for modern lifestyles. Available on DrTobias.com, Amazon, TikTok and more, Dr. Tobias Colon 14 Day Cleanse is a staple in digestive health supplements.
About Joey Chestnut
Joey Chestnut is a world-renowned competitive eater and multiple-time champion recognized globally for his record-breaking performances, larger-than-life personality, and unmatched competitive drive.
About FitLife Brands
FitLife Brands is a developer and marketer of innovative and proprietary nutritional supplements and wellness products for health-conscious consumers. FitLife markets over 500 different products online and through various retail locations. FitLife is headquartered in Omaha, Nebraska. For more information, please visit our website at www.fitlifebrands.com.
Oxford BioMedica (OTCMKTS:OXBDF - Get Free Report) and Immuneering (NASDAQ: IMRX - Get Free Report) are both small-cap medical companies, but which is the better investment? We will compare the two companies based on the strength of their profitability, institutional ownership, analyst recommendations, dividends, risk, earnings and valuation. Volatility and Risk Oxford BioMedica has a beta
NEW YORK, March 17, 2026 (GLOBE NEWSWIRE) -- Immuneering Corporation (Nasdaq: IMRX), a late-stage clinical oncology company focused on keeping cancer patients alive and helping them thrive, today announced it will present a poster on one of the three key mechanisms by which atebimetinib aims to improve overall survival: shrinking tumors durably. The poster will be presented at the American Association for Cancer Research (AACR) Annual Meeting taking place April 17-22, 2026 in San Diego, CA.
Inhibitors of RAS, RAF, or MEK often provide only temporary benefit due to resistance, as tumors acquire new mutations or mechanisms of escape within the MAPK pathway. Atebimetinib, a novel Deep Cyclic Inhibitor of MEK, is engineered to mitigate the selective pressure that typically drives these resistance mechanisms, with the goal of more durable anti-tumor activity. Immuneering will present an analysis of circulating tumor DNA (ctDNA) from ≥64 patients with RAS-mutant solid tumors treated with atebimetinib, showing that acquired MAPK pathway alterations are rarely seen in patients treated with atebimetinib. These findings suggest that Deep Cyclic Inhibitors have the potential to overcome the limitations of conventional MAPK inhibition and provide a more sustained clinical benefit for patients.
Poster Presentation Details:
Title: Atebimetinib’s Deep Cyclic Inhibition of MEK Constrains MAPK-Axis Adaptive and Acquired Alterations in Patients with RAS-Mutant Tumors
Session Category: Experimental and Molecular Therapeutics
Session Title: Targeting Drug Resistance 2: RAS Signaling
Poster Number: 1873
Poster Board Number: 6
Session Date: April 20, 2026
Session Time: 9:00 AM – 12:00 PM ET
Location: Poster Section 19
The abstract will be available on the AACR website. Following presentation, the poster will be available on the publications section of Immuneering’s website at https://immuneering.com/publications.
About Immuneering
Immuneering is a late-stage clinical oncology company focused on keeping cancer patients alive and helping them thrive. The Company is developing an entirely new category of cancer medicines, Deep Cyclic Inhibitors, designed to improve overall survival by three mechanisms: shrinking tumors durably with less resistance, preserving body mass by countering cachexia, and minimizing side effects to maximize performance status and combinability. Immuneering’s lead product candidate, atebimetinib, is an oral, once-daily Deep Cyclic Inhibitor of MEK, designed to improve survival across many cancer indications, including MAPK pathway-driven tumors such as pancreatic cancer. The company expects to dose the first patient in mid-2026 in MAPKeeper 301, a globally randomized pivotal Phase 3 trial evaluating atebimetinib in combination with chemotherapy in first-line pancreatic cancer patients. The Company’s development pipeline also includes additional combination opportunities and early-stage programs. For more information, please visit www.immuneering.com.
Forward-Looking Statements
This press release contains forward-looking statements, including within the meaning of the Private Securities Litigation Reform Act of 1995. All statements contained in this press release that do not relate to matters of historical fact should be considered forward-looking statements, including, without limitation, statements regarding: the treatment potential of atebimetinib, alone or in combination with other agents to treat cancer, including modified Gemcitabine/nab-paclitaxel (mGnP) in first-line pancreatic cancer and its potential to deliver overall survival with both durability and tolerability; the ability of the three design mechanisms of atebimetinib to shrink tumors durably, improve overall survival and overcome the limitations of conventional MAPK inhibition and provide a more sustained clinical benefit for patients.
These forward-looking statements are based on management’s current expectations. These statements are neither promises nor guarantees, but involve known and unknown risks, uncertainties and other important factors that may cause our actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements, including, but not limited to, the following: the risks inherent in oncology drug research and development, including target discovery, target validation, lead compound identification, and lead compound optimization; we have incurred significant losses, are not currently profitable and may never become profitable; our projected cash runway; our need for additional funding; our unproven approach to therapeutic intervention; our ability to address regulatory questions and the uncertainties relating to regulatory filings, reviews and approvals; the lengthy, expensive, and uncertain process of clinical drug development, including potential delays in or failure to obtain regulatory approvals; our reliance on third parties and collaborators to conduct our clinical trials, manufacture our product candidates, and develop and commercialize our product candidates, if approved; failure to compete successfully against other drug companies; protection of our proprietary technology and the confidentiality of our trade secrets; potential lawsuits for, or claims of, infringement of third-party intellectual property or challenges to the ownership of our intellectual property; our patents being found invalid or unenforceable; costs and resources of operating as a public company; and unfavorable or no analyst research or reports.
These and other important factors discussed under the caption “Risk Factors” in our Annual Report on Form 10-K for the period ended December 31, 2025, and our other reports filed with the U.S. Securities and Exchange Commission, could cause actual results to differ materially from those indicated by the forward-looking statements made in this press release. Any such forward-looking statements represent management's estimates as of the date of this press release. While we may elect to update such forward-looking statements at some point in the future, except as required by law, we disclaim any obligation to do so, even if subsequent events cause our views to change. These forward-looking statements should not be relied upon as representing our views as of any date subsequent to the date of this press release.
Shares of Immuneering Corporation (NASDAQ: IMRX - Get Free Report) have earned a consensus rating of "Moderate Buy" from the seven ratings firms that are currently covering the company, Marketbeat reports. One analyst has rated the stock with a sell recommendation, five have given a buy recommendation and one has given a strong buy recommendation to
NEW YORK, April 06, 2026 (GLOBE NEWSWIRE) -- Immuneering Corporation (Nasdaq: IMRX), a late-stage clinical oncology company focused on keeping cancer patients alive and helping them thrive, today announced that Ben Zeskind, Chief Executive Officer, will participate in a fireside chat at the 25th Annual Needham Virtual Healthcare Conference on Monday, April 13, 2026 at 3:45 p.m. ET. The fireside chat will be webcast live and archived in the Investor Relations section of Immuneering’s website at Events & Presentations | Immuneering Corporation.
About Immuneering
Immuneering is a late-stage clinical oncology company focused on keeping cancer patients alive and helping them thrive. The Company is developing an entirely new category of cancer medicines, Deep Cyclic Inhibitors, designed to improve overall survival by three mechanisms: shrinking tumors durably with less resistance, preserving body mass by countering cachexia, and minimizing side effects to maximize performance status and combinability. Immuneering’s lead product candidate, atebimetinib, is an oral, once-daily Deep Cyclic Inhibitor of MEK, designed to improve survival across many cancer indications, including MAPK pathway-driven tumors such as pancreatic cancer. The company expects to dose the first patient in mid-2026 in MAPKeeper 301, a globally randomized pivotal Phase 3 trial evaluating atebimetinib in combination with chemotherapy in first-line pancreatic cancer patients. The Company’s development pipeline also includes additional combination opportunities and early-stage programs. For more information, please visit www.immuneering.com.
Immuneering (NASDAQ:IMRX) CEO Benjamin J. Zeskind told investors at a Needham conference session that 2026 has started with what he described as “extraordinary” early survival results for the company’s lead program, atebimetinib, in first-line pancreatic cancer, and outlined multiple upcoming clinical and regulatory milestones across pancreatic and lung cancer.
Phase II pancreatic cancer survival update and near-term catalysts Zeskind said the company reported in January a 12-month overall survival (OS) rate of 64% in first-line pancreatic cancer patients treated with atebimetinib in combination with chemotherapy, with median OS not yet reached at the time of that cutoff. He said the dataset had a 13.4-month median follow-up and included 34 patients, exceeding the original enrollment goal of 30.
He also highlighted a cross-trial comparison against the pivotal MPACT study for gemcitabine/nab-paclitaxel (GNP), which he cited as having shown 35% 12-month OS. Zeskind emphasized that Immuneering’s survival curves “separate early” and remain separated at six, nine, and 12 months based on the company’s updates.
Looking ahead, Zeskind reiterated guidance for another survival update in the first half of the year based on an expanded cohort “of more than 50 patients,” describing it as the original 34 patients plus “another 20 or so.” He said the company previously indicated OS in the expanded cohort was “trending consistently” with the initial 34-patient cohort, while declining to provide additional specifics ahead of the planned update.
Beyond OS, he pointed to previously reported progression-free survival (PFS) of 8.5 months, which he said was “about three months better” than the standard-of-care benchmark, along with tolerability results. He said only two categories of grade 3 adverse events occurred in more than 10% of patients—neutropenia and anemia—which he associated with the chemotherapy backbone and said were not observed in monotherapy.
Zeskind also noted the phase II population skewed older than historical pivotal studies: he cited a median age of 69, with more than two-thirds of patients over 65.
Mechanism: “Deep Cyclic Inhibition” and a three-part survival thesis Zeskind contrasted atebimetinib with traditional targeted therapies that aim for continuous pathway suppression, describing Immuneering’s approach as “Deep Cyclic Inhibition.” He said the company designed atebimetinib to deliver intense pulses of MAP kinase pathway inhibition—spiking rapidly to high concentration, shutting down signaling above the IC90, and then clearing quickly due to a short half-life—resulting in pathway “release” by the end of the day before the next dose.
He attributed this profile to novel chemistry that provides a “fast off rate” and supports once-daily oral dosing for patients. Conceptually, he said the intermittent pressure is intended to prevent the rapid selection of resistant cancer cell populations predicted by Darwinian models of tumor evolution, referencing work by Moffitt Cancer Center’s Robert Gatenby. Zeskind characterized the intended effect as keeping sensitive and resistant cells “fighting each other,” calling it a tumor “civil war.”
He said the company believes survival benefits may be driven by three mechanisms:
Durable tumor control: long, slow, steady reductions rather than rapid shrinkage followed by resistance. Body mass preservation: Improved tolerability: To support the importance of weight stability and tolerability, Zeskind cited literature-based hazard ratios, including 1.55 for patients who lose weight versus those stable or gaining, 1.48 when performance status declines to ECOG 2, and 1.51 for patients unable to receive second-line therapy.
Why first-line pancreatic cancer is the priority In response to a question about differences between first-line and second-line activity, Zeskind said Immuneering has prioritized first-line pancreatic cancer because “that’s where the most patients are,” estimating there are twice as many patients in the first-line setting as in later lines and noting many do not reach later lines. He also pointed to the need to combine with chemotherapy in first line and said atebimetinib’s tolerability has enabled combination treatment.
He added that for first-line chemotherapies, the “primary resistance pathway is the MAP kinase pathway,” suggesting this biology may be relevant when thinking about line-of-therapy dynamics.
Phase III MAPKeeper-301: design, timing, and regulatory focus Zeskind outlined Immuneering’s planned pivotal trial, MAPKeeper-301, calling it a “global randomized pivotal study” comparing atebimetinib plus modified GNP chemotherapy versus standard-of-care GNP, with OS as the primary endpoint. He said the trial will enroll “a little over 500 patients.”
He also referenced a December announcement of “regulatory alignment,” said the study is “fully funded,” and reiterated guidance to dose the first patient mid-year. On timing, he pushed back on discussing interim PFS timelines and said the company is guiding to a top-line readout “about two years after that first patient dose.”
On the chemotherapy landscape, Zeskind said use in the real world is “about 50/50” between gemcitabine-containing regimens and FOLFIRINOX/NALIRIFOX, describing gemcitabine regimens as better tolerated and the others as harsher but offering some survival advantage. He said Immuneering selected modified GNP (every-other-week dosing) based on work by Mayo Clinic investigators Daniel H. Ahn and Tanios Bekaii-Saab showing improved tolerability without a significant survival difference versus standard scheduling.
He added the company also has a phase II arm combining atebimetinib with FOLFIRINOX, and described a case discussed by Weill Cornell’s Allyson J. Ocean involving a “confirmed complete response,” while noting aggregate data have not yet been shared.
Competitive commentary and AACR ctDNA poster Asked about competition, Zeskind discussed the company’s view of Revolution Medicines’ program and said Immuneering has urged the company to release additional first-line pancreatic cancer data—particularly overall survival and other endpoints—to allow more transparent comparisons, while acknowledging cross-trial caveats. Zeskind compared disclosed tolerability metrics, stating Immuneering’s reported adverse-event profile appears different from what Revolution has reported in first line, and argued that comparisons should use consistent denominators when assessing response rates.
Zeskind also previewed an upcoming AACR presentation focused on acquired alterations detected in circulating tumor DNA (ctDNA). He said Immuneering has previously observed “very few acquired alterations in the MAP kinase pathway” in phase I, which he believes supports the idea that atebimetinib may avoid driving common on-pathway resistance mechanisms seen with mutation-specific RAS inhibitors or pan-RAS approaches. He said the company’s AACR press release indicated a similar conclusion from the upcoming dataset.
About Immuneering (NASDAQ:IMRX) Immuneering (Nasdaq: IMRX) is a clinical-stage biopharmaceutical company leveraging artificial intelligence and its proprietary RABIT (Repurposing and Accelerating Biotechnology Tools) platform to design and optimize small-molecule and peptide therapies. By analyzing large-scale biomedical datasets, Immuneering’s machine learning algorithms identify novel drug–target interactions, repurpose existing drug scaffolds and accelerate lead candidate selection. The company’s AI-driven approach aims to reduce development timelines and improve therapeutic profiles in areas of high unmet medical need.
The company’s lead program, IRX-2, is a small-molecule candidate currently in Phase 2 clinical trials for the treatment of painful diabetic peripheral neuropathy.
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Analysis of circulating tumor DNA from atebimetinib-treated patients shows acquired MAPK pathway alterations are rare, supporting observed durable first-line activity
Atebimetinib-treated tumors rarely acquire the genetic alterations most commonly associated with resistance to RAS inhibitors, providing molecular rationale to treat with atebimetinib early
NEW YORK, April 20, 2026 (GLOBE NEWSWIRE) -- Immuneering Corporation (Nasdaq: IMRX), a late-stage clinical oncology company focused on keeping cancer patients alive and helping them thrive, today announced the presentation of new genetic data at the 2026 American Association for Cancer Research (AACR) Annual Meeting taking place April 17-22, 2026 in San Diego, CA.
“Atebimetinib is designed to promote survival by three mechanisms: shrinking tumors durably, preserving body mass by counteracting muscle wasting, and maintaining performance status by maximizing tolerability,” said Ben Zeskind, Ph.D., Chief Executive Officer of Immuneering. “We believe these characteristics have the potential to both yield the best survival in the first-line, and to give patients the best chance of reaching and benefitting from second-line treatment. Today’s data at AACR add genetic rationale to support atebimetinib’s observed durable tumor shrinkage and its optimal use in the first-line setting by showing that the most common RAS-inhibitor resistance mechanisms are rarely seen in atebimetinib-treated patients.”
Inhibitors of RAS, RAF, or MEK often provide only temporary benefit due to pervasive resistance, as tumors acquire new mutations or mechanisms of escape within the MAPK pathway. Atebimetinib, a novel Deep Cyclic Inhibitor of MEK, is engineered to mitigate the selective pressure that typically drives these resistance mechanisms, with the goal of more durable anti-tumor activity. Immuneering presented circulating tumor DNA (ctDNA) data from 123 patients treated with atebimetinib, showing that acquired MAPK pathway alterations are rarely seen. These findings suggest that Deep Cyclic Inhibitors have the potential to overcome the limitations of conventional MAPK inhibition and provide a more sustained clinical benefit for patients, while potentially preserving sensitivity to subsequent treatments.
Key Findings from the AACR Presentation:
Rare MAPK pathway reactivation: Across 86 patients treated with atebimetinib monotherapy and 37 patients treated in combination with chemotherapy, emergent and acquired mutations rarely converged on the RAS/MAPK pathway, in contrast to what is commonly observed with chronic RAS-targeted therapies.Diffuse, non-convergent resistance patterns: Emergent resistance following atebimetinib treatment utilized a variety of non-MAPK pathways, rather than converging on a single escape mechanism.Limited early adaptive resistance: ctDNA analysis showed minimal early molecular evolution during treatment, indicating that atebimetinib is not driving adaptive resistance and may impose less selective pressure than continuous pathway inhibition.Taken together, the data position atebimetinib as a differentiated MEK inhibitor with potential to drive deep and durable antitumor activity. “Our AACR data further validate the scientific foundation of our platform, demonstrating that Deep Cyclic Inhibition can fundamentally alter how tumors evolve under therapy, unlocking opportunities to improve treatment durability,” said Brett Hall, Ph.D., Chief Scientific Officer of Immuneering. “Deep Cyclic Inhibition of MEK avoids the continuous selective pressure that typically drives tumors to become resistant to treatment via reactivation of the MAPK pathway. This, combined with atebimetinib’s tolerability profile, has the potential to improve depth and durability of response in a broad range of cancers, starting with first-line pancreatic cancer.”
Poster Presentation Details:
Title: Atebimetinib’s Deep Cyclic Inhibition of MEK Constrains MAPK-Axis Adaptive and Acquired Alterations in Patients with RAS-Mutant Tumors
Session Category: Experimental and Molecular Therapeutics
Session Title: Targeting Drug Resistance 2: RAS Signaling
Poster Number: 1873
Poster Board Number: 6
Session Date: April 20, 2026
Session Time: 9:00 AM – 12:00 PM ET
Location: Poster Section 19
The poster is available on the publications section of Immuneering’s website at https://immuneering.com/publications.
Immuneering has guided to dosing the first patient in its pivotal Phase 3 MAPKeeper 301 trial of atebimetinib plus modified gemcitabine/nab-paclitaxel (mGnP) in patients with first-line metastatic pancreatic cancer in mid-2026. In the second half of the year, the company expects to dose the first patient in a Phase 2 trial of atebimetinib plus Libtayo® in patients with first-line RAS-mutant non-small cell lung cancer.
About Immuneering
Immuneering is a late-stage clinical oncology company focused on keeping cancer patients alive and helping them thrive. The Company is developing an entirely new category of cancer medicines, Deep Cyclic Inhibitors, designed to improve overall survival by three mechanisms: shrinking tumors durably with less resistance, preserving body mass by countering cachexia, and minimizing side effects to maximize performance status and combinability. Immuneering’s lead product candidate, atebimetinib, is an oral, once-daily Deep Cyclic Inhibitor of MEK, designed to improve survival across many cancer indications, including MAPK pathway-driven tumors such as pancreatic cancer. The company expects to dose the first patient in mid-2026 in MAPKeeper 301, a globally randomized pivotal Phase 3 trial evaluating atebimetinib in combination with chemotherapy in first-line pancreatic cancer patients. The Company’s development pipeline also includes additional combination opportunities and early-stage programs. For more information, please visit www.immuneering.com.
Forward-Looking Statements
This press release contains forward-looking statements, including within the meaning of the Private Securities Litigation Reform Act of 1995. All statements contained in this press release that do not relate to matters of historical fact should be considered forward-looking statements, including, without limitation, statements regarding: the treatment potential of atebimetinib, alone or in combination with other agents to treat cancer, including modified Gemcitabine/nab-paclitaxel (mGnP) in first-line pancreatic cancer and its potential to deliver overall survival with both durability and tolerability; the timing of dosing of additional studies, the ability of the three design mechanisms of atebimetinib to shrink tumors durably, improve overall survival and overcome the limitations of conventional MAPK inhibition, including to impose less selective pressure, and provide a more sustained clinical benefit for patients.
These forward-looking statements are based on management’s current expectations. These statements are neither promises nor guarantees, but involve known and unknown risks, uncertainties and other important factors that may cause our actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements, including, but not limited to, the following: the risks inherent in oncology drug research and development, including target discovery, target validation, lead compound identification, and lead compound optimization; we have incurred significant losses, are not currently profitable and may never become profitable; our projected cash runway; our need for additional funding; our unproven approach to therapeutic intervention; our ability to address regulatory questions and the uncertainties relating to regulatory filings, reviews and approvals; the lengthy, expensive, and uncertain process of clinical drug development, including potential delays in or failure to obtain regulatory approvals; our reliance on third parties and collaborators to conduct our clinical trials, manufacture our product candidates, and develop and commercialize our product candidates, if approved; failure to compete successfully against other drug companies; protection of our proprietary technology and the confidentiality of our trade secrets; potential lawsuits for, or claims of, infringement of third-party intellectual property or challenges to the ownership of our intellectual property; our patents being found invalid or unenforceable; costs and resources of operating as a public company; and unfavorable or no analyst research or reports.
These and other important factors discussed under the caption “Risk Factors” in our Annual Report on Form 10-K for the period ended December 31, 2025, and our other reports filed with the U.S. Securities and Exchange Commission, could cause actual results to differ materially from those indicated by the forward-looking statements made in this press release. Any such forward-looking statements represent management's estimates as of the date of this press release. While we may elect to update such forward-looking statements at some point in the future, except as required by law, we disclaim any obligation to do so, even if subsequent events cause our views to change. These forward-looking statements should not be relied upon as representing our views as of any date subsequent to the date of this press release.
- New data from Phase 2a clinical trial evaluating atebimetinib + mGnP in first-line pancreatic cancer will be presented in an oral session by Dr. Peter Vu, UC San Diego Health -
- The ASCO presentation will highlight data from an expanded cohort totaling 55 first-line patients -
NEW YORK, April 21, 2026 (GLOBE NEWSWIRE) -- Immuneering Corporation (Nasdaq: IMRX), a late-stage clinical oncology company focused on keeping cancer patients alive and helping them thrive, today announced that updated data from the Phase 2a clinical trial evaluating atebimetinib (IMM-1-104) in combination with modified gemcitabine/nab-paclitaxel (mGnP) in first-line pancreatic cancer patients will be presented as an oral presentation at the 2026 American Society of Clinical Oncology (ASCO) Annual Meeting, taking place May 29 – June 2, 2026, in Chicago, IL.
The oral presentation will highlight data from an expanded cohort totaling 55 first-line patients, which includes the initial cohort of 34 patients that the company previously reported plus an additional 21 patients.
“We are excited to present new survival data from an expanded cohort of 55 first-line pancreatic cancer patients treated with atebimetinib in combination with mGnP in an oral presentation at ASCO,” said Ben Zeskind, Ph.D., CEO of Immuneering. “Atebimetinib was designed with three distinct mechanisms to promote survival: shrinking tumors durably, preserving body mass, and maximizing tolerability. We believe these mechanisms have the potential to both yield the best survival in the first-line setting, and to give patients the best chance of reaching and benefitting from second-line treatment. We look forward to sharing this updated dataset in first-line pancreatic cancer patients as we pursue our mission to help patients survive and thrive.”
Oral Presentation Details:
Title: Results from a phase 2a study of atebimetinib in combination with mGnP in advanced or metastatic pancreatic cancer
Session Type/Title: Rapid Oral Abstract Session – Gastrointestinal Cancer – Gastroesophageal, Pancreatic, and Hepatobiliary
Abstract Number: 4013
Date and Time: June 1, 2026, 1:15 p.m. – 2:45 p.m. CDT
Presenter: Peter Vu, MD, MHA
About Immuneering
Immuneering is a late-stage clinical oncology company focused on keeping cancer patients alive and helping them thrive. The Company is developing an entirely new category of cancer medicines, Deep Cyclic Inhibitors, designed to improve overall survival by three mechanisms: shrinking tumors durably with less resistance, preserving body mass by countering cachexia, and minimizing side effects to maximize performance status and combinability. Immuneering’s lead product candidate, atebimetinib, is an oral, once-daily Deep Cyclic Inhibitor of MEK, designed to improve survival across many cancer indications, including MAPK pathway-driven tumors such as pancreatic cancer. The company expects to dose the first patient in mid-2026 in MAPKeeper 301, a globally randomized pivotal Phase 3 trial evaluating atebimetinib in combination with chemotherapy in first-line pancreatic cancer patients. The Company’s development pipeline also includes additional combination opportunities and early-stage programs. For more information, please visit www.immuneering.com.
Forward-Looking Statements
This press release contains forward-looking statements, including within the meaning of the Private Securities Litigation Reform Act of 1995. All statements contained in this press release that do not relate to matters of historical fact should be considered forward-looking statements, including, without limitation, statements regarding: the treatment potential of atebimetinib, alone or in combination with other agents to treat cancer, including modified Gemcitabine/nab-paclitaxel (mGnP) in first-line pancreatic cancer and its potential to deliver overall survival with both durability and tolerability; the timing of dosing of the MAPKeeper 301 study; the content of the upcoming 2026 oral presentation at ASCO; the ability of the three design mechanisms of atebimetinib to shrink tumors durably, improve overall survival and overcome the limitations of conventional MAPK inhibition and provide a more sustained clinical benefit for patients.
These forward-looking statements are based on management’s current expectations. These statements are neither promises nor guarantees, but involve known and unknown risks, uncertainties and other important factors that may cause our actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements, including, but not limited to, the following: the risks inherent in oncology drug research and development, including target discovery, target validation, lead compound identification, and lead compound optimization; we have incurred significant losses, are not currently profitable and may never become profitable; our projected cash runway; our need for additional funding; our unproven approach to therapeutic intervention; our ability to address regulatory questions and the uncertainties relating to regulatory filings, reviews and approvals; the lengthy, expensive, and uncertain process of clinical drug development, including potential delays in or failure to obtain regulatory approvals; our reliance on third parties and collaborators to conduct our clinical trials, manufacture our product candidates, and develop and commercialize our product candidates, if approved; failure to compete successfully against other drug companies; protection of our proprietary technology and the confidentiality of our trade secrets; potential lawsuits for, or claims of, infringement of third-party intellectual property or challenges to the ownership of our intellectual property; our patents being found invalid or unenforceable; costs and resources of operating as a public company; and unfavorable or no analyst research or reports.
These and other important factors discussed under the caption “Risk Factors” in our Annual Report on Form 10-K for the period ended December 31, 2025, and our other reports filed with the U.S. Securities and Exchange Commission, could cause actual results to differ materially from those indicated by the forward-looking statements made in this press release. Any such forward-looking statements represent management's estimates as of the date of this press release. While we may elect to update such forward-looking statements at some point in the future, except as required by law, we disclaim any obligation to do so, even if subsequent events cause our views to change. These forward-looking statements should not be relied upon as representing our views as of any date subsequent to the date of this press release.
Immuneering Corporation (IMRX) presents promising early data in frontline metastatic pancreatic cancer with its MEK inhibitor atebimetinib, benchmarking favorably against Revolution Medicines. IMRX's 12-month overall survival rate of 64% in a small phase 2a trial compares well to historical controls and competitive agents, but caution is warranted due to trial size. The company maintains over $200 million in liquidity, supporting a cash runway into 2029, though future trial costs may shorten this horizon.
- New survival data from Phase 2a clinical trial evaluating atebimetinibmGnP in first-line metastatic pancreatic cancer to be presented in an oral session at 2026 ASCO Annual Meeting - - Pivotal Phase 3 MAPKeeper 301 trial of atebimetinibmGnP in first-line metastatic pancreatic cancer now recruiting (NCT07562152),with first patient dosing on track for mid-2026 - - 27 months progression-free survival to date in a third-line pancreatic cancer patient receiving atebimetinib monotherapy, with an ongoing 85% reduction in tumor burden - - Ended Q1 2026 with $198.
- Detailed data from 55 patients to be shared in an oral presentation at the ASCO Annual Meeting on June 1, 2026 -
- Tolerability profile consistent with prior updates: only two categories of Grade 3 or higher treatment-related adverse events observed in ≥10% of patients, both chemotherapy-related -
- Company to hold investor conference call on June 1, 2026, at 8:00 a.m. EST -
NEW YORK, May 21, 2026 (GLOBE NEWSWIRE) -- Immuneering Corporation (Nasdaq: IMRX), a late-stage clinical oncology company focused on keeping cancer patients alive and helping them thrive, today reported a 17.3-month median overall survival (OS) in first-line metastatic pancreatic cancer patients treated in its Phase 2a clinical trial evaluating atebimetinib (IMM-1-104) plus modified gemcitabine/nab-paclitaxel (mGnP), as of the April 24, 2026 data cutoff date. The only treatment-related adverse events observed at Grade 3 or higher in ≥10% of patients were anemia (16%) and neutropenia (18%), both chemotherapy-related. The full data (N=55) including details on OS, progression free survival (PFS), response, safety, weight stability/gain, and other relevant information will be shared in an oral presentation at the 2026 American Society of Clinical Oncology (ASCO) Annual Meeting by Peter Vu, MD, MHA of UC San Diego Health, on June 1, 2026, at 1:15 p.m. CDT.
“In my own patients on this trial, I have seen meaningful benefit without the functional decline I am accustomed to seeing in this disease — patients holding their weight, their energy, and their sense of themselves across many months of treatment," said Daniel Ahn, D.O., Mayo Clinic Arizona, an investigator on the Phase 2a trial of atebimetinib. "When the field has more than one effective first-line option, the deciding factor at the bedside will be tolerability.”
“A 17.3-month median overall survival is a meaningful result for first-line metastatic pancreatic cancer patients,” said Ben Zeskind, Ph.D., CEO of Immuneering. “Importantly, only two categories of Grade 3 or higher treatment-related adverse events were observed in 10% or more of patients, both chemotherapy-related. These findings support our randomized Phase 3 clinical trial, MAPKeeper 301, which is now recruiting. We look forward to Dr. Vu’s presentation of the full data at ASCO on June 1.”
The company will share data from the expanded cohort totaling 55 first-line patients at ASCO on June 1, 2026, which includes an initial cohort of 34 patients that the company previously reported, plus an additional 21 patients. The company’s pivotal Phase 3 MAPKeeper 301 (NCT07562152) trial of atebimetinib + mGnP in patients with first-line metastatic pancreatic cancer is currently recruiting, and the company is on track to dose the first patient in mid-2026.
Oral Presentation Details:
Title: Results from a phase 2a study of atebimetinib in combination with mGnP in advanced or metastatic pancreatic cancer
Session Type/Title: Rapid Oral Abstract Session – Gastrointestinal Cancer – Gastroesophageal, Pancreatic, and Hepatobiliary
Abstract Number: 4013
Date and Time: June 1, 2026, 1:15 p.m. – 2:45 p.m. CDT
Presenter: Peter Vu, M.D., MHA (UCSD)
Authors: Vincent Chung (City of Hope), Peter Vu (UCSD), Vincent Ma (University of Wisconsin), Nataliya Uboha (University of Wisconsin), Umair Majeed (Mayo Clinic), Su Chandra (Northwestern), Devalingam Mahalingam (Northwestern), Melissa Johnson (Sarah Cannon), Meredith Pelster (Sarah Cannon), Anna Pavlick (Weill Cornell), Allyson Ocean (Weill Cornell), Barbara Ma (Weill Cornell), Alex Spira (NEXT Oncology), Steven Duffy (HOACNY), Jason Henry (Sarah Cannon), Gregory Botta (UCSD), Alexander Philipovskiy (Sarah Cannon), Shubham Pant (MD Anderson), Sant Chawla (Sarcoma Oncology), Jenny Zhang (Immuneering), Jason Kim (Immuneering), Sarah Kolitz (Immuneering), Jason Funt (Immuneering), Vinny Hayreh (Immuneering), Brett Hall (Immuneering), Ben Zeskind (Immuneering), Igor Matushansky (Immuneering), Daniel Ahn (Mayo Clinic)
Conference Call
Immuneering will host a conference call and live webcast at 8:00 a.m. ET / 7:00 a.m. CT on June 1, 2026, to discuss the data. Individuals interested in listening to the live conference call may do so by dialing (800) 715-9871 for U.S callers and (646) 307-1963 for other locations and reference conference ID 7597768, or from the webcast link in the “investors” section of the company's website at www.immuneering.com. A webcast replay will be available in the investor relations section on the company’s website for 90 days following the completion of the call.
About Immuneering
Immuneering is a late-stage clinical oncology company dedicated to keeping cancer patients alive and helping them thrive, with an initial focus on patients with RAS, RAF, and other MAPK-driven cancers. The Company is developing an entirely new category of cancer medicines, Deep Cyclic Inhibitors, designed to improve overall survival by three mechanisms: shrinking tumors durably with less resistance, preserving body mass by countering cachexia, and minimizing side effects to maximize performance status and combinability. Immuneering’s lead product candidate, atebimetinib, is an investigational, oral, once-daily Deep Cyclic Inhibitor of MEK, designed to improve survival across many cancer indications. The company is conducting a global randomized pivotal trial, MAPKeeper 301, evaluating atebimetinib in combination with chemotherapy in first-line pancreatic cancer patients. The Company’s development pipeline also includes additional combination opportunities and preclinical stage programs. For more information, please visit www.immuneering.com.
Forward-Looking Statements
This press release contains forward-looking statements, including within the meaning of the Private Securities Litigation Reform Act of 1995. All statements contained in this press release that do not relate to matters of historical fact should be considered forward-looking statements, including, without limitation, statements regarding: the treatment potential of atebimetinib, alone or in combination with other agents to treat cancer, including modified Gemcitabine/nab-paclitaxel (mGnP) in first-line pancreatic cancer; the timing of dosing of the MAPKeeper 301 study and the phase 2a results supporting such study; the content of the upcoming 2026 oral presentation at ASCO; the ability of the three design mechanisms of atebimetinib to shrink tumors durably, improve overall survival and overcome the limitations of conventional MAPK inhibition and provide a more sustained clinical benefit for patients.
These forward-looking statements are based on management’s current expectations. These statements are neither promises nor guarantees, but involve known and unknown risks, uncertainties and other important factors that may cause our actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements, including, but not limited to, the following: the risks inherent in oncology drug research and development, including target discovery, target validation, lead compound identification, and lead compound optimization; we have incurred significant losses, are not currently profitable and may never become profitable; our projected cash runway; our need for additional funding; our unproven approach to therapeutic intervention; our ability to address regulatory questions and the uncertainties relating to regulatory filings, reviews and approvals; the lengthy, expensive, and uncertain process of clinical drug development, including potential delays in activating trial sites or enrolling trial participants, or failure to obtain regulatory approvals; our reliance on third parties and collaborators to conduct our clinical trials, manufacture our product candidates, and develop and commercialize our product candidates, if approved; failure to compete successfully against other drug companies; protection of our proprietary technology and the confidentiality of our trade secrets; potential lawsuits for, or claims of, infringement of third-party intellectual property or challenges to the ownership of our intellectual property; our patents being found invalid or unenforceable; costs and resources of operating as a public company; and unfavorable or no analyst research or reports.
These and other important factors discussed under the caption “Risk Factors” in our Quarterly Report on Form 10-Q for the period ended March 31, 2026, and our other reports filed with the U.S. Securities and Exchange Commission, could cause actual results to differ materially from those indicated by the forward-looking statements made in this press release. Any such forward-looking statements represent management's estimates as of the date of this press release. While we may elect to update such forward-looking statements at some point in the future, except as required by law, we disclaim any obligation to do so, even if subsequent events cause our views to change. These forward-looking statements should not be relied upon as representing our views as of any date subsequent to the date of this press release.
- 17.3 months median overall survival in 55 first-line pancreatic cancer patients; vs. 8.5 months for standard of care chemotherapy in the pivotal MPACT study -
- Only two categories of Grade 3+ treatment-related adverse events occurring in ≥10% of patients, both chemotherapy related -
- 84% of participants maintained or gained weight at three months -
- Global Phase 3 MAPKeeper 301 trial (NCT07562152) in first-line metastatic pancreatic cancer actively recruiting, with first patient dosing expected in mid-2026 -
- Company to hold investor conference call today, at 8:00 a.m. EDT -
NEW YORK, June 01, 2026 (GLOBE NEWSWIRE) -- Immuneering Corporation (Nasdaq: IMRX), a late-stage clinical oncology company focused on keeping cancer patients alive and helping them thrive, today announced updated clinical data from its ongoing Phase 2a trial evaluating atebimetinib in combination with modified gemcitabine/nab-paclitaxel (mGnP) in first-line metastatic pancreatic ductal adenocarcinoma (mPDAC).
The data are being presented in an oral session at the 2026 American Society of Clinical Oncology (ASCO) Annual Meeting (see Abstract #4013 and accompanying presentation) by Peter Vu, M.D., M.H.A., Associate Professor of Medicine and Medical Director, Cancer Quality, GI Medical Oncology, Experimental Therapeutics & Cellular and Regenerative Medicine at UC San Diego Moores Cancer Center. The presentation showcases data from an expanded cohort totaling 55 first-line pancreatic cancer patients.
“As pancreatic cancer clinicians, we are urgently seeking therapies capable of meaningfully extending survival while preserving patients’ quality of life,” said Daniel Ahn, D.O., Mayo Clinic Arizona, an investigator on the Phase 2a trial of atebimetinib. “The median overall survival of 17.3 months observed in this study is incredibly encouraging relative to historical outcomes in first-line metastatic pancreatic cancer. Equally important, atebimetinib demonstrated a notably favorable tolerability profile, with limited severe treatment-related toxicities and encouraging indicators of preserved functional status, including weight stability – key characteristics for treatments balancing durable clinical benefit and patient experience. Data from this expanded cohort reinforce atebimetinib’s strong potential in first-line pancreatic cancer.”
This open-label, single-arm Phase 2a trial evaluated atebimetinib at 320 mg once daily in combination with mGnP in participants with first-line metastatic pancreatic cancer, irrespective of mutational status. The Company reported the following as of the April 24, 2026 data cutoff date:
In the expanded 55-patient cohort, median overall survival was 17.3 months (95% CI: 11.2, not reached), compared to 8.5 months median overall survival in the pivotal Phase 3 MPACT study of standard of care gemcitabine/nab-paclitaxel (Von Hoff et al, NEJM, 2013). The median follow-up was 11.6 months.Median progression-free survival was 8.3 months (95% CI: 5.9, 9.6), disease control rate (DCR) was 82%, and the confirmed overall response rate (ORR) was 36%.In the original 34-patient cohort with longer follow-up (median 17.0 months), median overall survival was also observed to be 17.3 months (95% CI: 11.6, not reached) — supporting the consistency of the survival signal across cohorts with different durations of follow-up.
“The data presented at ASCO further strengthen our conviction that atebimetinib has the potential to redefine what it means to live with metastatic pancreatic cancer,” said Ben Zeskind, Ph.D., Co-founder and Chief Executive Officer of Immuneering. “The combination of compelling survival data and a highly favorable safety profile supports the evaluation of this regimen in our Phase 3 study for first-line pancreatic cancer patients, which is now recruiting. We believe the ability of our deep cyclic MEK inhibitors to improve overall survival, while maintaining tolerability, may represent an important advancement for patients and physicians alike.”
Only two categories of Grade 3 or higher treatment-related adverse events occurred in at least 10% of participants, both related to chemotherapy. No Grade 4 adverse events related to atebimetinib and no Grade 5 treatment-related adverse events were reported. Only one participant discontinued atebimetinib while continuing mGnP. The safety profile observed in the trial compared favorably to historical experiences with intensive chemotherapy treatments and combination regimens under development in pancreatic cancer.
Additionally, 84% of participants with available data maintained or gained weight at three months, a potentially important indicator of preserved performance status and tolerability in this patient population where cachexia is common and correlated with poorer outcomes.
Immuneering is currently recruiting patients in MAPKeeper 301 (NCT07562152), a global randomized Phase 3 pivotal trial evaluating atebimetinib plus mGnP versus standard-of-care gemcitabine/nab-paclitaxel in first-line metastatic pancreatic cancer. The trial’s primary endpoint is overall survival.
Upcoming Milestones
Mid 2026: First patient dosed in Phase 3 MAPKeeper 301 trial.2H 2026: First patient dosed in Phase 2 trial of atebimetinib + anti-PD-1 (cemiplimab) in non-small cell lung cancer.Q4 2026: Additional preclinical data supporting atebimetinib + anti-PD-1 in non-small cell lung cancer.Mid 2027: Begin IND-enabling studies for next DCI drug program.Late 2027: Preliminary Phase 2 data: atebimetinib + anti-PD-1 (cemiplimab) in non-small cell lung cancer.Mid 2028: Phase 3 MAPKeeper 301 topline readout expected. Conference Call
Immuneering will host a conference call and live webcast at 8:00 a.m. EDT / 7:00 a.m. CDT on June 1, 2026, to discuss the data. Individuals interested in listening to the live conference call may do so by dialing (800) 715-9871 for U.S. callers and (646) 307-1963 for other locations and reference conference ID 7597768, or from the webcast link in the “investors” section of the company's website at www.immuneering.com. A webcast replay will be available in the investor relations section on the company’s website for 90 days following the completion of the call.
About Immuneering
Immuneering is a late-stage clinical oncology company dedicated to keeping cancer patients alive and helping them thrive, with an initial focus on patients with RAS, RAF, and other MAPK-driven cancers. The Company is developing an entirely new category of cancer medicines, Deep Cyclic Inhibitors, designed to improve overall survival by three mechanisms: shrinking tumors durably with less resistance, preserving body mass by countering cachexia, and minimizing side effects to maximize performance status and combinability. Immuneering’s lead product candidate, atebimetinib, is an investigational, oral, once-daily Deep Cyclic Inhibitor of MEK, designed to improve survival across many cancer indications. The company is conducting a global randomized pivotal trial, MAPKeeper 301, evaluating atebimetinib in combination with chemotherapy in first-line pancreatic cancer patients. The Company’s development pipeline also includes additional combination opportunities and preclinical stage programs. For more information, please visit www.immuneering.com.
Forward-Looking Statements
This press release contains forward-looking statements, including within the meaning of the Private Securities Litigation Reform Act of 1995. All statements contained in this press release that do not relate to matters of historical fact should be considered forward-looking statements, including, without limitation, statements regarding: the treatment potential of atebimetinib, alone or in combination with other agents to treat cancer, including modified Gemcitabine/nab-paclitaxel (mGnP) in first-line pancreatic cancer; the timing of dosing of the MAPKeeper 301 study and the timing of topline results from the study; the timing of dosing of the Phase 2 combination study of atebimetinib in non-small cell lung cancer, including the timing of preliminary results from the study; timing of IND-enabling studies from the next DCI drug program; the ability of phase 2 results presented at ASCO to translate to success and support evaluation in the Company’s phase 3 study; the ability of the three design mechanisms of atebimetinib to shrink tumors durably, improve overall survival and overcome the limitations of conventional MAPK inhibition and provide a more sustained clinical benefit for patients.
These forward-looking statements are based on management’s current expectations. These statements are neither promises nor guarantees, but involve known and unknown risks, uncertainties and other important factors that may cause our actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements, including, but not limited to, the following: the risks inherent in oncology drug research and development, including target discovery, target validation, lead compound identification, and lead compound optimization; we have incurred significant losses, are not currently profitable and may never become profitable; our projected cash runway; our need for additional funding; our unproven approach to therapeutic intervention; our ability to address regulatory questions and the uncertainties relating to regulatory filings, reviews and approvals; the lengthy, expensive, and uncertain process of clinical drug development, including potential delays in activating trial sites or enrolling trial participants, or failure to obtain regulatory approvals; our reliance on third parties and collaborators to conduct our clinical trials, manufacture our product candidates, and develop and commercialize our product candidates, if approved; failure to compete successfully against other drug companies; protection of our proprietary technology and the confidentiality of our trade secrets; potential lawsuits for, or claims of, infringement of third-party intellectual property or challenges to the ownership of our intellectual property; our patents being found invalid or unenforceable; costs and resources of operating as a public company; and unfavorable or no analyst research or reports.
These and other important factors discussed under the caption “Risk Factors” in our Quarterly Report on Form 10-Q for the period ended March 31, 2026, and our other reports filed with the U.S. Securities and Exchange Commission, could cause actual results to differ materially from those indicated by the forward-looking statements made in this press release. Any such forward-looking statements represent management's estimates as of the date of this press release. While we may elect to update such forward-looking statements at some point in the future, except as required by law, we disclaim any obligation to do so, even if subsequent events cause our views to change. These forward-looking statements should not be relied upon as representing our views as of any date subsequent to the date of this press release.
Global pivotal Phase 3 trial will evaluate efficacy and safety of atebimetinib + modified gemcitabine/nab-paclitaxel (mGnP) compared to standard GnP alone
Topline data readout, including primary endpoint of overall survival, anticipated in mid-2028
NEW YORK, June 11, 2026 (GLOBE NEWSWIRE) -- Immuneering Corporation (Nasdaq: IMRX), a late-stage clinical oncology company focused on keeping cancer patients alive and helping them thrive, today announced that the first patient has been dosed in MAPKeeper 301, a global, randomized, open-label pivotal Phase 3 clinical trial evaluating atebimetinib plus modified gemcitabine/nab-paclitaxel (mGnP) in first-line metastatic pancreatic cancer patients. Atebimetinib is a novel MEK inhibitor with a pulsatile mechanism designed to target RAS, RAF, and other MAPK pathway-driven cancers with greater durability and tolerability than traditional chronic inhibitors.
“Pancreatic cancer remains a challenging malignancy to treat,” said Eileen M. O’Reilly, MD, FASCO, Winthrop Rockefeller Endowed Chair in Medical Oncology at Memorial Sloan Kettering Cancer Center, and the lead principal investigator of the MAPKeeper 301 study. “There is an urgent need for new first-line treatment options that can improve treatment outcomes by augmenting survival and improving quality of life. The MAPKeeper 301 trial evaluating atebimetinib with standard of care therapy represents an exciting step toward addressing that need.”
The global MAPKeeper 301 trial (NCT07562152) is evaluating the safety and efficacy of atebimetinib + mGnP in patients with metastatic pancreatic ductal adenocarcinoma (PDAC) who have received no prior systemic anti-cancer therapy. Patients are being randomized to receive either atebimetinib + mGnP, or standard GnP treatment alone. The primary endpoint is overall survival (OS) of patients in the atebimetinib + mGnP arm versus patients in the GnP arm. Key secondary endpoints include progression free survival (PFS), overall response rate (ORR), disease control rate (DCR), safety and tolerability, and quality of life.
“The dosing of the first patient in our pivotal Phase 3 trial is a significant milestone for Immuneering and, more importantly, patients with pancreatic cancer and their families,” said Ben Zeskind, PhD, CEO of Immuneering. “Global interest in MAPKeeper-301 has been overwhelming, largely driven by our highly encouraging survival and tolerability data presented earlier this year. We look forward to initiating more sites and dosing more patients as expeditiously as possible with topline data from the pivotal trial expected in mid-2028.”
More information about the MAPKeeper 301 trial can be found at www.clinicaltrials.gov, identifier NCT07562152 or the MAPKeeper 301 clinical trial microsite at http://mapkeeper301.com/
About Pancreatic Ductal Adenocarcinoma (PDAC)
According to the National Health Institute, PDAC is the most common and highly lethal form of pancreatic cancer with nearly 68,000 new cases estimated for 2026 in the U.S. alone. Often diagnosed too late, PDAC currently carries a poor prognosis with a five-year survival rate of approximately 13%. Atebimetinib targets MEK in the MAPK pathway, from which 90% of PDAC cases grow and thrive, and is designed to shrink tumors durably with less resistance, optimize tolerability and counteract cachexia, enabling patients to live longer, stay strong and thrive.
About Immuneering
Immuneering is a late-stage clinical oncology company dedicated to keeping cancer patients alive and helping them thrive, with an initial focus on patients with RAS, RAF, and other MAPK-driven cancers. The Company is developing an entirely new category of cancer medicines, Deep Cyclic Inhibitors, designed to improve overall survival by three mechanisms: shrinking tumors durably with less resistance, preserving body mass by countering cachexia, and minimizing side effects to maximize performance status and combinability. Immuneering’s lead product candidate, atebimetinib, is an investigational, oral, once-daily Deep Cyclic Inhibitor of MEK, designed to improve survival across many cancer indications. The company is conducting a global randomized pivotal trial, MAPKeeper 301, evaluating atebimetinib in combination with chemotherapy in first-line pancreatic cancer patients. The Company’s development pipeline also includes additional combination opportunities and preclinical stage programs. For more information, please visit www.immuneering.com.
Forward-Looking Statements
This press release contains forward-looking statements, including within the meaning of the Private Securities Litigation Reform Act of 1995. All statements contained in this press release that do not relate to matters of historical fact should be considered forward-looking statements, including, without limitation, statements regarding: the treatment potential of atebimetinib, alone or in combination with other agents to treat cancer, including modified Gemcitabine/nab-paclitaxel (mGnP) in first-line pancreatic cancer and its potential to deliver overall survival with both durability and tolerability; the timing of the topline readout of MAPKeeper 301, the ability of the three design mechanisms of atebimetinib to shrink tumors durably, improve overall survival and overcome the limitations of conventional MAPK inhibition, including to impose less selective pressure, and provide a more sustained clinical benefit for patients.
These forward-looking statements are based on management’s current expectations. These statements are neither promises nor guarantees, but involve known and unknown risks, uncertainties and other important factors that may cause our actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements, including, but not limited to, the following: the risks inherent in oncology drug research and development, including target discovery, target validation, lead compound identification, and lead compound optimization; we have incurred significant losses, are not currently profitable and may never become profitable; our projected cash runway; our need for additional funding; our unproven approach to therapeutic intervention; our ability to address regulatory questions and the uncertainties relating to regulatory filings, reviews and approvals; the lengthy, expensive, and uncertain process of clinical drug development, including potential delays in activation of trial sites or enrollment of trial participants, or failure to obtain regulatory approvals; our reliance on third parties and collaborators to conduct our clinical trials, manufacture our product candidates, and develop and commercialize our product candidates, if approved; failure to compete successfully against other drug companies; protection of our proprietary technology and the confidentiality of our trade secrets; potential lawsuits for, or claims of, infringement of third-party intellectual property or challenges to the ownership of our intellectual property; our patents being found invalid or unenforceable; costs and resources of operating as a public company; and unfavorable or no analyst research or reports.
These and other important factors discussed under the caption “Risk Factors” in our Quarterly Report on Form 10-Q for the period ended March 31, 2026, and our other reports filed with the U.S. Securities and Exchange Commission, could cause actual results to differ materially from those indicated by the forward-looking statements made in this press release. Any such forward-looking statements represent management's estimates as of the date of this press release. While we may elect to update such forward-looking statements at some point in the future, except as required by law, we disclaim any obligation to do so, even if subsequent events cause our views to change. These forward-looking statements should not be relied upon as representing our views as of any date subsequent to the date of this press release.
, /CNW/ - BMO Financial Group (TSX: BMO) (NYSE: BMO) will host an all-bank Investor Day in Toronto on Thursday, March 26, 2026. The event will feature presentations from Darryl White, Chief Executive Officer, and members of BMO's senior executive leadership team.
Registration details, agenda and speaker information can be found at https://www.bmo.com/main/about-bmo/investor-relations/presentations-events. The live webcast and presentation slides will be posted on the day of the event.
About BMO Financial Group
BMO Financial Group is the eighth largest bank in North America by assets, with total assets of $1.5 trillion as of January 31, 2026. Serving customers for 200 years and counting, BMO is a diverse team of highly engaged employees providing a broad range of personal and commercial banking, wealth management, global markets and investment banking products and services to approximately 13 million customers across Canada, the United States, and in select markets globally. Driven by a single purpose, to Boldly Grow the Good in business and life, BMO is committed to driving positive change in the world, and making progress for a thriving economy, sustainable future, and stronger communities.
Supports BMO's strategy to elevate returns and accelerate growth; transaction accretive to capital ratios and ROE Positions these premier businesses for continued growth in an efficient capital structure BMO to invest in a 19.9% equity interest, enabling continued participation in the businesses' long-term value creation , /CNW/ - BMO Financial Group (TSX: BMO) (NYSE: BMO) today announced the signing of a definitive agreement with Stonepeak for the sale of BMO's Transportation Finance and Vendor Finance businesses, including related loan portfolios in the United States and Canada.
The transaction will advance BMO's strategic priorities by improving capital efficiency and sharpening its focus on core markets where the bank has deep client relationships and attractive long-term growth opportunities.
"This transaction is consistent with BMO's focus on delivering sustained profitable growth, and enables us to invest in areas that deliver the full power of BMO to our clients," said Aron Levine, President, BMO U.S. "We're allocating capital to areas with strong potential for long-term value creation while obtaining an equity interest in future income of the transportation and vendor finance businesses through a more capital efficient structure. Following the transition, Stonepeak will continue to provide best-in-class client experiences, supported by its strong global infrastructure platform and deep expertise in transportation-focused asset leasing."
BMO's Transportation Finance business provides specialized financing for trucks and trailers predominantly through dealer-managed relationships, and its Vendor Finance business offers equipment financing through original equipment manufacturers and their dealer networks. The combined loan and lease portfolio in the United States and Canada totals approximately C$14.5 billion as of March 31, 2026.
Headquartered in New York, Stonepeak is a leading alternative investment firm specializing in infrastructure and real assets with approximately US$88 billion of assets under management. Stonepeak's target sectors include transportation and logistics, digital infrastructure, energy and energy transition, and real estate.
"Building on decades of sector expertise, BMO Transportation and Vendor Finance has established itself as one of North America's premier transportation financing platforms," said Will Schleier, Senior Managing Director at Stonepeak. "We are excited to work closely with BMO and the outstanding leadership team in place to invest further in the business, build on its strong performance, and grow its commercial customer base while preserving the culture, reputation, and relationships that have made the business so successful to date."
Transaction Highlights
Under the terms of the agreement, Stonepeak will acquire the assets of BMO's Transportation Finance and Vendor Finance businesses for cash consideration and an earnout contingent upon the business achieving specified future performance targets. BMO will use a portion of the consideration to invest an approximate 19.9% equity interest in the new entity.
For accounting purposes, the businesses will be classified as held for sale, and BMO expects to record a net after-tax charge of approximately C$0.9 billion primarily related to goodwill in the third quarter of 2026, which will be reported in the Corporate Services segment and treated as an adjusting item. This amount is subject to closing adjustments and foreign exchange rates prevailing at the date of closing.
Transaction aligns with BMO's strategy to elevate returns
On a pro forma basis, the transaction is expected to improve the bank's common equity Tier 1 (CET1) ratio by approximately 28 bps primarily from the reduction in risk weighted assets and be accretive to the bank's return on equity. The transaction is not expected to have a significant impact on the bank's future run rate earnings.
The transaction is expected to close in the fourth quarter of fiscal 2026, subject to regulatory approvals and customary closing conditions. BMO and Stonepeak will work together to ensure a smooth transition.
For additional information about this transaction please refer to the BMO Investor Relations website at www.bmo.com/main/about-bmo/investor-relations/acquisitions
In connection with the transaction, BMO Capital Markets and BofA Securities acted as BMO's financial advisors. Sullivan & Cromwell LLP and Osler, Hoskin & Harcourt LLP acted as legal counsel to BMO. Skadden, Arps, Slate, Meagher & Flom LLP and Blake, Cassels & Graydon LLP acted as legal counsel to Stonepeak.
About BMO Financial Group
BMO Financial Group is the eighth largest bank in North America by assets, with total assets of $1.5 trillion as of January 31, 2026. Serving clients for 200 years and counting, BMO is a diverse team of highly engaged employees providing a broad range of personal and commercial banking, wealth management, global markets and investment banking products and services to approximately 13 million clients across Canada, the United States, and in select markets globally. Driven by a single purpose, to Boldly Grow the Good in business and life, BMO is committed to driving positive change in the world, and making progress for a thriving economy, sustainable future, and stronger communities.
About Stonepeak
Stonepeak is a leading alternative investment firm specializing in infrastructure and real assets with approximately $88 billion of assets under management. Through its investment in defensive, hard-asset businesses globally, Stonepeak aims to create value for its investors and portfolio companies, with a focus on downside protection and strong risk-adjusted returns. Stonepeak, as sponsor of private equity and credit investment vehicles, provides capital, operational support, and committed partnership to grow investments in its target sectors, which include digital infrastructure, energy and energy transition, transport and logistics, and real estate. Stonepeak is headquartered in New York with offices in Houston, Washington, D.C., London, Hong Kong, Seoul, Singapore, Sydney, Tokyo, Abu Dhabi, and Riyadh. For more information, please visit www.stonepeak.com.
Caution Regarding Forward Looking Statements
Certain statements in this press release are forward-looking statements. All such statements are made pursuant to the "safe harbor" provisions of, and are intended to be forward-looking statements under, the United States Private Securities Litigation Reform Act of 1995 and any applicable Canadian securities legislation. These forward-looking statements include, but are not limited to, statements with respect to the expected closing of the proposed transaction, the potential payment of an earn-out, the financial, operational and capital impact of the proposed transaction, the future performance of the transportation and vendor finance businesses, our strategies or future actions, our targets and commitments, expectations for our financial condition and capital position, and include statements made by our management. Forward-looking statements are typically identified by words such as "expect", "anticipate", "will", "may" or negative or grammatical variations thereof.
By their nature, forward-looking statements are based on various assumptions and are subject to inherent risks and uncertainties. We caution readers of this press release not to place undue reliance on our forward-looking statements as the assumptions underlying such statements may not turn out to be correct and a number of factors could cause actual future results, conditions, actions or events to differ materially from the targets, expectations, estimates or intentions expressed in the forward-looking statements. Such factors include, but are not limited to: the possibility that the proposed transaction does not close when expected or at all because required regulatory approvals and other conditions to closing are not received or satisfied on a timely basis or at all or are received subject to adverse conditions or requirements; the anticipated benefits from the proposed transaction, such as it being accretive to BMO's return on equity, improving BMO's common equity Tier 1 capital ratio (CET 1 ratio) and receiving a payment in respect of the earnout, are not realized in the time frame anticipated or at all as a result of the performance of the transportation and vendor finance businesses, changes in general economic and market conditions, interest and exchange rates, monetary policy, laws and regulations (including changes to capital requirements) and their enforcement; reputational risks and the reaction of BMO's customers and employees to the transaction; diversion of management time on transaction-related issues; and those other factors discussed in the Risks That May Affect Future Results section, and the sections related to credit and counterparty, market, liquidity and funding, operational non-financial, legal and regulatory compliance, strategic, environmental and social, and reputation risk, in the Enterprise-Wide Risk Management section of BMO's 2025 Annual Report, and the Risk Management section in BMO's First Quarter 2026 Report to Shareholders, all of which outline certain key factors and risks that may affect our future results and our ability to anticipate and effectively manage risks arising from all of the foregoing factors.. We caution that the foregoing list is not exhaustive of all possible factors. These factors should be considered in addition to other uncertainties and potential events, and the inherent uncertainty of forward-looking statements.
Assumptions about BMO expected financial performance (including balance sheet, income statement and regulatory capital figures), expected closing date of the proposed transaction, restructuring costs, and assumed accounting treatment were considered in estimating the impact of the transaction on BMO's return on equity and CET1 ratio.
BMO does not undertake to update any forward-looking statement, whether written or oral, that may be made, from time to time, by the organization or on its behalf, except as required by law.
BMO's Second Quarter 2026 Report to Shareholders, including the unaudited interim consolidated financial statements for the period ended April 30, 2026, are available online at www.bmo.com/investorrelations, on the Canadian Securities Administrators' website at www.sedarplus.ca, and on the EDGAR section of the U.S. Securities and Exchange Commission's website at www.sec.gov.
Financial Results Highlights
Second Quarter 2026 compared with Second Quarter 2025:
Reported net income1 of $2,630 million, an increase of 34% from $1,962 million; adjusted net income1 of $2,733 million, an increase of 34% from $2,046 million Reported earnings per share (EPS)2 of $3.53, an increase of 41% from $2.50; adjusted EPS1, 2 of $3.67, an increase of 40% from $2.62 Provision for credit losses (PCL) of $739 million, a decrease from $1,054 million Reported return on equity (ROE) of 13.0%, compared with 9.4%; adjusted ROE1 of 13.5%, compared with 9.8% Common Equity Tier 1 (CET1) Ratio3 of 13.0%, compared with 13.5% Declared a quarterly dividend of $1.71 per common share, an increase of $0.08 or 5% from the prior year and $0.04 or 2% from the prior quarter Year-to-Date 2026 compared with Year-to-Date 2025:
Reported net income1 of $5,119 million, an increase of 25% from $4,100 million; adjusted net income1 of $5,284 million, an increase of 22% from $4,335 million Reported EPS2 of $6.92, an increase of 30% from $5.34; adjusted EPS1, 2 of $7.15, an increase of 26% from $5.66 PCL of $1,485 million, a decrease from $2,065 million Reported ROE of 12.5%, compared with 10.0%; adjusted ROE1 of 12.9%, compared with 10.6% , /CNW/ - BMO Financial Group (TSX:BMO) (NYSE:BMO) reported net income for the second quarter ended April 30, 2026 was $2,630 million, compared with $1,962 million in the prior year, and EPS of $3.53, compared with $2.50. Reported ROE was 13.0%, compared with 9.4% in the prior year. Adjusted net income was $2,733 million and adjusted EPS was $3.67, an increase from $2,046 million and $2.62, respectively, in the prior year. Adjusted ROE was 13.5%, compared with 9.8% in the prior year.
"At our March Investor Day, we reviewed our plan to elevate returns and accelerate growth. Our second quarter results continued to demonstrate meaningful progress and momentum against these commitments. We once again strengthened ROE and delivered strong EPS growth, driven by robust fee revenue across Capital Markets, Wealth Management and Treasury and Payments. We delivered solid sequential commercial banking loan growth in both Canada and the United States, reflecting improving client activity and the strength of our bankers. These outcomes are driven by our focus on deepening client relationships, innovating to drive business value, and optimizing performance," said Darryl White, CEO of BMO Financial Group.
"Our value‑driven approach to human‑ and AI‑powered client experiences is delivering tangible benefits. To continue to advance our innovation strategy, we recently established the BMO Institute for Applied Artificial Intelligence & Quantum, dedicated to the responsible application, governance and oversight of AI at scale, and support our clients as they integrate AI into their companies and households. Disciplined investment, capital and risk management continue to strengthen our earnings quality, creating sustainable long‑term value for our shareholders," concluded Mr. White.
Concurrent with the release of results, BMO announced a third quarter 2026 dividend of $1.71 per common share, an increase of $0.04 or 2% from the prior quarter and an increase of $0.08 or 5% from the prior year. The quarterly dividend of $1.71 is equivalent to an annual dividend of $6.84 per common share. During the quarter, we purchased for cancellation 6.0 million common shares under the normal course issuer bid, at an average price of $193.47 per share.
On May 11, 2026, we entered into a definitive agreement with Stonepeak for the sale of BMO's Transportation Finance and Vendor Finance businesses, including related loan portfolios which are part of our U.S. Banking and Canadian P&C operating segments. Stonepeak will acquire the assets of these businesses for cash consideration and an earn-out contingent upon the business achieving specified future performance targets. BMO will use a portion of the consideration to invest an approximate 19.9% equity interest in the new entity.
The transaction met the accounting requirements for assets held for sale in the third quarter of fiscal 2026, and as a result, we expect to recognize a charge of approximately $1.1 billion pre-tax ($0.9 billion after-tax), primarily related to goodwill recorded in Corporate Services and treated as an adjusting item. The final amount is subject to closing adjustments and foreign exchange rates prevailing at the date of closing. This transaction is expected to close in the fourth quarter of fiscal 2026, subject to regulatory approvals and customary closing conditions.
Caution
The foregoing section contains forward-looking statements. Please refer to the Caution Regarding Forward-Looking Statements section.
(1)
Results and measures in this document are presented on a generally accepted accounting principles (GAAP) basis. They are also presented on an adjusted basis that excludes the impact of certain specified items from reported results. Adjusted results and ratios are non-GAAP and are detailed in the Non-GAAP and Other Financial Measures section. Unless otherwise indicated, all amounts are in Canadian dollars. All ratios and percentage changes in this document are based on unrounded numbers.
(2)
All EPS measures in this document refer to diluted EPS, unless specified otherwise.
(3)
The CET1 Ratio is disclosed in accordance with the Capital Adequacy Requirements (CAR) Guideline, as set out by the Office of the Superintendent of Financial Institutions (OSFI), as applicable.
Second Quarter 2026 Performance Review
Adjusted results and ratios in this section are on a non-GAAP basis. Refer to the Non-GAAP and Other Financial Measures section for further information on adjusting items.
Canadian P&C
Reported net income was $884 million, an increase of $120 million or 15% from the prior year, and adjusted net income was $887 million, an increase of $119 million or 15%, primarily due to a 5% increase in revenue, as well as a lower provision for credit losses, partially offset by higher expenses. Revenue growth was driven by increases in net interest income, primarily due to higher net interest margin, and non-interest revenue due to higher card-related and mutual fund distribution fees, partially offset by lower deposit fee revenue.
U.S. Banking
Reported net income was $790 million, an increase of $189 million or 32% from the prior year, and adjusted net income was $847 million, an increase of $172 million or 25%. The impact of the weaker U.S. dollar decreased net income by 5%, revenue by 4% and expenses by 3%.
On a U.S. dollar basis, reported net income was $575 million, an increase of $154 million or 37% from the prior year, and adjusted net income was $616 million, an increase of $143 million or 30%, primarily due to a 5% increase in revenue and a lower provision for credit losses, with expenses relatively unchanged from the prior year. Revenue growth was driven by higher non-interest revenue, including the impact of a loss on the sale of a non-relationship U.S. credit card portfolio in the prior year, and higher net interest income due to higher net interest margin, partially offset by lower balances.
Wealth Management
Reported net income was $428 million, an increase of $108 million or 34% from the prior year, and adjusted net income was $444 million, an increase of $124 million or 39%. Wealth and Asset Management reported net income was $342 million, an increase of $81 million or 31%, and adjusted net income was $358 million, an increase of $97 million or 37%, reflecting higher revenue, primarily due to the impact of stronger global markets and net sales, higher net interest income, as well as the inclusion of Burgundy Asset Management (Burgundy), partially offset by higher expenses. Insurance net income was $86 million, an increase of $27 million or 47% from the prior year, primarily due to favourable market movements in the current year.
Capital Markets
Reported net income was $638 million, an increase of $204 million or 47% from the prior year, and adjusted net income was $641 million, an increase of $204 million or 46%, reflecting higher revenue in Global Markets and Investment and Corporate Banking, and a lower provision for credit losses, partially offset by higher expenses.
Corporate Services
Reported net loss was $110 million, compared with a reported net loss of $157 million in the prior year, and adjusted net loss was $86 million, compared with an adjusted net loss of $154 million, with changes driven by higher treasury-related revenue.
Credit Quality
Total provision for credit losses was $739 million, compared with a provision of $1,054 million in the prior year. The provision for credit losses on impaired loans was $734 million, a decrease of $31 million, primarily due to lower provisions in Capital Markets and U.S. Banking. The provision for credit losses on performing loans was $5 million, compared with $289 million in the prior year. The performing provision in the current quarter was primarily driven by the net impact of model changes, largely offset by portfolio credit migration and lower portfolio balances, while the prior year reflected changes in the macroeconomic environment.
Refer to the Critical Accounting Estimates and Judgments section of BMO's 2025 Annual Report and Note 3 of the audited annual consolidated financial statements for further information on the allowance for credit losses as at October 31, 2025.
Capital
BMO's Common Equity Tier 1 (CET1) Ratio was 13.0% as at April 30, 2026, a decrease from 13.1% at the end of the first quarter of 2026, as internal capital generation was more than offset by the impact of the purchase of common shares for cancellation and higher source currency risk-weighted assets.
Non-GAAP and Other Financial Measures
Results and measures in this document are presented on a generally accepted accounting principles (GAAP) basis. Unless otherwise indicated, all amounts are in Canadian dollars and have been derived from our audited annual consolidated financial statements and our unaudited interim consolidated financial statements, prepared in accordance with International Financial Reporting Standards (IFRS), as issued by the International Accounting Standards Board (IASB). References to GAAP mean IFRS. We use a number of financial measures to assess our performance, as well as the performance of our operating segments, including amounts, measures and ratios that are presented on a non‑GAAP basis, as described below. We believe that these non‑GAAP amounts, measures and ratios, read together with our GAAP results, provide readers with a better understanding of how management assesses results.
Non-GAAP amounts, measures and ratios do not have standardized meanings under GAAP. They are unlikely to be comparable to similar measures presented by other companies and should not be viewed in isolation from, or as a substitute for, GAAP results.
Certain information contained in BMO's Second Quarter 2026 Management's Discussion and Analysis dated May 27, 2026, for the period ended April 30, 2026, is incorporated by reference into this document. For further details on the composition of our supplementary financial measures, refer to the Glossary of Financial Terms section of BMO's Second Quarter 2026 Report to Shareholders, which is available online at www.bmo.com/investorrelations and at www.sedarplus.ca.
Adjusted measures and ratios
Management considers both reported and adjusted results and measures to be useful in assessing underlying ongoing business performance. Adjusted results and measures remove certain specified items from revenue, non‑interest expense and income taxes, as detailed in the following table. Adjusted results and measures presented in this document are non‑GAAP. Presenting results on both a reported and an adjusted basis permits readers to assess the impact of certain items on results for the periods presented, and to better assess results excluding those items that may not reflect ongoing business performance. As such, the presentation may facilitate readers' analysis of underlying trends. Except as otherwise noted, management's discussion of changes in reported results in this document applies equally to changes in the corresponding adjusted results.
Net Interest Margin, excluding Global Markets and Insurance
Effective the first quarter of fiscal 2026, we report net interest margin on a basis that excludes net interest income from our Global Markets business in Capital Markets, and average earning assets from our Global Markets and Insurance businesses. Management considers this measure to be useful in allowing readers to assess performance of BMO's lending, investing and deposit-raising activities without the volatility that may be associated with market and trading-related activities. This measure replaces net interest margin, excluding trading and insurance previously disclosed, and prior periods have been reclassified to conform with the current period's presentation.
Tangible common equity and return on tangible common equity
Tangible common equity is calculated as common shareholders' equity, less goodwill and acquisition-related intangible assets, net of related deferred tax liabilities. Return on tangible common equity (ROTCE) is calculated as net income available to common shareholders, adjusted for the amortization of acquisition-related intangible assets and any impairments, as a percentage of average tangible common equity. ROTCE is commonly used in the North American banking industry and is meaningful as a consistent measure of the performance of businesses, whether they were acquired or developed organically.
Adjusting Items
Adjusted results in the current quarter and prior periods excluded the following items:
Impact of divestitures related to the announced sale of 138 branches in select U.S. markets, recorded in non-interest expense in Corporate Services. Q2-2026 included expenses of $26 million ($24 million after-tax), comprising a write-down of goodwill of $18 million and divestiture-related costs of $8 million. Prior periods included divestiture-related costs of $4 million ($3 million after-tax) in Q1-2026. Acquisition and integration costs of $3 million ($2 million after-tax) in the current quarter. Prior periods included expenses of $9 million ($7 million after-tax) in Q1-2026, a reversal of $2 million ($1 million after-tax) in Q2-2025 and expenses of $10 million ($7 million after-tax) in Q1-2025. Amounts are recorded in non-interest expense in the related operating segment: Burgundy in Wealth Management and Bank of the West in Corporate Services. Amortization of acquisition-related intangible assets of $93 million ($70 million after-tax) in the current quarter. Prior periods included $96 million ($71 million after-tax) in Q1-2026, $109 million ($81 million after-tax) in Q2-2025 and $106 million ($79 million after-tax) in Q1-2025. Amounts are recorded in non-interest expense in the related operating segment. Change in the fair value of contingent consideration related to the acquisition of Burgundy, which reduced non-interest revenue in the current quarter by $7 million (pre-tax and after-tax), recorded in Wealth Management. Q1-2026 included a reduction of $16 million (pre-tax and after-tax). For further information, refer to Note 13 of the unaudited interim consolidated financial statements and Note 9 of the audited annual consolidated financial statements of BMO's 2025 Annual Report. U.S. Federal Deposit Insurance Corporation (FDIC) special assessment recorded in non-interest expense in Corporate Services. Q1-2026 included a partial reversal of a prior charge of $47 million ($35 million after-tax). Prior periods included expenses of $5 million ($4 million after-tax) in Q2-2025 and a partial reversal of $7 million ($5 million after-tax) in Q1-2025. Impact of aligning accounting policies for employee vacation across legal entities of $96 million ($70 million after-tax) in Q1-2025, recorded in non-interest expense in Corporate Services. Adjusting items in aggregate decreased net income by $103 million in the current quarter, compared with a $84 million decrease in the prior year and a decrease of $62 million in the prior quarter. On a year-to-date basis, adjusting items in aggregate decreased net income by $165 million, compared with a decrease of $235 million in the prior year.
Non-GAAP and Other Financial Measures (1)
TABLE 1
(Canadian $ in millions, except as noted)
Q2-2026
Q1-2026
Q2-2025
YTD-2026
YTD-2025
Reported Results
Net interest income
5,268
5,643
5,097
10,911
10,495
Non-interest revenue
4,299
4,181
3,582
8,480
7,450
Revenue
9,567
9,824
8,679
19,391
17,945
Provision for credit losses
739
746
1,054
1,485
2,065
Non-interest expense
5,330
5,753
5,019
11,083
10,446
Income before income taxes
3,498
3,325
2,606
6,823
5,434
Provision for income taxes
868
836
644
1,704
1,334
Net income
2,630
2,489
1,962
5,119
4,100
Dividends on preferred shares and distributions on other equity instruments
139
81
142
220
207
Net income (loss) attributable to non-controlling interest in subsidiaries
4
(1)
2
3
6
Net income available to common shareholders
2,487
2,409
1,818
4,896
3,887
Diluted EPS ($)
3.53
3.39
2.50
6.92
5.34
Adjusting Items Impacting Revenue (Pre-tax)
Change in fair value of contingent consideration (2)
Amortization of acquisition-related intangible assets (3)
(70)
(71)
(81)
(141)
(160)
Impact of divestitures
(24)
(3)
–
(27)
–
FDIC special assessment
–
35
(4)
35
1
Impact of alignment of accounting policies
–
–
–
–
(70)
Impact of adjusting items on non-interest expense (after-tax)
(96)
(46)
(84)
(142)
(235)
Impact of adjusting items on reported net income (after-tax)
(103)
(62)
(84)
(165)
(235)
Impact on diluted EPS ($)
(0.14)
(0.09)
(0.12)
(0.23)
(0.32)
Adjusted Results
Net interest income
5,268
5,643
5,097
10,911
10,495
Non-interest revenue
4,306
4,197
3,582
8,503
7,450
Revenue
9,574
9,840
8,679
19,414
17,945
Provision for credit losses
739
746
1,054
1,485
2,065
Non-interest expense
5,208
5,691
4,907
10,899
10,129
Income before income taxes
3,627
3,403
2,718
7,030
5,751
Provision for income taxes
894
852
672
1,746
1,416
Net income
2,733
2,551
2,046
5,284
4,335
Net income available to common shareholders
2,590
2,471
1,902
5,061
4,122
Diluted EPS ($)
3.67
3.48
2.62
7.15
5.66
(1)
Adjusted results exclude certain items from reported results and are used to calculate our adjusted measures as presented in the table above. Refer to the commentary in this Non-GAAP and Other Financial Measures section for further information on adjusting items.
(2)
Recorded in non-interest revenue.
(3)
Represents amortization of acquisition-related intangible assets and any impairment.
Summary of Reported and Adjusted Results by Operating Segment
TABLE 2
Wealth
Capital
Corporate
U.S. Operations (1)
(Canadian $ in millions, except as noted)
Canadian P&C
U.S. Banking
Management
Markets
Services
Total Bank
(US$ in millions)
Q2-2026
Reported net income (loss)
884
790
428
638
(110)
2,630
655
Dividends on preferred shares and distributions on
other equity instruments
11
14
1
15
98
139
15
Net income attributable to non-controlling interest in subsidiaries
–
4
–
–
–
4
3
Net income (loss) available to common shareholders
873
772
427
623
(208)
2,487
637
Acquisition and integration costs
–
–
2
–
–
2
–
Amortization of acquisition-related intangible assets
3
57
7
3
–
70
43
Change in fair value of contingent consideration
–
–
7
–
–
7
–
Impact of divestitures
–
–
–
–
24
24
18
Adjusted net income (loss) (2)
887
847
444
641
(86)
2,733
716
Adjusted net income (loss) available to common shareholders (2)
876
829
443
626
(184)
2,590
698
Q1-2026
Reported net income (loss)
948
742
352
657
(210)
2,489
715
Dividends on preferred shares and distributions on
other equity instruments
13
14
2
15
37
81
17
Net income (loss) attributable to non-controlling interest in subsidiaries
–
(2)
–
–
1
(1)
(1)
Net income (loss) available to common shareholders
935
730
350
642
(248)
2,409
699
Acquisition and integration costs
–
–
7
–
–
7
–
Amortization of acquisition-related intangible assets
3
60
5
3
–
71
46
Change in fair value of contingent consideration
–
–
16
–
–
16
–
Impact of divestitures
–
–
–
–
3
3
2
FDIC special assessment
–
–
–
–
(35)
(35)
(26)
Adjusted net income (loss) (2)
951
802
380
660
(242)
2,551
737
Adjusted net income (loss) available to common shareholders (2)
938
790
378
645
(280)
2,471
721
Q2-2025
Reported net income (loss)
764
601
320
434
(157)
1,962
515
Dividends on preferred shares and distributions on
other equity instruments
11
16
1
10
104
142
3
Net income (loss) attributable to non-controlling interest in subsidiaries
–
5
–
–
(3)
2
1
Net income (loss) available to common shareholders
753
580
319
424
(258)
1,818
511
Acquisition and integration costs/reversal
–
–
–
–
(1)
(1)
(1)
Amortization of acquisition-related intangible assets
4
74
–
3
–
81
54
FDIC special assessment
–
–
–
–
4
4
3
Adjusted net income (loss) (2)
768
675
320
437
(154)
2,046
571
Adjusted net income (loss) available to common shareholders (2)
757
654
319
427
(255)
1,902
567
YTD-2026
Reported net income (loss)
1,832
1,532
780
1,295
(320)
5,119
1,370
Dividends on preferred shares and distributions on
other equity instruments
24
28
3
30
135
220
32
Net income attributable to non-controlling interest in subsidiaries
–
2
–
–
1
3
2
Net income (loss) available to common shareholders
1,808
1,502
777
1,265
(456)
4,896
1,336
Acquisition and integration costs
–
–
9
–
–
9
–
Amortization of acquisition-related intangible assets
6
117
12
6
–
141
89
Change in fair value of contingent consideration
–
–
23
–
–
23
–
Impact of divestitures
–
–
–
–
27
27
20
FDIC special assessment
–
–
–
–
(35)
(35)
(26)
Adjusted net income (loss) (2)
1,838
1,649
824
1,301
(328)
5,284
1,453
Adjusted net income (loss) available to common shareholders (2)
1,814
1,619
821
1,271
(464)
5,061
1,419
(1)
U.S. Operations comprises reported and adjusted results recorded in U.S. Banking, and the U.S. operations in Capital Markets and Corporate Services.
(2)
Refer to the commentary in this Non-GAAP and Other Financial Measures section for details on adjusting items.
Certain comparative figures have been reclassified to conform with the current period's presentation.
Summary of Reported and Adjusted Results by Operating Segment (Continued)
TABLE 2 (Continued)
Wealth
Capital
Corporate
U.S. Operations (1)
(Canadian $ in millions, except as noted)
Canadian P&C
U.S. Banking
Management
Markets
Services
Total Bank
(US$ in millions)
YTD-2025
Reported net income (loss)
1,641
1,236
648
1,023
(448)
4,100
1,154
Dividends on preferred shares and distributions on
other equity instruments
23
31
3
20
130
207
6
Net income attributable to non-controlling interest in subsidiaries
–
5
–
–
1
6
4
Net income (loss) available to common shareholders
1,618
1,200
645
1,003
(579)
3,887
1,144
Acquisition and integration costs
–
–
–
–
6
6
4
Amortization of acquisition-related intangible assets
7
146
–
7
–
160
106
FDIC special assessment
–
–
–
–
(1)
(1)
(1)
Impact of alignment of accounting policies
–
–
–
–
70
70
25
Adjusted net income (loss) (2)
1,648
1,382
648
1,030
(373)
4,335
1,288
Adjusted net income (loss) available to common shareholders (2)
1,625
1,346
645
1,010
(504)
4,122
1,278
See previous page for footnote references.
Certain comparative figures have been reclassified to conform with the current period's presentation.
Caution
This Non-GAAP and Other Financial Measures section contains forward-looking statements. Please refer to the Caution Regarding Forward-Looking Statements.
Caution Regarding Forward-Looking Statements
Bank of Montreal's public communications often include written or oral forward-looking statements. Statements of this type are included in this document and may be included in other filings with Canadian securities regulators or the U.S. Securities and Exchange Commission, or in other communications. All such statements are made pursuant to the "safe harbor" provisions of, and are intended to be forward-looking statements under, the United States Private Securities Litigation Reform Act of 1995 and any applicable Canadian securities legislation. Forward-looking statements in this document may include, but are not limited to: statements with respect to our objectives and priorities for fiscal 2026 and beyond; our strategies or future actions; our targets and commitments; expectations for our financial condition, capital position, the regulatory environment in which we operate, the results of, or outlook for, our operations or the Canadian, U.S. and international economies; and include statements made by our management. Forward-looking statements are typically identified by words such as "will", "would", "should", "believe", "expect", "anticipate", "project", "intend", "estimate", "plan", "goal", "commit", "target", "may", "might", "schedule", "forecast", "outlook", "timeline", "suggest", "seek" and "could" or negative or grammatical variations thereof.
By their nature, forward-looking statements require us to make assumptions and are subject to inherent risks and uncertainties, both general and specific in nature. There is significant risk that predictions, forecasts, conclusions or projections will not prove to be accurate, that our assumptions may not be correct, and that actual results may differ materially from such predictions, forecasts, conclusions or projections. We caution readers of this document not to place undue reliance on our forward-looking statements, as a number of factors – many of which are beyond our control and the effects of which can be difficult to predict – could cause actual future results, conditions, actions or events to differ materially from the targets, expectations, estimates or intentions expressed in the forward-looking statements.
The future outcomes that relate to forward-looking statements may be influenced by many factors, including, but not limited to: general economic and market conditions in the countries in which we operate, including labour challenges and changes in foreign exchange and interest rates; political conditions, including changes relating to, or affecting, economic or trade matters, including tariffs, countermeasures and tariff mitigation policies; changes to our credit ratings; cyber and information security, including the threat of data breaches, hacking, identity theft and corporate espionage, as well as the possibility of denial of service resulting from efforts targeted at causing system failure and service disruption; technology resilience, innovation and competition; technological change, including the use of data and artificial intelligence (AI) in our business, including generative AI; failure of third parties to comply with their obligations to us; disruptions of global supply chains; environmental and social risk, including climate change; the Canadian housing market and consumer leverage; inflationary pressures; changes in laws, including tax legislation and interpretation, or in supervisory expectations or requirements, including capital, interest rate and liquidity requirements and guidance, including if the bank were designated a global systemically important bank, and the effect of such changes on funding costs and capital requirements; changes in monetary, fiscal or economic policy; weak, volatile or illiquid capital or credit markets; the level of competition in the geographic and business areas in which we operate; exposure to, and the resolution of, significant litigation or regulatory matters, our ability to successfully appeal adverse outcomes of such matters and the timing, determination and recovery of amounts related to such matters; the accuracy and completeness of the information we obtain with respect to our customers and counterparties; our ability to successfully execute our strategic plans, complete acquisitions or dispositions and integrate acquisitions, including obtaining regulatory approvals, and realize any anticipated benefits from such plans and transactions; critical accounting estimates and judgments, and the effects of changes in accounting standards, rules and interpretations on these estimates; operational and infrastructure risks, including with respect to reliance on third parties; global capital markets activities; the emergence or continuation of widespread health emergencies or pandemics, and their impact on local, national or international economies, as well as their heightening of certain risks that may affect our future results; the possible effects on our business of war or terrorist activities; natural disasters, such as earthquakes or flooding, and disruptions to public infrastructure, such as transportation, communications, power or water supply; and our ability to anticipate and effectively manage risks arising from all of the foregoing factors.
We caution that the foregoing list is not exhaustive of all possible factors. Other factors and risks could adversely affect our results. For further information, please refer to the discussion in the Risks That May Affect Future Results section, and the sections related to credit and counterparty, market, liquidity and funding, operational non-financial, legal and regulatory compliance, strategic, environmental and social, and reputation risk in the Enterprise-Wide Risk Management section of BMO's 2025 Annual Report, and the Risk Management section in our Second Quarter 2026 Report to Shareholders, all of which outline certain key factors and risks that may affect our future results. Investors and others should carefully consider these factors and risks, as well as other uncertainties and potential events, and the inherent uncertainty of forward-looking statements. We do not undertake to update any forward-looking statements, whether written or oral, that may be made from time to time by the organization or on its behalf, except as required by law. The forward-looking information contained in this document is presented for the purpose of assisting shareholders and analysts in understanding our financial position as at and for the periods ended on the dates presented, as well as our strategic priorities and objectives, and may not be appropriate for other purposes.
Material economic assumptions underlying the forward-looking statements contained in this document include those set out in the Economic Developments and Outlook section of BMO's 2025 Annual Report, as updated in the Economic Developments and Outlook section and the Risk Management – Geopolitical Developments section in our Second Quarter 2026 Report to Shareholders, as well as in the Allowance for Credit Losses section of BMO's 2025 Annual Report, as updated in the Allowance for Credit Losses section in our Second Quarter 2026 Report to Shareholders. Assumptions about the performance of the Canadian and U.S. economies, as well as overall market conditions and their combined effect on our business, are material factors we consider when determining our strategic priorities, objectives and expectations for our business. In determining our expectations for economic growth, we primarily consider historical economic data, past relationships between economic and financial variables, changes in government policies, and the risks to the domestic and global economy.
Investor and Media Information
Investor Presentation Materials
Interested parties are invited to visit BMO's website at www.bmo.com/investorrelations to review the 2025 Annual MD&A and audited annual consolidated financial statements, quarterly presentation materials and supplementary financial and regulatory information package.
Quarterly Conference Call and Webcast Presentations
Interested parties are also invited to listen to our quarterly conference call on Wednesday, May 27, 2026, at 8:15 a.m. (ET). The call may be accessed by telephone at 647-557-5533 (from within Toronto) or 1-888-440-4121 (toll-free outside Toronto), entering Passcode: 89709#. A replay of the conference call can be accessed until June 27, 2026, by calling 647-362-9199 (from within Toronto) or 1-800-770-2030 (toll-free outside Toronto) and entering Passcode: 89709#.
A live webcast of the call can be accessed on our website at www.bmo.com/investorrelations. A replay can also be accessed on the website.
Upcoming Events
Q3-2026 Earnings Release August 25, 2026 Q4-2026 Earnings Release December 2, 2026
Shareholder Dividend Reinvestment and Share Purchase Plan (DRIP)
Common shareholders may elect to have their cash dividends reinvested in
common shares of the bank, in accordance with the bank's DRIP. More
information about the Plan and how to enrol can be found at
www.bmo.com/investorrelations.
For dividend information, change in shareholder address
or to advise of duplicate mailings, please contact
Computershare Trust Company of Canada
320 Bay Street, 14th Floor
Toronto, Ontario M5H 4A6
Telephone: 416-263-9200
Fax: 1-888-453-0330
E-mail: [email protected]
For other shareholder information, please contact
Bank of Montreal
Shareholder Services
Corporate Secretary's Department
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Toronto, Ontario M5X 1A1
Telephone: 416-867-6785
E-mail: [email protected]
For further information on this document, please contact
Bank of Montreal
Investor Relations Department
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BMO's 2025 Annual MD&A, audited consolidated financial statements, Annual Information Form and annual report on Form 40-F (filed with the
U.S. Securities and Exchange Commission) are available online at www.bmo.com/investorrelations and at www.sedarplus.ca. Printed copies of the
bank's complete 2025 audited consolidated financial statements are available free of charge upon request at 416-867-6785 or [email protected].
, /CNW/ - Bank of Montreal (TSX: BMO) (NYSE: BMO) today announced that its Board of Directors declared a quarterly dividend of $1.71 per share on paid-up common shares of Bank of Montreal for the third quarter of fiscal year 2026, a 4 cent, or 2 percent, increase from the prior quarter, up 5 percent from the prior year.
The Board of Directors also declared a dividend of:
$0.426 per share on paid-up Class B Preferred Shares Series 44. The dividend on the common shares is payable on August 26, 2026, to shareholders of record on July 30, 2026. The dividend on Class B Preferred Shares Series 44 is payable on August 25, 2026, to shareholders of record on July 30, 2026.
The above-mentioned dividends on the common and preferred shares are designated as "eligible" dividends for the purposes of the Income Tax Act (Canada) and any similar provincial and territorial legislation.
Common shareholders may elect to have their cash dividends reinvested in common shares of the Bank in accordance with the Bank's Shareholder Dividend Reinvestment and Share Purchase Plan (the "Plan"). Such additional common shares will be purchased on the open market without a discount until further notice.
For registered shareholders who wish to participate in the Plan, Enrolment Forms must be received by the Bank's transfer agent, Computershare Trust Company of Canada, by the close of business on August 3, 2026. Beneficial or non-registered holders must contact their financial institution or broker well in advance of the above date for instructions on how to participate.
More information about the Plan and how to enroll can be found at:
http://www.bmo.com/home/about/banking/investor-relations/shareholder-information/dividend-reinvestment-plan
BMO Financial Group (TSX:BMO), Bank of Nova Scotia (TSX:BNS) and National Bank of Canada (TSX:NA) all topped analyst expectations in their second-quarter results, with each bank raising its quarterly dividend.
BMO posted the most dramatic profit surge of the three, with net income climbing 34% year-over-year to $2.63 billion, or $3.53 per diluted share, for the quarter ended April 30.
On an adjusted basis, earnings reached $3.67 per diluted share, well ahead of the consensus estimate of $3.45.
Revenue rose to $9.57 billion from $8.68 billion a year earlier, while provisions for credit losses fell sharply to $739 million from $1.05 billion. The bank raised its quarterly dividend to $1.71 per share from $1.67.
Jefferies noted the beat was strong but flagged that much of the upside came from capital markets rather than domestic retail, which underperformed.
BMO also announced the sale of its Transportation and Vendor Finance businesses to Stonepeak, a move expected to trigger a $1.1 billion charge next quarter.
Scotiabank kicked off the reporting season with adjusted earnings of $2.02 per share, topping the consensus estimate of $1.93.
Provisions for credit losses came in at $1.22 billion, above the $1.11 billion estimate, though Jefferies said the result reflected continued efficiency gains and improving profitability across most operating segments.
The exception was Global Banking and Markets, which saw a modest sequential decline. Scotia's CET1 capital ratio held at 13.3%.
Jefferies raised its target price by $7 to $112, noting the bank is narrowing the gap to peers even as loan growth in its international segment remains negative.
National Bank rounded out the trio with adjusted earnings of $3.23 per share, beating the $3.14 estimate, on adjusted revenue of $3.918 billion against expectations of $3.81 billion.
Capital markets was a standout, with advisory fees up 35% sequentially.
National raised its quarterly dividend by 6.5% to $1.32 per share. Its CET1 ratio edged down 10 basis points to 13.5% following share repurchases.
Shares of Scotiabank rose 1.2% in Toronto trading, while BMO was flat and National Bank slipped 2.7%.
/CNW/ - CIBC (TSX: CM) (NYSE: CM) today announced senior leadership changes to its Group Executive Leadership Team. These changes will position the bank to
Royal Bank of Canada (TSX:RY), Toronto-Dominion Bank (TSX:TD) and Canadian Imperial Bank of Commerce (CIBC) (TSX:CM) all topped analyst profit estimates on Thursday, as strength in domestic banking and lower loan loss provisions helped the lenders navigate a challenging macroeconomic backdrop marked by US-Canada trade tensions.
The three banks largely benefited from strong growth at home and lower provisions for credit losses, or the money set aside to shield profits from souring loans.
Royal Bank posted adjusted earnings per share of C$3.90 for the quarter ended April 30, beating the C$3.79 estimate, as net income rose 25% year over year to C$5.5 billion.
Return on equity reached 17.2%, surpassing the bank's recently elevated 17% target.
Provisions for credit losses fell 36% year over year to C$912 million, accounting for much of the beat.
RBC raised its quarterly dividend 7% to C$1.76 per share and announced plans to repurchase up to 45 million common shares. Shares fell roughly 1%.
Toronto-Dominion reported adjusted EPS of C$2.38, ahead of the C$2.26 consensus, with record second-quarter earnings in Canadian Personal and Commercial Banking, Wealth Management, and Wholesale Banking. Canadian banking profit rose 15% year over year, while US retail adjusted net income grew 12% in US dollar terms. Provisions came in below expectations at C$1 billion.
TD raised its quarterly dividend 3.7% to C$1.12 per share. Shares slipped roughly 0.4%.
CIBC posted adjusted EPS of C$2.54, beating the C$2.42 estimate, lifted by capital markets strength. Revenue came in at C$8.01 billion against expectations of C$7.84 billion.
Alongside its results, the bank announced a deal to sell its 91.67% stake in CIBC Caribbean Bank Limited to The Bank of NT Butterfield & Son for approximately US$1.6 billion, comprising US$1 billion in cash and Butterfield shares currently valued at US$645 million. The stake represents an equity interest in Butterfield of approximately 22% at closing, with CIBC obtaining two seats on Butterfield's board. CIBC plans to invest a portion of the proceeds in US wealth manager &Partners. Shares dropped 4.8%.
All six of Canada's major banks surpassed profit estimates for the second quarter.
The International Atomic Energy Agency recently increased its projections for capacity of global nuclear power for a fifth straight year, and it now expects capacity to more than double by 2050. Still, nuclear energy is unfamiliar enough to many that it's easy for investors to be unaware of the intricacies of the nuclear fuel supply chain, including processes such as mining, enrichment, fabrication, reactor operation, waste disposal, and more.
With nuclear power in ever-increasing demand for data center applications and other uses, companies operating as pick-and-shovel plays within the nuclear supply chain could be positioned to benefit in a big way. Investors can therefore look beyond pure-play mining firms for an innovative approach to the nuclear energy space.
Get Centrus Energy alerts:
Major Provider of a Critical Enriched Product Sees Big Boost From DEA ContractCentrus Energy Corp. NYSE: LEU provides nuclear fuel enrichment services and is, in fact, the only American firm licensed to produce high-assay, low-enriched uranium (HALEU). This type of highly energy-dense uranium is vital for fueling many types of nuclear reactors—meaning that Centrus essentially has a monopoly on a critical corner of the market.
Centrus Energy Today
LEU
Centrus Energy
$146.66 -9.36 (-6.00%)
As of 06/10/2026 03:59 PM Eastern
This is a fair market value price provided by Massive. Learn more.
52-Week Range$144.65▼
$464.25P/E Ratio48.56
Price Target$268.18
This advantageous position has led to significant wins for Centrus in recent quarters. Late in 2025, for example, the company won a $900-million HALEU enrichment award from the Department of Energy. Structured as a procurement, the award will help Centrus to increase its HALEU production capacity. All of this has led to strong finances for Centrus. In 2025, revenue climbed to nearly $449 million, while backlog reached $3.8 billion, extending to 2040.
Although LEU shares have close to tripled in price in the last year, they are down fairly sharply this year, having fallen by about 10% year-to-date. Part of this has to do with a few precarious elements of its business, including its reliance on Russian supplies and its rapidly growing capital expenditures. Still, half of the analysts rating LEU view the stock as a Buy, and the consensus price target suggests nearly 25% in upside potential may be in store.
Low-Cost In-Situ Production Gives Uranium Energy Corp. a Margin EdgeWhen it comes to uranium mining firms, Uranium Energy Corp. NYSEAMERICAN: UEC stands out as a key—but often overlooked—domestic producer of yellowcake, the uranium concentrate that represents an intermediate step in uranium processing. In its latest quarter, Uranium Energy produced nearly 45,800 pounds of the substance.
Uranium Energy Today
UEC
Uranium Energy
$9.42 -1.23 (-11.55%)
As of 06/10/2026 04:10 PM Eastern
52-Week Range$5.90▼
$20.34Price Target$17.41
What makes Uranium Energy important for investors to know is that its in-situ recovery process keeps costs quite low—during the same period, the cash cost to the firm was only about $40 per pound of yellowcake. During the same period, it sold some 200,000 pounds of yellowcake for more than $100 per pound, leading to $20 million in revenue and about half that much in gross profit.
Uranium's low-cost production process has helped it to amass a solid cash foundation of more than $800 million as of the latest earnings report and has kept it debt-free in the process. With nearly 1.5 million pounds of yellowcake inventory on hand, the company is well-positioned to continue to provide these raw materials to nuclear energy firms across the production cycle for the foreseeable future. This may be why, despite also tripling in the last year, shares of UEC are projected to continue to rise by about 16%.
Rapid Medical Industry Growth Fuels BWX's ExpansionBWX Technologies Inc. NYSE: BWXT is a provider of nuclear components and services, with a particular focus on propulsion systems for naval nuclear reactors. The company thus has a niche focus on the defense industry, but also produces small modular reactors and components for non-defense uses as well, including for the medical industry.
BWX Technologies Today
BWXT
BWX Technologies
$183.47 -5.49 (-2.90%)
As of 06/10/2026 03:59 PM Eastern
This is a fair market value price provided by Massive. Learn more.
52-Week Range$128.96▼
$241.82Dividend Yield0.59%
P/E Ratio49.06
Price Target$228.00
BWX's multi-sector approach has paid off well—last quarter, the company closed 2025 with revenue up 18% YOY and earnings per share up 20%. Free cash flow and adjusted EBITDA also climbed thanks to strong commercial operations. In particular, the company's medical segment reached $100 million in annual revenue. This makes BWX an appealing nuclear energy play for investors keen to explore beyond the data center application.
Acquisitions and new facilities are helping BWX to expand its reach rapidly, and the company has been able to do so without jeopardizing its financial position. Indeed, it reduced interest costs and increased its liquidity to $1.7 billion by the end of 2025. On top of all this, BWX also offers investors a modest dividend bonus. Analysts are strongly bullish on BWXT, as more than two-thirds of those rating the stock have called it a Buy or equivalent.
Should You Invest $1,000 in Centrus Energy Right Now?Before you consider Centrus Energy, you'll want to hear this.
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Centrus Energy Corp. (LEU - Free Report) is expected to deliver a year-over-year decline in earnings on higher revenues when it reports results for the quarter ended March 2026. This widely-known consensus outlook gives a good sense of the company's earnings picture, but how the actual results compare to these estimates is a powerful factor that could impact its near-term stock price.
The stock might move higher if these key numbers top expectations in the upcoming earnings report, which is expected to be released on May 5. On the other hand, if they miss, the stock may move lower.
While the sustainability of the immediate price change and future earnings expectations will mostly depend on management's discussion of business conditions on the earnings call, it's worth handicapping the probability of a positive EPS surprise.
Zacks Consensus EstimateThis company is expected to post quarterly earnings of $0.41 per share in its upcoming report, which represents a year-over-year change of -55%.
Revenues are expected to be $74.05 million, up 1.3% from the year-ago quarter.
Estimate Revisions TrendThe consensus EPS estimate for the quarter has been revised 11.52% lower over the last 30 days to the current level. This is essentially a reflection of how the covering analysts have collectively reassessed their initial estimates over this period.
Investors should keep in mind that the direction of estimate revisions by each of the covering analysts may not always get reflected in the aggregate change.
Price, Consensus and EPS Surprise
Earnings WhisperEstimate revisions ahead of a company's earnings release offer clues to the business conditions for the period whose results are coming out. Our proprietary surprise prediction model -- the Zacks Earnings ESP (Expected Surprise Prediction) -- has this insight at its core.
The Zacks Earnings ESP compares the Most Accurate Estimate to the Zacks Consensus Estimate for the quarter; the Most Accurate Estimate is a more recent version of the Zacks Consensus EPS estimate. The idea here is that analysts revising their estimates right before an earnings release have the latest information, which could potentially be more accurate than what they and others contributing to the consensus had predicted earlier.
Thus, a positive or negative Earnings ESP reading theoretically indicates the likely deviation of the actual earnings from the consensus estimate. However, the model's predictive power is significant for positive ESP readings only.
A positive Earnings ESP is a strong predictor of an earnings beat, particularly when combined with a Zacks Rank #1 (Strong Buy), 2 (Buy) or 3 (Hold). Our research shows that stocks with this combination produce a positive surprise nearly 70% of the time, and a solid Zacks Rank actually increases the predictive power of Earnings ESP.
Please note that a negative Earnings ESP reading is not indicative of an earnings miss. Our research shows that it is difficult to predict an earnings beat with any degree of confidence for stocks with negative Earnings ESP readings and/or Zacks Rank of 4 (Sell) or 5 (Strong Sell).
How Have the Numbers Shaped Up for Centrus Energy?For Centrus Energy, the Most Accurate Estimate is lower than the Zacks Consensus Estimate, suggesting that analysts have recently become bearish on the company's earnings prospects. This has resulted in an Earnings ESP of -19.79%.
On the other hand, the stock currently carries a Zacks Rank of #5.
So, this combination makes it difficult to conclusively predict that Centrus Energy will beat the consensus EPS estimate.
Does Earnings Surprise History Hold Any Clue?While calculating estimates for a company's future earnings, analysts often consider to what extent it has been able to match past consensus estimates. So, it's worth taking a look at the surprise history for gauging its influence on the upcoming number.
For the last reported quarter, it was expected that Centrus Energy would post earnings of $1.42 per share when it actually produced earnings of $0.79, delivering a surprise of -44.37%.
Over the last four quarters, the company has beaten consensus EPS estimates two times.
Bottom LineAn earnings beat or miss may not be the sole basis for a stock moving higher or lower. Many stocks end up losing ground despite an earnings beat due to other factors that disappoint investors. Similarly, unforeseen catalysts help a number of stocks gain despite an earnings miss.
That said, betting on stocks that are expected to beat earnings expectations does increase the odds of success. This is why it's worth checking a company's Earnings ESP and Zacks Rank ahead of its quarterly release. Make sure to utilize our Earnings ESP Filter to uncover the best stocks to buy or sell before they've reported.
Centrus Energy doesn't appear a compelling earnings-beat candidate. However, investors should pay attention to other factors too for betting on this stock or staying away from it ahead of its earnings release.
An Industry Player's Expected ResultsAnother stock from the Zacks Mining - Non Ferrous industry, Southern Copper (SCCO - Free Report) , is soon expected to post earnings of $1.77 per share for the quarter ended March 2026. This estimate indicates a year-over-year change of +48.7%. Revenues for the quarter are expected to be $4.26 billion, up 36.3% from the year-ago quarter.
Over the last 30 days, the consensus EPS estimate for Southern Copper has been revised 3.2% up to the current level. Nevertheless, the company now has an Earnings ESP of 0.00%, reflecting an equal Most Accurate Estimate.
When combined with a Zacks Rank of #3 (Hold), this Earnings ESP makes it difficult to conclusively predict that Southern Copper will beat the consensus EPS estimate. The company beat consensus EPS estimates in each of the trailing four quarters.
Stay on top of upcoming earnings announcements with the Zacks Earnings Calendar.
Key Takeaways Centrus Energy is set to report Q1 2026 results May 5, with revenues seen up 1% but EPS down 55%.LEU may benefit from higher uranium prices and a delayed shipment, boosting Q1 margins and revenues.Higher costs, SG&A and interest expenses are expected to pressure profitability despite pricing gains. Centrus Energy (LEU - Free Report) is set to release its first-quarter 2026 results on May 5, after market close.
The Zacks Consensus Estimate for Centrus Energy’s first-quarter revenues is pegged at $74 million, suggesting a modest year-over-year growth of 1%. Over the past 60 days, the earnings estimate for first-quarter 2026 has moved down 24.1% to 41 cents per share. The figure reflects a 55% decline from the year-ago quarter’s earnings of 91 cents per share.
Image Source: Zacks Investment Research
Centrus Energy’s Earnings Surprise HistoryOver the trailing four quarters, Centrus Energy’s earnings beat the Zacks Consensus Estimate twice and missed the same in the remaining two quarters. LEU has an average trailing four-quarter earnings surprise of 266.12%. The trend is shown in the chart below.
Image Source: Zacks Investment Research
What the Zacks Model Unveils for LEUOur proven model does not conclusively predict an earnings beat for Centrus Energy this time around. The combination of a positive Earnings ESP and a Zacks Rank #1 (Strong Buy), 2 (Buy) or 3 (Hold) increases the odds of an earnings beat. But that is not the case here.
You can uncover the best stocks before they are reported with our Earnings ESP Filter.
Earnings ESP: The Earnings ESP for Centrus Energy is -21.41%.
Zacks Rank: LEU currently carries a Zacks Rank #5 (Strong Sell). You can see the complete list of today’s Zacks #1 Rank stocks here.
Factors Likely to Have Shaped Centrus Energy’s Q1 PerformanceCentrus Energy’s total revenues were down 3.6% to $146 million in the fourth quarter of 2025. The Low-Enriched Uranium segment’s revenues rose 2% year over year to $124.4 million. This was mainly led by separative work unit (SWU) revenues, which surged 128% year over year to $111.0 million, reflecting strong delivery timing. Uranium revenues collapsed 82% to $13.4 million due to a high base from a one-time sale in the prior year. The Technical Solutions segment’s revenues declined 27% to $21.8 million.
Centrus Energy reported fourth-quarter 2025 earnings per share of 79 cents, which marked a sharp 75% decline from $3.20 in the year-ago quarter.
A scheduled late-quarter shipment from Russia did not depart in time and was pushed into the first quarter of 2026. Management stated this shipment would have reduced average cost per SWU and supported higher gross margins and net income (or earnings) in the fourth quarter of 2025 if received as planned. This benefit is now expected to be reflected in the first quarter results, assuming the shipment was received as anticipated.
Overall, uranium prices averaged approximately $88.50 per pound in the first quarter of 2026, marking a 34% year-over-year increase. We expect Centrus Energy to have capitalized on this pricing environment by selling some uranium during the quarter, supporting revenues in the LEU segment.
For context, in the year-ago quarter, revenues for the Low-Enriched Uranium segment were reported at $51.3 million, which comprised revenues mainly from the sale of SWUs. The company had not made any uranium sales in that quarter. Revenues from the Technical Solutions segment were $21.8 million.
However, higher costs are expected to have weighed on profitability. Cost of sales is expected to have been higher for both the segments in the first quarter, due to higher volumes and an increase in costs incurred under the HALEU Operation Contract in the Technical Solutions segment. Also, increased selling, general and administrative expenses and interest expenses are likely to have dented earnings in the quarter.
LEU’s Price PerformanceCentrus Energy has skyrocketed 215.4% in a year compared with the industry’s 83% growth.
Image Source: Zacks Investment Research
How are Centrus Energy’s Peers Placed in Q1?Energy Fuels Inc. (UUUU - Free Report) is slated to announce first-quarter 2026 results on May 6. The Zacks Consensus Estimate for Energy Fuels’ earnings for the quarter has moved up from a loss of four cents to a loss of three cents over the past 60 days. It indicates an improvement from the loss of 13 cents reported in the first quarter of 2025. Energy Fuels has a negative average earnings surprise od 77.95% over the trailing four quarters. Energy Fuels currently carries a Zacks Rank #2 (Buy).
Cameco Corporation (CCJ - Free Report) is scheduled to report first-quarter 2026 results on May 5. The Zacks Consensus Estimate for Cameco’s first-quarter earnings per share is pegged at 29 cents. It indicates a 163% improvement from the prior-year quarter’s earnings. Over the past 60 days, the estimate has moved down 17.1%. Cameco has a negative average earnings surprise of 12.02% over the trailing four quarters. Cameco currently carries a Zacks Rank #3 (Hold).
A Stock to ConsiderHere is one Basic Materials stock, which according to our model, has the right combination of elements to post an earnings beat in its upcoming release.
CF Industries (CF - Free Report) , scheduled to release first-quarter 2026 earnings on May 6, currently has an Earnings ESP of +1.07% and a Zacks Rank of 1.
CF Industries’ earnings for the quarter are pegged at $2.35 per share, indicating year-over-year growth of 27%. The company has delivered a trailing four-quarter average earnings surprise of 13.15%.
Coeur Mining (CDE - Free Report) is expected to deliver a year-over-year increase in earnings on higher revenues when it reports results for the quarter ended March 2026. This widely-known consensus outlook gives a good sense of the company's earnings picture, but how the actual results compare to these estimates is a powerful factor that could impact its near-term stock price.
The stock might move higher if these key numbers top expectations in the upcoming earnings report, which is expected to be released on May 6. On the other hand, if they miss, the stock may move lower.
While management's discussion of business conditions on the earnings call will mostly determine the sustainability of the immediate price change and future earnings expectations, it's worth having a handicapping insight into the odds of a positive EPS surprise.
Zacks Consensus EstimateThis silver mining company is expected to post quarterly earnings of $0.44 per share in its upcoming report, which represents a year-over-year change of +300%.
Revenues are expected to be $794.1 million, up 120.6% from the year-ago quarter.
Estimate Revisions TrendThe consensus EPS estimate for the quarter has been revised 17.53% lower over the last 30 days to the current level. This is essentially a reflection of how the covering analysts have collectively reassessed their initial estimates over this period.
Investors should keep in mind that the direction of estimate revisions by each of the covering analysts may not always get reflected in the aggregate change.
Price, Consensus and EPS Surprise
Earnings WhisperEstimate revisions ahead of a company's earnings release offer clues to the business conditions for the period whose results are coming out. This insight is at the core of our proprietary surprise prediction model -- the Zacks Earnings ESP (Expected Surprise Prediction).
The Zacks Earnings ESP compares the Most Accurate Estimate to the Zacks Consensus Estimate for the quarter; the Most Accurate Estimate is a more recent version of the Zacks Consensus EPS estimate. The idea here is that analysts revising their estimates right before an earnings release have the latest information, which could potentially be more accurate than what they and others contributing to the consensus had predicted earlier.
Thus, a positive or negative Earnings ESP reading theoretically indicates the likely deviation of the actual earnings from the consensus estimate. However, the model's predictive power is significant for positive ESP readings only.
A positive Earnings ESP is a strong predictor of an earnings beat, particularly when combined with a Zacks Rank #1 (Strong Buy), 2 (Buy) or 3 (Hold). Our research shows that stocks with this combination produce a positive surprise nearly 70% of the time, and a solid Zacks Rank actually increases the predictive power of Earnings ESP.
Please note that a negative Earnings ESP reading is not indicative of an earnings miss. Our research shows that it is difficult to predict an earnings beat with any degree of confidence for stocks with negative Earnings ESP readings and/or Zacks Rank of 4 (Sell) or 5 (Strong Sell).
How Have the Numbers Shaped Up for Coeur Mining?For Coeur Mining, the Most Accurate Estimate is lower than the Zacks Consensus Estimate, suggesting that analysts have recently become bearish on the company's earnings prospects. This has resulted in an Earnings ESP of -14.12%.
On the other hand, the stock currently carries a Zacks Rank of #3.
So, this combination makes it difficult to conclusively predict that Coeur Mining will beat the consensus EPS estimate.
Does Earnings Surprise History Hold Any Clue?Analysts often consider to what extent a company has been able to match consensus estimates in the past while calculating their estimates for its future earnings. So, it's worth taking a look at the surprise history for gauging its influence on the upcoming number.
For the last reported quarter, it was expected that Coeur Mining would post earnings of $0.43 per share when it actually produced earnings of $0.35, delivering a surprise of -18.60%.
Over the last four quarters, the company has beaten consensus EPS estimates two times.
Bottom LineAn earnings beat or miss may not be the sole basis for a stock moving higher or lower. Many stocks end up losing ground despite an earnings beat due to other factors that disappoint investors. Similarly, unforeseen catalysts help a number of stocks gain despite an earnings miss.
That said, betting on stocks that are expected to beat earnings expectations does increase the odds of success. This is why it's worth checking a company's Earnings ESP and Zacks Rank ahead of its quarterly release. Make sure to utilize our Earnings ESP Filter to uncover the best stocks to buy or sell before they've reported.
Coeur Mining doesn't appear a compelling earnings-beat candidate. However, investors should pay attention to other factors too for betting on this stock or staying away from it ahead of its earnings release.
Expected Results of an Industry PlayerCentrus Energy Corp. (LEU - Free Report) , another stock in the Zacks Mining - Non Ferrous industry, is expected to report earnings per share of $0.41 for the quarter ended March 2026. This estimate points to a year-over-year change of -55%. Revenues for the quarter are expected to be $74.05 million, up 1.3% from the year-ago quarter.
The consensus EPS estimate for Centrus Energy has been revised 11.5% lower over the last 30 days to the current level. However, a lower Most Accurate Estimate has resulted in an Earnings ESP of -19.79%.
This Earnings ESP, combined with its Zacks Rank #3 (Hold), makes it difficult to conclusively predict that Centrus Energy will beat the consensus EPS estimate. Over the last four quarters, the company surpassed consensus EPS estimates two times.
Stay on top of upcoming earnings announcements with the Zacks Earnings Calendar.
Revenue of $76.7 million, compared to revenue of $73.1 million in Q1 2025 GAAP net income of $10.0 million compared to GAAP net income of $27.2 million in Q1 2025 Non-GAAP adjusted net income (1) of $23.5 million, compared to non-GAAP adjusted net income(1) of $28.6 million in Q1 2025 Launched multi-year investment in Oak Ridge, Tennessee, to expand and accelerate centrifuge manufacturing program Signed strategic collaboration with Fluor to oversee engineering, design, project management, supply chain activities, and procurement of key materials and services on plant expansion Partnered with Palantir to leverage its artificial intelligence platform; early work identified ~$300 million in potential costs savings and additional improvements expected to reduce manufacturing lead times and accelerate expansion's timetable Exploring joint-venture with Oklo focused on deconversion services for high-assay, low-enriched uranium (HALEU) Raising full year 2026 revenue guidance based on commercial progress , /PRNewswire/ -- Centrus Energy Corp. (NYSE: LEU) ("Centrus" or the "Company") today reported first quarter 2026 results. The Company reported net income of $10.0 million for the three months ended March 31, 2026, which is $0.51 (basic) and $0.45 (diluted) per common share. This translates to adjusted net income(1) of $23.5 million for the three months ended March 31, 2026, which is adjusted EPS(1) of $1.19 (basic) and $1.05 (diluted) per common share.
"The first quarter was marked by numerous wins and great operational progress as we accelerated our drive to restore America's ability to enrich uranium at scale, including securing historic federal funding and launching a major expansion of our centrifuge manufacturing plant," said Centrus President and CEO Amir Vexler.
"We have now switched to full execution mode to accelerate our build-out while building a best-in-class partnership network, including Palantir, Fluor, and Geiger Brothers, as part of our day-one focus to reduce costs and bring in lead times. We've already identified approximately $300 million in cost reductions as well as opportunities to both reduce manufacturing lead times and accelerate our timetable. Going forward we will continue to unleash our network's full capabilities, including Palantir's leading artificial intelligence platform, to unlock more efficiency gains.
"Our expansion is well timed. Global conflicts and rising tensions continue to highlight the need to diversify away from fossil fuels towards domestic power sources to drive future sustainable economic growth."
(1)A reconciliation of non-GAAP results are detailed in the Financial Results section. Additional information can be found in the materials on the Centrus investor relations website at https://investors.centrusenergy.com.
Financial Results
Centrus generated total revenue of $76.7 million and $73.1 million for the three months ended March 31, 2026 and 2025, respectively, an increase of $3.6 million (or 5%).
Revenue from the LEU segment was $44.6 million and $51.3 million for the three months ended March 31, 2026 and 2025, respectively, a decrease of $6.7 million (or 13%). Separative work units (SWU) revenue decreased by $9.7 million as a result of a 47% decrease in the volume of SWU sold, partially offset by a 52% increase in the average price of SWU sold. The Company had uranium revenue of $3.0 million for the three months ended March 31, 2026.
Revenue from the Technical Solutions segment was $32.1 million and $21.8 million for the three months ended March 31, 2026 and 2025, respectively, an increase of $10.3 million (or 47%). The increase in revenue was primarily attributable to a $9.8 million increase in revenue generated by the HALEU production contract with the Department of Energy ("DOE") signed in 2022 ("HALEU Operation Contract"), while the remaining change was generally related to other contracts. Revenue from the HALEU Operation Contract is recorded on a cost-plus-incentive-fee basis and includes a target fee for Phases 2 and 3 of the contract.
Cost of sales for the LEU segment was $16.7 million and $20.1 million for the three months ended March 31, 2026 and 2025, respectively, a decrease of $3.4 million (or 17%). SWU costs decreased as a result of a 47% decrease in the volume of SWU sold, partially offset by a 45% increase in the average unit cost of SWU sold. Uranium costs increased primarily as a result of an increase in the volume of uranium sold.
Cost of sales for the Technical Solutions segment was $28.5 million and $20.1 million for the three months ended March 31, 2026 and 2025, respectively, an increase of $8.4 million (or 42%). The increase was primarily attributable to an $8.2 million increase in costs incurred under the HALEU Operation Contract, while the remaining change was generally attributable to other contracts.
The Company recognized gross profit of $31.5 million and a gross profit of $32.9 million for the three months ended March 31, 2026 and 2025, respectively, a decrease of $1.4 million (or 4%).
Gross profit for the LEU segment was $27.9 million and $31.2 million for the three months ended March 31, 2026 and 2025, respectively, a decrease of $3.3 million (or 11%). LEU customers generally have multi-year contracts that carry annual purchase commitments, not quarterly commitments. The gross profit in our LEU business varies based upon the timing of those contracts. The pricing applied to deliveries varies depending upon the market conditions at the time the contract was signed. The increase for the three months ended March 31, 2026 was primarily due to the composition of contracts in the current quarter, compared to the prior quarter.
Gross profit for the Technical Solutions segment was $3.6 million and $1.7 million for the three months ended March 31, 2026 and 2025, respectively, an increase of $1.9 million (or 112%). Because of the delay in completing Phase 2 of the HALEU Operation Contract, DOE extended the Phase 2 period of performance through October 31, 2025. Costs incurred subsequent to November 2024 have not yet been subject to a fee as this portion of Phase 2 remains undefinitized and is subject to negotiation.
Net income was $10.0 million and $27.2 million for the three months ended March 31, 2026 and 2025, respectively, a decrease of $17.2 million (or 63%). The decrease was primarily attributable to an increase in advanced technology costs of $15.9 million and a decrease in extinguishment of long-term debt of $11.8 million. This decrease was partially offset by an increase of $9.7 million in investment income and a decrease of $5.5 million in income tax expense.
Backlog
The Company's backlog across both segments is $3.9 billion as of March 31, 2026 and extends to 2040. Our LEU segment backlog as of March 31, 2026 is approximately $3.1 billion. The LEU backlog is the estimated aggregate dollar amount of revenue for future SWU and uranium deliveries primarily under medium and long-term contracts with fixed commitments and approximately $2.4 billion in contingent LEU sales commitments, all of which are under definitive agreements, in support of potential construction of LEU production capacity at the Piketon, Ohio facility. The contingent LEU sales commitments also depend on our ability to secure substantial public and private investment. Our Technical Solutions segment backlog is approximately $0.8 billion as of March 31, 2026, and includes both funded amounts (services for which funding has been both authorized and appropriated by the customer), unfunded amounts (services for which funding has not been appropriated), and unexercised options.
2026 Outlook
The Company is updating some of its financial and operational guidance for the full-year 2026 based on information available to the Company at the time of this release.
Financial 2026 Outlook
For the full year 2026, on a consolidated basis, Centrus expects:
Upward revised total revenue to be in the range of $450 million to $500 million from $425 million to $475 million Total capital deployment to be in the range of $350 million to $500 million, driven by increased investment in the Company's industrial build out related to its centrifuge manufacturing Operational 2026 Outlook
For the full year 2026, on a consolidated basis, Centrus expects to:
Finalize contracts with all partners identified as critical to its industrial build out At least 100 net new employee hires for Oak Ridge, Tennessee, facility At least 100 net new employee hires for Piketon, Ohio, facility up from 50 net new employee hires Release of a Certified for Construction package The Company's 2026 guidance is subject to a number of assumptions and uncertainties that could affect results either positively or negatively. Variations from these expectations could cause differences between this guidance and the ultimate results. This includes the assumption of no significant change in restrictions in our ability to receive and sell Russian LEU or other uranium products, no significant economic disruptions or downturns, the successful implementation of our planned expansion projects, including the finalization and funding of the DOE $900 million task order, and that current business operations will continue on an ongoing basis.
About Centrus Energy Corp.
Centrus Energy is a trusted American supplier of nuclear fuel and services for the nuclear power industry, helping meet the growing need for clean, affordable, carbon-free energy. Since 1998, the Company has provided its utility customers with more than 1,850 reactor years of fuel, which is equivalent to more than 7 billion tons of coal.
With world-class technical and engineering capabilities, Centrus is pioneering production of High-Assay, Low-Enriched Uranium and is leading the effort to restore America's uranium enrichment capabilities at scale so that we can meet our clean energy, energy security, and national security needs. Find out more at www.centrusenergy.com or follow us on LinkedIn and X.
Forward-Looking Statements:
This news release contains "forward-looking statements" within the meaning of Section 21E of the Securities Exchange Act of 1934, as amended, and the Private Securities Litigation Reform Act of 1995. In this context, forward-looking statements mean statements related to future events, which may impact our expected future business and financial performance, and often contain words such as "expects", "anticipates", "intends", "plans", "believes", "will", "should", "could", "would" or "may" and other words of similar meaning. These forward-looking statements are based on information available to us as of the date of this news release and represent management's current views and assumptions with respect to future events and operational, economic and financial performance. Forward-looking statements are not guarantees of future performance, events or results and involve known and unknown risks, uncertainties and other factors, which may be beyond our control, and which may be exacerbated by any worsening of the global business and economic environment, including but not limited to, risks and uncertainties related to the following:
the war in Ukraine and other geopolitical conflicts, including the resulting bans, laws, tariffs, sanctions or other government measures, and actions by third parties, including contractual counterparties, as a result of such conflicts that could directly or indirectly impact our ability to obtain, deliver, transport, sell or collect payment for, LEU or the SWU and natural uranium hexafluoride components of LEU; our reliance on third party suppliers to provide essential products and services to us; restrictions on imports and exports, including those imposed under the RSA, and related international trade legislation; our lease to our facility in Piketon, Ohio and our government contracts, including related to government shutdowns, changes to the U.S. government's appropriated funding levels for HALEU and the government's inability to satisfy its obligations; our receipt of additional task orders under the HALEU Production Contract, LEU Production Contract and HALEU Deconversion Contract and, if awarded, the nature, timing and amount thereof; our ability to obtain new contracts or funding to be able to continue operations; whether or when government demand for HALEU or LEU for government or commercial uses will materialize and at what level; the impact and potential extended duration of a supply/demand imbalance in the market for LEU; significant competition from major LEU producers, including foreign competitors, who may be less cost sensitive than we are; limitations on our ability to compete in foreign markets; pricing trends and demand in the uranium and enrichment markets, especially in light of the potential of limited supply and our dependence on others for deliveries of LEU; our ability to successfully implement our planned expansion projects in Piketon, Ohio and Oak Ridge, Tennessee; our ability to successfully integrate artificial intelligence technologies into our operations; natural and other disasters; pandemics and other health crises; the fact that our revenue is largely dependent on our largest customers and our sales backlog; our long-term liabilities, including our postretirement health and life benefit obligations, our 0% Convertible Notes and our 2.25% Convertible Notes; failures or security, including cybersecurity, breaches of our information technology systems; and the impact of, or changes to, government regulation and policies or interpretation of laws or regulations, including by the U.S. Securities and Exchange Commission, the DOE, the U.S. Department of Commerce, and the U.S. Nuclear Regulatory Commission. Readers are cautioned not to place undue reliance on these forward-looking statements, which apply only as of the date of this news release. These factors may not constitute all factors that could cause actual results to differ from those discussed in any forward-looking statement. Accordingly, forward-looking statements should not be relied upon as a predictor of actual results. Readers are urged to carefully review and consider the various disclosures made in this news release and in our filings with the SEC, including our Annual Report on Form 10-K for the year ended December 31, 2025, under Part II, Item 1A - "Risk Factors" in our Quarterly report on Form 10-Q for the quarter ended March 31, 2026, and our filings with the SEC that attempt to advise interested parties of the risks and factors that may affect our business. We do not undertake to update our forward-looking statements to reflect events or circumstances that may arise after the date of this news release, except as required by law.
Contacts:
Investors: Neal Nagarajan at [email protected]
Media: Dan Leistikow at [email protected]
CENTRUS ENERGY CORP.
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS AND COMPREHENSIVE INCOME
(Unaudited; in millions, except share and per share data)
Three Months Ended
March 31,
2026
2025
Revenue:
Separative work units
$ 41.6
$ 51.3
Uranium
3.0
—
Technical solutions
32.1
21.8
Total revenue
76.7
73.1
Cost of Sales:
Separative work units and uranium
16.7
20.1
Technical solutions
28.5
20.1
Total cost of sales
45.2
40.2
Gross profit
31.5
32.9
Advanced technology costs
18.9
3.0
Selling, general and administrative
10.0
8.3
Amortization of intangible assets
1.8
1.1
Operating income
0.8
20.5
Nonoperating components of net periodic benefit loss
1.0
0.9
Interest expense
4.0
3.4
Investment income
(17.0)
(7.3)
Extinguishment of long-term debt
—
(11.8)
Other expense, net
0.3
0.1
Income before income taxes
12.5
35.2
Income tax expense
2.5
8.0
Net income and comprehensive income
$ 10.0
$ 27.2
Net income per share:
Basic
$ 0.51
$ 1.60
Diluted
$ 0.45
$ 1.60
Average number of common shares outstanding (in thousands):
Basic
19,773
16,982
Diluted
22,446
17,048
CENTRUS ENERGY CORP.
NON-GAAP ADJUSTED OPERATING INCOME, ADJUSTED NET INCOME AND
ADJUSTED NET INCOME PER SHARE RECONCILIATION TABLE
The Company measures Operating Income, Net Income and Net Income per Share both on a GAAP basis and on an adjusted basis ("Adjusted Operating Income", "Adjusted Net Income" and "Adjusted Net Income per Share") to exclude short-term, non-capitalizable costs related to the expansion of our operations in Piketon, Ohio and Oak Ridge, Tennessee to scale up uranium enrichment operations ("Growth Costs") and stock-based compensation. Growth Costs relate to the initial phase of our expansion projects (e.g. manufacturing readiness and the training and onboarding of new employees) and are included as Advanced Technology Costs on the Condensed Consolidated Statements of Operations and Comprehensive Income. The Company expects to stop expensing Growth Costs as costs related to our expansion projects become capitalizable. We incur expense related to stock-based compensation which are included as Selling, General and Administrative expense on the Condensed Consolidated Statements of Operations and Comprehensive Income.
We believe Adjusted Operating Income, Adjusted Net Income and Adjusted Net Income per Share, which are non-GAAP financial measures, provide investors with additional understanding of the Company's overall financial performance as well as its strategic financial planning analysis and period-to-period comparability. These metrics are useful to investors because they reflect how management evaluates the Company's ongoing operating performance from period-to-period after removing certain transactions and activities that affect comparability of the metrics and are not reflective of the Company's core operations.
Our calculation of Adjusted Operating Income, Adjusted Net Income, and Adjusted Net Income per Share may not be comparable to similarly named measures reported by other companies.
Three Months Ended March 31, 2026
Three Months Ended March 31, 2025
GAAP
Growth
Costs
Stock-
Based
Compen
sation
Adjusted
(Non-
GAAP)
GAAP
Growth
Costs
Stock-
Based
Compen
sation
Adjusted
(Non-
GAAP)
Gross profit
31.5
—
—
31.5
32.9
—
—
32.9
Advanced technology costs
18.9
(17.0)
—
1.9
3.0
(1.3)
—
1.7
Selling, general and administrative
10.0
—
(0.4)
9.6
8.3
—
(0.5)
7.8
Amortization of intangible assets
1.8
—
—
1.8
1.1
—
—
1.1
Operating income
0.8
17.0
0.4
18.2
20.5
1.3
0.5
22.3
Nonoperating components of net
periodic benefit loss
1.0
—
—
1.0
0.9
—
—
0.9
Interest expense
4.0
—
—
4.0
3.4
—
—
3.4
Investment income
(17.0)
—
—
(17.0)
(7.3)
—
—
(7.3)
Extinguishment of long-term
debt
—
—
—
—
(11.8)
—
—
(11.8)
Other expense, net
0.3
—
—
0.3
0.1
—
—
0.1
Income before income taxes
12.5
17.0
0.4
29.9
35.2
1.3
0.5
37.0
Income tax expense
2.5
3.8
0.1
6.4
8.0
0.3
0.1
8.4
Net income and comprehensive
income
$ 10.0
$ 13.2
$ 0.3
$ 23.5
$ 27.2
$ 1.0
$ 0.4
$ 28.6
Net income per share:
Basic
$ 0.51
$ 0.67
$ 0.01
$ 1.19
$ 1.60
$ 0.06
$ 0.02
$ 1.68
Diluted
$ 0.45
$ 0.59
$ 0.01
$ 1.05
$ 1.60
$ 0.06
$ 0.02
$ 1.68
Average number of common
shares outstanding (in
thousands):
Basic
19,773
—
—
19,773
16,982
—
—
16,982
Diluted
22,446
—
—
22,446
17,048
—
—
17,048
CENTRUS ENERGY CORP.
CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS
(Unaudited; in millions)
Three Months Ended March 31,
2026
2025
OPERATING
Net income
$ 10.0
$ 27.2
Adjustments to reconcile net income to cash used in operating activities:
Depreciation and amortization
2.2
1.5
Deferred tax assets
2.5
7.5
Equity-related compensation
0.4
0.5
Revaluation of inventory borrowings
(0.6)
2.1
Gain on extinguishment of 8.25% Notes
—
(11.8)
Amortization of debt issuance costs and discount
1.3
—
Other reconciling adjustments, net
0.3
0.6
Changes in operating assets and liabilities:
Accounts receivable
(11.1)
41.3
Inventories
(48.8)
(268.1)
Inventories owed to customers and suppliers
(21.9)
187.7
Other current assets
(0.6)
0.8
Accounts payable and other liabilities
0.4
(6.2)
Payables under inventory purchase agreements
47.2
55.6
Deferred revenue and advances from customers, net of deferred costs
(14.4)
0.1
Pension and postretirement benefit liabilities
(2.0)
(2.2)
Other changes, net
—
(0.1)
Cash (used in) provided by operating activities
(35.1)
36.5
INVESTING
Capital expenditures
(23.2)
(2.1)
Cash used in investing activities
(23.2)
(2.1)
FINANCING
Proceeds from the issuance of common stock, net
—
25.2
Common stock withheld for tax obligations under stock-based compensation plan
(0.3)
—
Payment of interest classified as debt
—
(3.5)
Payment of principal to redeem 8.25% Notes
—
(74.3)
Cash used in financing activities
(0.3)
(52.6)
Effect of exchange rate changes on cash, cash equivalents and restricted cash
(0.3)
(0.1)
Decrease in cash, cash equivalents and restricted cash
(58.9)
(18.3)
Cash, cash equivalents and restricted cash, beginning of period
1,960.1
704.0
Cash, cash equivalents and restricted cash, end of period
$ 1,901.2
$ 685.7
Three Months Ended March 31,
2026
2025
Supplemental cash flow disclosures:
Cash paid for interest
—
$ —
Cash paid for income taxes
Federal
—
$ —
State
—
$ —
Foreign
—
$ —
Non-cash activities:
Property, plant and equipment included in accounts payable and accrued liabilities
$ 9.2
$ 0.2
Common stock withheld for tax obligations under stock-based compensation plan
$ —
$ 0.3
CENTRUS ENERGY CORP.
CONDENSED CONSOLIDATED BALANCE SHEETS
(Unaudited; in millions, except share and per share data)
March 31,
2026
December 31,
2025
ASSETS
Current assets:
Cash and cash equivalents
$ 1,868.2
$ 1,957.2
Accounts receivable
41.8
30.7
Inventories
336.0
322.9
Deferred costs associated with deferred revenue
37.0
40.9
Other current assets
12.4
11.9
Total current assets
2,295.4
2,363.6
Property, plant and equipment, net of accumulated depreciation of $7.1 million and
$6.7 million as of March 31, 2026 and December 31, 2025, respectively
59.5
29.5
Deposits for financial assurance
32.8
2.7
Intangible assets, net
19.4
21.2
Deferred tax assets
19.5
21.9
Other long-term assets
6.6
7.0
Total assets
$ 2,433.2
$ 2,445.9
LIABILITIES AND STOCKHOLDERS' EQUITY
Current liabilities:
Accounts payable and accrued liabilities
$ 49.5
$ 41.6
Payables under inventory purchase agreements
65.7
18.5
Inventories owed to customers and suppliers
170.8
192.7
Deferred revenue and advances from customers
112.8
131.1
Short-term inventory loans
2.5
38.9
Current debt
—
—
Total current liabilities
401.3
422.8
Long-term debt
1,176.1
1,174.8
Postretirement health and life benefit obligations
70.4
72.2
Pension benefit liabilities
2.9
3.0
Advances from customers
—
—
Long-term inventory loans
—
—
Other long-term liabilities
7.3
8.0
Total liabilities
1,658.0
1,680.8
Stockholders' equity:
Preferred stock, par value $1.00 per share, 20,000,000 shares authorized
Series A Participating Cumulative Preferred Stock, none issued
—
—
Series B Senior Preferred Stock, none issued
—
—
Class A Common Stock, par value $0.10 per share, 70,000,000 shares authorized,
18,952,387 and 18,945,365 shares issued and outstanding as of March 31, 2026
and December 31, 2025, respectively
1.9
1.9
Class B Common Stock, par value $0.10 per share, 30,000,000 shares authorized,
719,200 shares issued and outstanding as of March 31, 2026 and December 31,
2025
Centrus Energy Corp. (LEU - Free Report) came out with quarterly earnings of $1.05 per share, beating the Zacks Consensus Estimate of $0.33 per share. This compares to earnings of $0.91 per share a year ago. These figures are adjusted for non-recurring items.
This quarterly report represents an earnings surprise of +216.84%. A quarter ago, it was expected that this company would post earnings of $1.42 per share when it actually produced earnings of $0.79, delivering a surprise of -44.37%.
Over the last four quarters, the company has surpassed consensus EPS estimates two times.
Centrus Energy, which belongs to the Zacks Mining - Non Ferrous industry, posted revenues of $76.7 million for the quarter ended March 2026, surpassing the Zacks Consensus Estimate by 0.74%. This compares to year-ago revenues of $73.1 million. The company has topped consensus revenue estimates three times over the last four quarters.
The sustainability of the stock's immediate price movement based on the recently-released numbers and future earnings expectations will mostly depend on management's commentary on the earnings call.
Centrus Energy shares have lost about 14.8% since the beginning of the year versus the S&P 500's gain of 5.2%.
What's Next for Centrus Energy?While Centrus Energy has underperformed the market so far this year, the question that comes to investors' minds is: what's next for the stock?
There are no easy answers to this key question, but one reliable measure that can help investors address this is the company's earnings outlook. Not only does this include current consensus earnings expectations for the coming quarter(s), but also how these expectations have changed lately.
Empirical research shows a strong correlation between near-term stock movements and trends in earnings estimate revisions. Investors can track such revisions by themselves or rely on a tried-and-tested rating tool like the Zacks Rank, which has an impressive track record of harnessing the power of earnings estimate revisions.
Ahead of this earnings release, the estimate revisions trend for Centrus Energy was mixed. While the magnitude and direction of estimate revisions could change following the company's just-released earnings report, the current status translates into a Zacks Rank #3 (Hold) for the stock. So, the shares are expected to perform in line with the market in the near future. You can see the complete list of today's Zacks #1 Rank (Strong Buy) stocks here.
It will be interesting to see how estimates for the coming quarters and the current fiscal year change in the days ahead. The current consensus EPS estimate is $0.94 on $146.7 million in revenues for the coming quarter and $2.66 on $466.16 million in revenues for the current fiscal year.
Investors should be mindful of the fact that the outlook for the industry can have a material impact on the performance of the stock as well. In terms of the Zacks Industry Rank, Mining - Non Ferrous is currently in the top 38% of the 250 plus Zacks industries. Our research shows that the top 50% of the Zacks-ranked industries outperform the bottom 50% by a factor of more than 2 to 1.
Lundin Mining (LUNMF - Free Report) , another stock in the same industry, has yet to report results for the quarter ended March 2026. The results are expected to be released on May 6.
This base metals mining company is expected to post quarterly earnings of $0.29 per share in its upcoming report, which represents a year-over-year change of +163.6%. The consensus EPS estimate for the quarter has been revised 3.5% higher over the last 30 days to the current level.
Lundin Mining's revenues are expected to be $1.12 billion, up 16% from the year-ago quarter.