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2026-06-12 11:47 1mo ago
2026-06-02 07:45 1mo ago
Even After the Monster Rally, These 5 Safe High-Yielding Energy Stocks Are Still Strong Buys
BEP Brookfield Renewable Partners
FMP Stock News
Original source text
This post may contain links from our sponsors and affiliates, and Flywheel Publishing may receive compensation for actions taken through them.

Many on Wall Street argue that oil prices could remain elevated regardless of how the Iran conflict resolves, for several structural reasons. Global spare capacity is largely concentrated in a handful of OPEC+ nations. It has grown increasingly thin, meaning any disruption to supply chains, shipping lanes, or refining infrastructure takes longer to be absorbed and worked through the system. The Strait of Hormuz remains a critical path for roughly 20% of the global oil trade, and even a ceasefire or de-escalation wouldn’t instantly restore insurer confidence or normalize tanker routing, keeping freight and risk premiums largely baked into prices.

Years of underinvestment in upstream exploration and production mean the supply side can’t respond quickly to demand signals the way it once could. Add to that a weaker dollar environment, persistent demand from emerging markets, particularly India and China, and OPEC+’s demonstrated willingness to defend price floors through coordinated cuts, and the conditions for structurally higher oil exist well beyond the current hostilities in the Middle East. The bottom line for investors is that if they are underweight or don’t own any energy names, now’s the time to consider adding some to a portfolio. But after a massive rally that started when the conflict with Iran began in late February, it makes sense to look at the safest energy companies now.

We decided to screen our 24/7 Wall St. energy stock database, looking for companies that still deliver large and dependable dividends while remaining good investments on a valuation basis. While we remain positive on the mega-cap integrated giants, they have had spectacular runs and would be much better purchases after a solid price pullback.

Five companies that pay significant dividends and offer shareholders some of the best valuations currently are at the top of our strong buy list for investors. All still offer reasonable entry points, with outstanding upside potential to the posted Wall Street target prices. All five are also rated Buy at the top Wall Street firms we cover at 24/7 Wall St.

Why do we cover the safest high-yielding energy dividend stocks? Since 1926, dividends have accounted for approximately 32% of the S&P 500’s total return, while capital appreciation has accounted for 68%. Therefore, sustainable dividend income and the potential for capital appreciation are essential to total return expectations. A study by Hartford Funds, in collaboration with Ned Davis Research, found that dividend stocks delivered an annualized return of 9.18% over the past 50 years (1973 to 2023). Over the same timeline, this was more than double the annualized return for non-payers (3.95%).

Brookfield Renewable Partners This off-the-radar utility stock is an ideal choice now for growth and income investors, as well as those concerned with environmental issues. Brookfield Renewable Partners (NYSE: BEP | BEP Price Prediction) operates publicly traded platforms for renewable power and decarbonization solutions. Investors are paid a rich 4.41% dividend. Earnings rose 15% in Q1 2026 and 12% over the trailing twelve months. The company expects double-digit earnings growth to continue for at least the next five years. Since going public in 2011, it has raised its dividend by at least 5% every year and targets dividend growth of 5% to 9% going forward.

The company’s renewable power portfolio includes:

Hydroelectric Wind Utility-scale solar Distributed generation Storage facilities located across North America, South America, Europe, and the Asia-Pacific region Its operations are divided into six segments:

Hydroelectric, which is further categorized by geography (North America, Colombia, and Brazil) Wind Utility-scale solar Distributed energy and storage, including distributed generation Pumped storage Battery energy storage systems; sustainable solutions, encompassing agricultural renewable natural gas, carbon capture and storage, recycling, cogeneration, biomass, nuclear services, electrofuels, and power transformation Corporate The company’s total power portfolio comprises approximately 46,200 megawatts of installed capacity and a development pipeline of approximately 200,000 megawatts.

TD Securities has a Buy rating with a $39 target price.

Clearwater Energy This is another off-the-radar company that is safe and still bargain-priced, with a strong 4.42% dividend. Clearwater Energy (NYSE: CWEN) is a renewable energy company that invests in energy infrastructure, focuses on clean energy, and owns modern, sustainable, and long-term-contracted assets across North America. It is one of the largest renewable energy companies in the U.S., with a portfolio of wind, solar, and energy storage facilities across 27 states totaling approximately 12.7 gigawatts of gross capacity. Both share classes have risen more than 20% over the past 12 months. The data center boom has been a significant growth driver.

Clearwater Energy’s operating facilities include:

Carlsbad El Segundo GenConn Devon GenConn Middletown Marsh Landing Walnut Creek The company’s utility-scale solar projects include:

Agua Caliente Alpine Avenal Avra Valley Blythe Borrego Buckthorn Solar CVSR Daggett 2 Daggett 3 Desert Sunlight 250 Kansas South The company’s wind projects include Black Rock, Buffalo Bear, Cedro Hill, Crofton Bluffs, and Cedar Creek.

UBS has a Buy rating with a $45 target price.

Enbridge Enbridge owns and operates pipelines throughout Canada and the United States. This is an off-the-radar idea based in Canada, poised to break out to new highs soon, and pays a rich 6.94% dividend. Enbridge (NYSE: ENB) operates as an energy infrastructure company. Enbridge announced its 31st consecutive annual dividend increase in 2026, lifting the payout by another 3%, and has paid dividends for over 70 years. With roughly 98% of its annual earnings backed by long-term, fixed-rate contracts and regulated rate structures, the company stands out as one of the most defensive and reliable plays in the energy infrastructure sector.

The company operates through five segments:

Liquids Pipelines Gas Transmission and Midstream Gas Distribution and Storage Renewable Power Generation Energy Services The Liquids Pipelines segment operates pipelines and related terminals in Canada and the United States to transport various grades of crude oil and other liquid hydrocarbons.

The Gas Transmission and Midstream segment invests in natural gas pipelines and gathering and processing facilities in Canada and the United States. The Gas Distribution and Storage segment is involved in natural gas utility operations, serving residential, commercial, and industrial customers in Ontario, as well as in natural gas distribution and energy transportation activities in Quebec.

The Renewable Power Generation segment operates power-generating assets, including wind, solar, geothermal, and waste heat recovery facilities, as well as transmission assets, in North America and Europe. The Energy Services segment provides energy marketing services to refiners, producers, and other customers, as well as physical commodity marketing and logistical services in Canada and the United States.

Royal Bank of Canada has an Outperform rating and a $79 target price.

Energy Transfer Energy Transfer (NYSE: ET) is one of North America’s largest and most diversified midstream energy companies. This top master limited partnership is a safe option for investors seeking energy exposure and income, as the company pays a 6.67% distribution yield. It owns and operates one of the largest and most diversified portfolios of energy assets in the United States, with a strategic footprint across all major domestic production basins. As a midstream MLP, its revenue is largely fee-based and less sensitive to commodity price swings.

The company is a publicly traded limited partnership with core operations that include:

Complementary natural gas midstream, intrastate, and interstate transportation and storage assets Crude oil, natural gas liquids (NGL), and refined product transportation and terminalling assets NGL fractionation Various acquisition and marketing assets Following the acquisition of Enable Partners in December 2021, Energy Transfer owns and operates over 114,000 miles of pipelines and related assets in 41 states, spanning all major U.S. producing regions and markets. This solidifies its leadership position in the midstream sector.

Through its ownership of Energy Transfer Operating, formerly known as Energy Transfer Partners, the company also owns Lake Charles LNG; the general partner interests, the incentive distribution rights, and 28.5 million standard units of Sunoco (NYSE: SUN); and the public partner interests and 39.7 million standard units of USA Compression Partners (NYSE: USAC).

Stifel has a Buy rating on the shares, with a $25 target price.

Enterprise Products Partners This top midstream giant is an American midstream natural gas and crude oil pipeline company headquartered in Houston, Texas. Enterprise Products Partners (NYSE: EPD) is one of the most extensive publicly traded energy partnerships, and it pays a very reliable 5.84% dividend. The company’s debt-to-EBITDA ratio ranges from 3.1x to 3.4x, which is moderate for a midstream energy company, and its interest coverage ratio is 5x.

Enterprise Products Partners generates strong free cash flow, with an operating cash flow of approximately $8.8 billion, resulting in approximately $4.2 billion in free cash flow annually after deducting capital expenditures. Another significant benefit for shareholders is that most of the corporate debt is fixed-rate, thereby limiting the risk of rising interest rates.

It provides various midstream energy services, including:

Gathering Processing Transporting and storing natural gas, natural gas liquids (NGL), and fractionation Import and export terminalling Offshore production platform services The company has four reportable business segments:

Natural Gas Pipelines and Services NGL Pipelines and Services Petrochemical Services Crude Oil Pipelines and Services One reason many analysts like the stock might be its distribution coverage ratio. The company’s coverage ratio is well above 1x, making it relatively less risky among the MLPs.

Citigroup has a Buy rating with a $45 price objective.
2026-06-12 11:47 1mo ago
2026-06-02 09:00 1mo ago
3 High-Yield Dividend Stocks I Can't Wait to Buy in June to Boost My Passive Income
BEP Brookfield Renewable Partners
FMP Stock News
Original source text
My long-term financial goal is to generate enough passive income to cover my basic living expenses. Reaching that level of financial freedom would relieve some pressure and give me more flexibility.

A core aspect of my strategy is investing in high-yielding dividend stocks. I focus on companies that pay well-supported dividends that should grow in the future. Three of my favorites are Brookfield Infrastructure (BIPC 2.06%)(BIP 1.59%), Brookfield Renewable (BEPC +0.51%)(BEP +0.31%), and W.P. Carey (WPC 0.34%). Here's why I can't wait to buy more of each one this June.

Image source: Getty Images.

Megatrend-driven dividend growth Brookfield Infrastructure operates a globally diversified portfolio of crucial economic infrastructure across the utility, midstream, transport, and data sectors. The company's assets include pipelines, electricity transmission lines, toll roads, telecom towers, and data centers. These assets generate very stable, steadily rising cash flows, supported by long-term contracts and government-regulated rate structures with built-in inflation escalators (85% of its funds from operations, or FFO, in 2026).

The company aims to pay out between 60% and 70% of its stable cash flows as dividends (it currently yields more than 4%). Brookfield retains the rest to reinvest in growing its operations. The company also has a strong investment-grade balance sheet to support its dividend and growth. Additionally, Brookfield routinely recycles capital by selling mature assets to fund higher-returning new investments. It focuses on investing in infrastructure benefiting from global megatrends, including digitalization, decarbonization, and deglobalization.

Today's Change

(

-2.06

%) $

-0.85

Current Price

$

40.46

Brookfield's organic growth drivers (inflation-linked rate increases, volume growth as the global economy expands, and expansion projects) should support 6% to 9% annual FFO per share growth. Meanwhile, acquisitions funded through its capital recycling initiatives should boost its growth rate above 10% annually. That supports the company's plan to grow its dividend by 5% to 9% per year. Brookfield has increased its payout every year since its formation 17 years ago, growing it at a 9% compound annual rate.

Powerful growth tailwinds Brookfield Renewable is the renewable energy-focused sibling of Brookfield Infrastructure. It operates one of the world's largest publicly traded renewable power and sustainable solutions platforms. Brookfield Renewable generates stable and growing cash flows backed by long-term contracts (90% of its FFO) that link rates to inflation (70% of its revenue). The company's stable cash flows support its nearly 4%-yielding dividend.

Today's Change

(

0.51

%) $

0.19

Current Price

$

37.68

Inflation-linked rate increases, margin enhancement activities, and development projects should power 8% to 13% annual FFO per share growth over the next five years. Brookfield is currently ramping up its development activities to support surging demand for power by AI data centers and other drivers. Additionally, Brookfield routinely recycles capital to make value-enhancing acquisitions. That drives its view that it can grow FFO per share by more than 10% annually through 2031.

Brookfield Renewable also expects to grow its high-yielding dividend by 5% to 9% each year. It has raised its payout by at least 5% per year since 2011.

Income backed by mission-critical properties W.P. Carey is a real estate investment trust (REIT). It owns a well-diversified portfolio of operationally critical warehouse, industrial, and retail properties across North America and Europe secured by long-term net leases with built-in rent escalations. These properties generate very stable and steadily rising rental income to support the REIT's nearly 5%-yielding dividend.

Today's Change

(

-0.34

%) $

-0.26

Current Price

$

75.58

The REIT's leases deliver low-to-mid single-digit annual rent growth. W.P. Carey complements this growth by investing in additional income-generating properties. It invests in build-to-suit projects, completes sale-leaseback transactions, and buys real estate portfolios from other investors. It funds these new investments with post-dividend free cash flow, non-core property sales, its strong balance sheet, and stock sales.

W.P. Carey has increased its dividend every quarter since resetting the payout in late 2023 following its strategic decision to exit the office sector, including by 4.5% over the past year. Its payout should continue growing at a low-to-mid single-digit rate, roughly matching its adjusted FFO growth rate.

Ideal income investments Brookfield Infrastructure, Brookfield Renewable, and W.P. Carey generate stable and steadily rising cash flows to support their high-yielding dividends. They also have rock-solid financial profiles to drive their continued growth. Their high-yielding and steadily rising payouts will help me achieve financial freedom faster, which is why I can't wait to buy even more shares this June.

Matt DiLallo has positions in Brookfield Infrastructure, Brookfield Infrastructure Partners, Brookfield Renewable, Brookfield Renewable Partners, and W.P. Carey. The Motley Fool recommends Brookfield Infrastructure Partners, Brookfield Renewable, and Brookfield Renewable Partners. The Motley Fool has a disclosure policy.
2026-06-12 11:47 1mo ago
2026-06-04 11:00 1mo ago
Brookfield Renewable Partners Is Up 38% This Year. Does AI Energy Demand Make This Green Energy Stock a Buy in 2026?
BEP Brookfield Renewable Partners
FMP Stock News
Original source text
Renewable energy stocks were supposed to be some of the losers under the second Trump administration. The president is famously not a fan of wind turbines or solar energy. Yet one diversified energy play is having an outstanding year.

Shares of Brookfield Renewable Partners (BEP +0.31%) have soared by 37.5% year to date through May. Here's a look at several reasons investors shouldn't overlook Brookfield Renewable Partners, but also one reason to be wary.

Image source: The Motley Fool.

Brookfield is diversified Brookfield Renewable's underlying business is one of the reasons the stock has performed well so far this year. The company continued its trend of growing funds from operations (FFO), with a 19% year-over-year increase in Q1. The financial measure, commonly used by real estate investment trusts (REITs), defines cash generated from underlying operations and has increased by 12% over the last year versus the prior period.

Connor Teskey, CEO of Brookfield Renewable and president of Brookfield Asset Management, summarized the company's recent success this way:

Growing energy demand is now occurring alongside a renewed focus on energy security. In an environment with strong demand for low-cost, quick-to-market, and increasingly locally sourced energy, we are well positioned to deliver sustainable, long-term cash flow growth for our investors.

Brookfield was poised to capitalize on the growing demand, thanks to its diversification across energy markets and technologies. While a little over half of its assets under management are in North America, the company also has meaningful energy assets in Europe, Latin America, and across the Asia-Pacific region.

Today's Change

(

0.31

%) $

0.11

Current Price

$

35.38

Power production assets are in demand as data centers increase global energy demand and the Strait of Hormuz conflict rattles oil markets. It highlights where Brookfield's expertise makes a difference. The company is a strong capital allocator, and management constantly works to identify its best opportunities. In that vein, Brookfield Renewable announced $3 billion in asset sales in Q1 alone as it recycles capital into projects it believes offer better returns.

BEP or BEPC? The equity is also unique. Brookfield Renewable offers partnership units, but investors can also purchase shares of Brookfield Renewable Corp. (BEPC +0.51%). BEP units and BEPC shares both represent the same underlying business and assets. The former is a limited partnership, while the latter is a corporation.

Owning shares in the partnership can lead to more complex tax paperwork, which turns off some investors. That helps explain the recent pricing deviation. Although they pay the same dividend amount per share/unit, their market prices diverged, resulting in different yields.

Data by YCharts.

The partnership units have been playing catch-up this year, resulting in the outsize return. Investors can choose which to buy based on personal situations and tax preparation concerns. But there is no doubt that the underlying business is strong, and Brookfield is a solid renewable energy dividend stock to own. Just don't expect the pace of returns to mirror what we've seen so far in 2026, as the partnership unit price has now closed the gap.
2026-06-12 11:47 1mo ago
2026-06-06 17:15 1mo ago
Are These 3 Energy Stocks About to Soar as Driving Season Kicks Off in the United States?
BEP Brookfield Renewable Partners
FMP Stock News
Original source text
When investors think about the annual summer driving season, oil and gasoline have historically been the primary focus. This year, oil and gasoline have been headline news daily due to the geopolitical conflict in the Middle East. That's likely to remain the case regardless of how much people drive.

But high energy prices could shift demand, making electricity more important than ever. Three stocks you may want to keep an eye on are NextEra Energy (NEE 0.33%), Constellation Energy (CEG +1.82%), and Brookfield Renewable (BEP +0.31%)(BEPC +0.51%). Here's a primer on each one.

Image source: Getty Images.

The EV fleet is bigger than ever before Normally, driving season is about energy companies like integrated energy giant Chevron (CVX 2.10%) and refiner Valero (VLO 0.93%). Chevron's business spans the entire energy value chain, from producing oil to transporting it and processing it into gasoline and other products. Valero sits at the end of the chain, transforming oil into other products. Energy companies like these will likely see a boost from driving season.

However, the bigger story today is the geopolitical conflict in the Middle East. It is an ongoing event that will likely have far more sway over energy prices and, thus, the performance of energy stocks, than the driving season. However, there's another possible consequence from this conflict.

In early 2026, sales of used electric vehicles (EVs) spiked. One logical reason for that is high energy costs. Meanwhile, the percentage of EVs among all vehicles on the road is roughly 2%. Some might argue that 2% is a tiny number, which it is, but it represents more than 5.5 million vehicles. That's a substantial number on an absolute basis, and with gasoline prices so high, consumers could favor EVs over combustion engine vehicles.

Today's Change

(

-0.33

%) $

-0.28

Current Price

$

84.84

Demand is already high for electricity Potential electricity demand this driving season will add to the demand already coming from data centers and artificial intelligence. The three together are key factors in the expected step change in overall demand, with electricity demand projected to grow by 60% between 2025 and 2045. For reference, demand only grew 9% between 2005 and 2025. Those stats come from NextEra Energy, the world's largest utility. It is also one of the world's largest producers of solar and wind power.

NextEra is set to get even larger, with plans to buy competitor Dominion Energy (D 0.12%). That will expand its geographic reach to four states and set it up for even more rapid long-term growth. If high oil prices lead consumers to use more electricity this driving season, the long-term story could get even better here. In other words, 2026 could be an important inflection point for the business and the stock.

Today's Change

(

1.82

%) $

4.41

Current Price

$

246.71

Nuclear power is also becoming an increasingly important source of electricity. Contract power generator Constellation Energy has one of the largest U.S. fleets of nuclear reactors. It is already seeing increased demand from data centers, and transportation demand could be icing on the cake. Notably, it recently acquired Calpine, a company focused on natural gas power plants. Those often get tapped during peak demand periods, like when it is warm in the summer. If this year's driving season comes with an electric demand spike in transportation, Constellation Energy could be a big near-term beneficiary.

Today's Change

(

0.31

%) $

0.11

Current Price

$

35.38

Increased demand for electricity from transportation will also be a long-term benefit to Brookfield Renewable. This company has a global portfolio of renewable power assets. It sells power under long-term contracts, so there won't likely be a near-term impact on its business. However, if this driving season marks a shift toward electric vehicles, the clean energy Brookfield Renewable provides could become increasingly important globally. That could easily increase the rate at which Brookfield Renewable builds new assets, which investors would likely price into the stock pretty quickly.

This summer could be the leading edge of an important change Electricity is an increasingly important source of energy. When oil prices are low, the transition from carbon energy sources to electricity isn't as pressing. However, with oil prices at lofty levels, electricity looks increasingly attractive. This year's driving season could be an important test.

Constellation Energy is a more growth-oriented story, noting it only has a dividend yield of around 0.6%. However, NextEra Energy's yield is 2.9%, and Brookfield Renewable Partners' yield is 4.2%. Both have solid histories of annual dividend increases, making them attractive to dividend investors.
2026-06-12 11:47 1mo ago
2026-06-08 11:00 1mo ago
Engineered Mineral Hydrogen Emerges as Next Major Energy Disruption Opportunity Amid Explosive Global Demand
BEP Brookfield Renewable Partners
FMP Stock News
Original source text
New breakthroughs in low-cost hydrogen extraction and growing clean energy demand position the sector for significant long-term market expansion

, /PRNewswire/ -- Market News Updates News Commentary - The Engineered Mineral Hydrogen sector is gaining momentum as the demand for cleaner and more cost-effective energy sources grows globally. Unlike traditional hydrogen production methods that heavily depend on natural gas or expensive electrolysis systems, Engineered Mineral Hydrogen harnesses natural chemical reactions between water and iron-rich rocks deep below the surface to generate hydrogen in a more sustainable way. Many companies are now exploring ultramafic rock formations and serpentinization processes as scalable energy solutions, especially in regions rich in nickel and iron reserves. Recent industry advancements, like new partnerships and trial projects in Newfoundland and North America, signify a shift from research to commercial deployment.  Active Companies mentioned in the article includes: First Atlantic Nickel Corp. (OTCQB: FANCF) (TSX-V: FAN), Total Energy Services Inc. (OTC: TOTZF) (TSX: TOT), Exxon Mobil Corporation (NYSE: XOM), Chevron Corporation (NYSE: CVX), Brookfield Renewable Partners L.P. (NYSE: BEP).

One attractive aspect for investors in this field is the potential cost-effectiveness. Experts believe that engineered or natural hydrogen could eventually become one of the most cost-efficient forms of clean hydrogen due to the earth's natural gas production capabilities, reducing the need for extensive industrial energy inputs. The global hydrogen market is expected to see significant growth, reaching approximately $66.5 billion by 2034 from $21.7 billion in 2026, driven by increasing industrial demand, transportation, AI-driven data centers, and energy storage applications. Simultaneously, the emerging natural and engineered hydrogen sector is projected to experience even faster growth, with market analyses suggesting that the natural hydrogen market could surge from about $158 million in 2025 to over $2.2 billion by 2032.

The excitement surrounding Engineered Mineral Hydrogen is fueled by rising concerns over energy security and growing interest in low-carbon industrial fuels. Companies are increasingly looking for reliable domestic energy sources to reduce dependence on imported fuels while supporting decarbonization efforts. Analysts predict a notable increase in drilling projects, pilot installations, and long-term contracts beyond 2026 as the sector develops. Although still in its early stages and carrying exploration risks similar to mining or oil exploration, many investors see it as a disruptive opportunity within the broader clean energy market landscape. If commercial-scale production proves successful, Engineered Mineral Hydrogen has the potential to play a crucial role in the global energy mix in the next decade.

Vema Hydrogen and First Atlantic Nickel & Cobalt Sign LOI to Develop Engineered Mineral Hydrogen at Pipestone XL Awaruite Project in Newfoundland 

Vema's Engineered Mineral Hydrogen could supply regional industry and seaborne export markets from the Pipestone XL Project in central Newfoundland. The Pipestone Ophiolite Complex spans 30 kilometers of ultramafic rock, and holds enough potential hydrogen to power industrial demand in Newfoundland for generations Vema Hydrogen ("Vema") today announced that it has entered into a non-binding Letter of Intent (the "LOI") with First Atlantic Nickel & Cobalt Corp (TSXV: FAN) (OTCQB: FANCF) (FSE: P21) ("First Atlantic"), to jointly develop Engineered Mineral Hydrogen, or EMH, at the Pipestone XL project, a 30-kilometer ultramafic belt in central Newfoundland. Under the LOI, the parties intend to establish a 50/50 joint venture to produce low-carbon hydrogen alongside First Atlantic's primary awaruite nickel-cobalt program. The partnership is intended to serve as a first-of-its-kind template for combining hydrogen production with critical mineral development at ultramafic sites, with the potential to attract co-located investment in clean fuels, ammonia, and downstream industry.

"Vema's Engineered Mineral Hydrogen is on the verge of delivering clean energy at a scale cost-competitive with hydrocarbons," said Dr. Douglas Wicks, Strategic Advisor to First Atlantic & Cobalt and former Program Director for ARPA-E's MINER program and Geologic Hydrogen portfolio. "Awaruite forms through serpentinization when hydrogen reduces nickel and iron, so its presence at Pipestone XL is a clear signature of a hydrogen-rich system. Vema's technology could engineer that same reaction for hydrogen production, and Pipestone XL is an ideal location due to its size, proximity to infrastructure, and the potential for cost efficiencies in co-locating hydrogen production with nickel & cobalt mining. Having worked closely with Vema's founders since before the company's founding — and having seen firsthand how they developed the engineered approach to geologic hydrogen — I believe Pipestone XL represents a compelling opportunity to bring this technology to commercial scale."

Over the past twelve months, Vema has worked with First Atlantic to evaluate the Pipestone Ophiolite Complex, analyzing geological and geophysical data as well as infrastructure across the 30-kilometer belt. Laboratory testing of Pipestone rock samples at Vema's Orléans facility in France confirmed hydrogen production through stimulated serpentinization, indicating that the formation is well suited to EMH. Vema will leverage the experience gained in its established site in the Thetford ophiolite in Quebec, where Vema operates the world's first Engineered Mineral Hydrogen project.

Newfoundland is a significant region for critical minerals and clean energy development, but exploration and mining remain energy-intensive. Engineered Mineral Hydrogen (EMH) produces hydrogen from iron-rich rock through naturally occurring geochemical reactions, with no grid electricity required. Locally produced hydrogen at Pipestone could, over time, support on-site energy needs for a large-scale nickel and cobalt mining district and related downstream industries.

"Vema operates the world's first Engineered Mineral Hydrogen project at the Thetford ophiolite in Quebec. Rock samples collected during Vema's site visit to Pipestone XL were tested at their lab in Orléans, France, confirming the hydrogen generation potential of the ultramafic host rocks. Given the link between awaruite formation and hydrogen, we're excited about the potential for Vema's technology to maximize the value of our unique nickel-cobalt alloy project," said Adrian Smith, P.Geo., CEO of First Atlantic.

The collaboration also positions both companies to explore how locally produced hydrogen could reshape energy planning for remote industrial sites. By pairing EMH supply with critical mineral development, the partners aim to demonstrate a model that strengthens regional energy resilience while reducing reliance on long-distance fuel transport.

"Engineered Mineral Hydrogen is a promising new primary energy source for regions with iron-rich rock, like at Pipestone," said Pierre Levin, CEO and Co-Founder of Vema Hydrogen. "Now with validated rock samples and permitting in place, we have a clear path to advance EMH at Pipestone and to expand the model across North America."

Awaruite (Ni₃Fe) is a naturally occurring, magnetic nickel-iron-cobalt alloy (Ni-Fe-Co). The U.S. Geological Survey has identified awaruite as a potential solution to nickel concentrate shortages, noting that it is much easier to concentrate than pentlandite, the principal nickel sulphide. Its magnetic, metallic nature allows recovery by both magnetic separation and flotation, without the smelting, roasting, or acid leaching that conventional nickel ores require.  CONTINUED… Read this and more news for First Atlantic Nickel at:  https://www.fanickel.com/archive

In other market news of interest today includes:

Total Energy Services Inc. (OTC: TOTZF) (TSX:TOT) recently announced its consolidated financial results for the three months ended March 31, 2026.

Total Energy's results for the three months ended March 31, 2026 reflect continued strong North American demand for natural gas compression and process equipment and the deployment of upgraded drilling and service rigs in Australia and Canada that more than offset a year over year decline in North American drilling and completion activity. Negatively impacting first quarter financial results was a $6.5 million year over year increase in share-based compensation expense due to the 52% increase in the Company's share price during the first quarter of 2026. This was partially offset by a $2.9 million year over year increase on the gain on sale of property, plant and equipment following the sale of certain well servicing equipment in the United States in February 2026.

Exxon Mobil Corporation (NYSE: XOM) recently announced its Board of Directors has unanimously recommended shareholders approve changing the company's legal domicile from New Jersey to Texas. The Board concluded that aligning ExxonMobil's legal domicile with where its leadership and core operations have been based since 1989 will benefit shareholders.

"Over the past several years, Texas has made a noticeable effort to embrace the business community. In doing so, it has created a policy and regulatory environment that can allow the company to maximize shareholder value," said Darren Woods, ExxonMobil chairman and chief executive officer. "Aligning our legal home with our operating home, in a state that understands our business and has a stake in the company's success, is important."

In making its recommendation, the Board considered Texas' legal and regulatory environment, including its modernized business statutes and the Texas Business Court, which is designed to resolve complex disputes efficiently. When corporate decisions are challenged, Texas courts are required to apply clear, statute based standards, which support sound decision-making.

Chevron U.S.A. Inc., a subsidiary of Chevron Corporation (NYSE: CVX), recently announced the introduction of next-generation Techron®, a reformulated version of its proprietary gasoline additive designed to provide greater protection for engines from harmful deposits caused by lower quality fuels, supporting long-term engine performance.

Techron has been trusted by drivers for decades as part of Chevron- and Texaco-branded gasolines. The latest reformulation reflects Chevron's continued investment in fuel quality and scientific testing to help ensure its fuels meet the needs of today's engines and driving conditions.

"Fuel technology never stands still," said Andy Walz, president, Chevron Downstream, Midstream and Chemicals. "This new Techron formulation builds on what drivers already expect from our branded fuels – clean engines, reliable performance and confidence at the pump – while reinforcing our continued focus on science based innovation."

Brookfield Renewable Partners L.P. (NYSE: BEP) recently reported financial results for the three months ended March 31, 2026.

"We had a strong start to the year, delivering record financial results, advancing our growth priorities and strengthening our balance sheet. The quarter was highlighted by our acquisition of Boralex, a global, listed renewable platform with a significant operating base and a large, de-risked development pipeline that complements our existing business and where we are uniquely positioned to accelerate growth and create value," said Connor Teskey, CEO of Brookfield Renewable.

He added, "We also continue to increase our development activities, advance key workstreams to support new nuclear deployment at Westinghouse, and scale our capital recycling strategy, agreeing to sell nearly $3 billion of assets this quarter alone. Growing energy demand is now occurring alongside a renewed focus on energy security. In an environment with strong demand for low-cost, quick to market, and increasingly locally sourced energy, we are well positioned to deliver sustainable long-term cash flow growth for our investors."

DISCLAIMER: MarketNewsUpdates.com (MNU) is a third party publisher and news dissemination service provider, which disseminates electronic information through multiple online media channels. MNU is NOT affiliated in any manner with any company mentioned herein. MNU and its affiliated companies are a news dissemination solutions provider and are NOT a registered broker/dealer/analyst/adviser, holds no investment licenses and may NOT sell, offer to sell or offer to buy any security. MNU'S market updates, news alerts and corporate profiles are NOT a solicitation or recommendation to buy, sell or hold securities. The material in this release is intended to be strictly informational and is NEVER to be construed or interpreted as research material. All readers are strongly urged to perform research and due diligence on their own and consult a licensed financial professional before considering any level of investing in stocks.  All material included herein is republished content and details which were previously disseminated by the companies mentioned in this release. MNU is not liable for any investment decisions by its readers or subscribers. Investors are cautioned that they may lose all or a portion of their investment when investing in stocks. This press release was distributed on behalf of First Atlantic Nickel Corp. For current services performed MNU has been compensated twenty five hundred dollars for news coverage of the current press releases issued by First Atlantic Nickel Corp. by a non-affiliated third party. FNM & MNU HOLD NO SHARES OF ANY COMPANY NAMED IN THIS RELEASE.

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SOURCE Market News Updates
2026-06-12 11:47 1mo ago
2026-04-02 05:00 3mo ago
Roivant Announces Expansion of Brepocitinib Development Program with New Phase 2b/3 Trial in Lichen Planopilaris (LPP) and Phase 3 Study Results for Batoclimab in Thyroid Eye Disease (TED)
ROIV Roivant Sciences
FMP Stock News
Original source text
April 02, 2026 05:00 ET  | Source: Roivant Sciences

Lichen planopilaris (LPP) is a highly morbid inflammatory scalp disorder that causes generally irreversible scarring hair loss, often accompanied by profound pain, itch, and burning sensations; no FDA-approved therapies exist for LPP, highlighting a critical unmet therapeutic needLPP marks the fourth indication in brepocitinib’s expanding late-stage development programMultiple lines of evidence, including strong mechanistic rationale and clinically meaningful results in an investigator-initiated placebo-controlled study of brepocitinib in LPP, support rapid development of brepocitinib in this indicationA seamless Phase 2b/3 potentially registrational trial of brepocitinib in LPP enrolled its first subjects in March 2026Immunovant’s Phase 3 studies of batoclimab in thyroid eye disease (TED) each failed to meet their primary endpoint; safety results were consistent with previous findingsPatients in the TED studies demonstrated greater levels of proptosis improvement from baseline after the initial 12-week high-dose period than after the following 12-week low-dose period, supporting the benefit of deeper IgG suppression. The hyperthyroid patients in the TED studies showed similar response rates of thyroid hormone normalization to those seen in the batoclimab Phase 2 study in Graves’ diseaseImmunovant remains focused on rapid advancement of IMVT-1402 in multiple indicationsRoivant will host an investor call to discuss these updates today, April 2, 2026, at 8:00 a.m. ET BASEL, Switzerland and LONDON and NEW YORK, April 02, 2026 (GLOBE NEWSWIRE) -- Roivant (Nasdaq: ROIV) today announced a new Phase 2b/3 clinical program for brepocitinib in lichen planopilaris (LPP), a highly morbid inflammatory scalp disorder affecting approximately 100,000 adults in the United States, and reported the topline results from Immunovant’s two Phase 3 (GO) clinical studies evaluating batoclimab as an investigational treatment for adults with active, moderate-to-severe thyroid eye disease (TED).

Brepocitinib in LPP

LPP inflammation targets the stem cell-rich bulge region of the hair follicle (the permanent portion responsible for hair growth), resulting in generally irreversible hair loss and permanent scarring. LPP is also associated with other burdensome symptoms, including pain, burning, itching, and scaling and an increased risk of comorbidities such as other autoimmune diseases and skin cancers. There are currently no FDA-approved therapies to treat LPP.

“Lichen planopilaris (LPP) is what my colleagues and I refer to as a ‘trichologic emergency,’” said Dr. Kristen Lo Sicco, Chief of the Skin and Cancer Unit at NYU Langone Health, Board Member of the Scarring Alopecia Foundation, and Associate Professor of Dermatology at the Ronald O. Perelman Department of Dermatology at NYU Grossman School of Medicine. “Absent early diagnosis and aggressive intervention, patients experience rapid hair loss that is generally irreversible, leaves permanent scarring, and is often accompanied by erythema, scaling, pain, itching and burning sensations. Untreated LPP also leads to increased risk of skin cancers and other comorbidities. Efficacious FDA-approved treatments are urgently needed.”

Priovant recently began enrolling subjects in a seamless Phase 2b/3 study of brepocitinib in LPP, with the first subjects enrolled in March 2026. This program marks Priovant’s fourth indication in late-stage clinical development, alongside dermatomyositis (DM), non-infectious uveitis (NIU) and cutaneous sarcoidosis (CS). The U.S. Food and Drug Administration (FDA) recently granted Priority Review to brepocitinib’s New Drug Application (NDA) for DM and assigned a Prescription Drug User Fee Act (PDUFA) target action date in the third quarter of calendar year 2026. Topline Phase 3 data in NIU and Phase 3 study initiation in CS are expected in the second half of calendar year 2026.

“Expanding brepocitinib into lichen planopilaris continues our strategy of developing brepocitinib in highly morbid orphan conditions with limited treatment options and distinctive mechanistic benefits of dual JAK1/TYK2 inhibition,” said Ben Zimmer, Priovant CEO. “Moreover, as we look ahead to our expected product launch in DM in September, we see LPP as a strategic fit into a multi-indication rheum-derm rare disease franchise anchored by DM, with overlapping prescriber bases and thought leaders.”

Immunovant Phase 3 Studies in TED

Based on the pre-specified statistical analysis plan, the studies failed to meet their primary endpoint of ≥2mm proptosis responder rate at Week 24, following 12 weeks of high-dose and 12 weeks of low-dose batoclimab treatment. Safety results were consistent with previous findings, and no new safety signals were identified.

Patients in the TED studies had greater levels of proptosis improvement from baseline after the initial 12-week high-dose period than after the following 12-week low-dose period, supporting the benefit of deeper IgG suppression.

The subset of hyperthyroid patients in the TED studies showed similar response rates of thyroid hormone normalization to those seen in the batoclimab Phase 2 study in Graves’ disease.

Immunovant remains focused on rapidly advancing the clinical development of IMVT-1402, an investigational FcRn blocker, across multiple autoimmune diseases with significant unmet need, with Graves’ disease as a key strategic priority. Recent Phase 2 proof-of-concept data highlighted FcRn blockade as a potentially disease-modifying approach in Graves’ disease. Topline data from the potentially registrational studies of IMVT-1402 in Graves’ disease are expected in calendar year 2027.

Immunovant intends to review future plans for the development of batoclimab with its partner HanAll Biopharma Co., Ltd. (HanAll) and to provide an update on the program, in conjunction with HanAll, at a future date.

Investor Conference Call Information

Roivant will host a live conference call and webcast at 8:00 a.m. ET on Thursday, April 2, 2026, to discuss these updates.

To access the conference call by phone, please register online using this registration link. The presentation and webcast details will also be available under “Events & Presentations” in the Investors section of the Roivant website at https://investor.roivant.com/news-events/events. The archived webcast will be available on Roivant’s website after the conference call.

About Roivant

Roivant (Nasdaq: ROIV) is a biopharmaceutical company that aims to improve the lives of patients by accelerating the development and commercialization of medicines that matter. Roivant’s pipeline includes brepocitinib, a potent small molecule inhibitor of JAK1 and TYK2 in development for the treatment of dermatomyositis, non-infectious uveitis, cutaneous sarcoidosis and lichen planopilaris; IMVT-1402 and batoclimab, fully human monoclonal antibodies targeting FcRn in development across several IgG-mediated autoimmune indications; and mosliciguat, an inhaled sGC activator in development for pulmonary hypertension associated with interstitial lung disease. We advance our pipeline by creating nimble subsidiaries or “Vants” to develop and commercialize our medicines and technologies. Beyond therapeutics, Roivant also incubates discovery-stage companies and health technology startups complementary to its biopharmaceutical business. For more information, visit https://roivant.com.

Roivant Forward-Looking Statements

This press release contains forward-looking statements. Statements in this press release may include statements that are not historical facts and are considered forward-looking within the meaning of Section 27A of the Securities Act of 1933, as amended (the “Securities Act”), and Section 21E of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), which are usually identified by the use of words such as “anticipate,” “believe,” “continue,” “could,” “estimate,” “expect,” “intends,” “may,” “might,” “plan,” “possible,” “potential,” “predict,” “project,” “should,” “would” and variations of such words or similar expressions. The words may identify forward-looking statements, but the absence of these words does not mean that a statement is not forward-looking. We intend these forward-looking statements to be covered by the safe harbor provisions for forward-looking statements contained in Section 27A of the Securities Act and Section 21E of the Exchange Act.

Our forward-looking statements include, but are not limited to, statements regarding our or our management team’s expectations, hopes, beliefs, intentions or strategies regarding the future, and statements that are not historical facts, including statements about the clinical and therapeutic potential of our product candidates, the availability and success of topline results from our ongoing clinical trials and any commercial potential of our product candidates following applicable regulatory approvals. In addition, any statements that refer to projections, forecasts or other characterizations of future events, results or circumstances, including any underlying assumptions, are forward-looking statements. Actual results may differ materially from those contemplated in these statements due to a variety of risks, uncertainties and other factors.

Although we believe that our plans, intentions, expectations and strategies as reflected in or suggested by those forward-looking statements are reasonable, we can give no assurance that the plans, intentions, expectations or strategies will be attained or achieved. Furthermore, actual results may differ materially from those described in the forward-looking statements and will be affected by a number of risks, uncertainties and assumptions, including, but not limited to, those risks set forth in the Risk Factors section of our filings with the U.S. Securities and Exchange Commission. Moreover, we operate in a very competitive and rapidly changing environment in which new risks emerge from time to time. These forward-looking statements are based upon the current expectations and beliefs of our management as of the date of this press release, and are subject to certain risks and uncertainties that could cause actual results to differ materially from those described in the forward-looking statements. Except as required by applicable law, we assume no obligation to update publicly any forward-looking statements, whether as a result of new information, future events or otherwise.

Contacts:

Investors

Keyur Parekh

[email protected]

Media

Stephanie Lee

[email protected]
2026-06-12 11:47 1mo ago
2026-04-02 16:32 3mo ago
Roivant Sciences Ltd. (ROIV) Discusses Brepocitinib Program Expansion and Phase III Batoclimab Data Update Transcript
ROIV Roivant Sciences
FMP Stock News
Original source text
Roivant Sciences Ltd. (ROIV) Discusses Brepocitinib Program Expansion and Phase III Batoclimab Data Update Transcript
2026-06-12 11:47 1mo ago
2026-04-04 01:05 3mo ago
Roivant Sciences Adds Brepocitinib LPP Trial as Batoclimab Misses Phase III TED Endpoint
ROIV Roivant Sciences
FMP Stock News
Original source text
Roivant Sciences (NASDAQ:ROIV) outlined plans to expand development of its JAK1/TYK2 inhibitor brepocitinib into lichen planopilaris (LPP) and provided an update on a Phase III thyroid eye disease (TED) trial for batoclimab during a conference call hosted by the company.

Brepocitinib expands into lichen planopilaris Roivant CEO Matt Gline said the company is moving “with urgency” to broaden brepocitinib across multiple indications, focusing on orphan immunology diseases with high unmet need, aligned biology for dual JAK1/TYK2 inhibition, and limited or no approved options. Alongside existing programs in dermatomyositis, non-infectious uveitis, and cutaneous sarcoidosis, Gline announced LPP as a new addition, describing it as “a fourth leg to the stool.”

Gline characterized LPP as a “severe and deeply unpleasant disease,” describing it as a highly morbid inflammatory scalp disorder that targets the permanent portion of the hair follicle, leading to generally irreversible hair loss and scarring that “can be permanently disfiguring.” He also cited intense symptoms including pain, itch, burning, redness, and scaling. He said there are no FDA-approved therapies and that patients often require chronic, aggressive, multimodal treatment that is frequently poorly effective.

Management noted the company views LPP as an “orphan-sized” opportunity, with Gline estimating “probably up to 100,000 U.S. patients,” and said the literature suggests prevalence and diagnosis are increasing over time.

Priovant details disease burden and biological rationale Ben Zimmer, CEO of Priovant, said LPP carries substantial burden beyond scalp symptoms, citing an association with increased risk of severe comorbidities, “including both skin cancer and other autoimmune diseases.” He added that clinicians often attempt multiple off-label therapies but that outcomes are limited and discontinuations are common due to tolerability and efficacy.

Zimmer said Priovant believes brepocitinib is well matched to LPP biology, describing the condition as driven primarily by “Th1 polarized T cell aberrant behavior.” He noted that interferon gamma and IL-12 are critical Th1 cytokines and that a JAK1/TYK2 inhibitor can suppress signaling of both. Zimmer pointed to experience in cutaneous sarcoidosis—another Th1-driven condition studied with brepocitinib—as supportive of the mechanistic fit.

Zimmer also referenced case reports and investigator-initiated studies of JAK1 and TYK2 inhibitors as clinical validation for the mechanism. He discussed a small, placebo-controlled investigator-initiated trial at Mount Sinai that used the LPPAI endpoint, which he described as “a generally noisy instrument” that is not preferred by clinicians. While urging caution about overinterpreting a small dataset, Zimmer said the broader takeaway supported proof-of-concept and helped underpin the company’s decision to move quickly.

Zimmer emphasized biomarker findings from that study, saying the “most powerful” aspect was evidence of brepocitinib activity on multiple markers of Th1-driven inflammation, including interferon gamma, IL-12, and chemokines such as CCL5.

Combined Phase IIb/III trial underway; IGA endpoint planned Gline said the LPP program has effectively begun as a “direct to registrational combined Phase IIb/III program,” with the study getting underway “last month.” He described a 72-patient Phase IIb portion that will transition immediately into a pivotal Phase III portion under a largely continuous design. The Phase III sample size is expected to be approximately 270 patients, with a sample size re-estimation after Phase IIb.

Management said the design is intended to support endpoint validation and regulatory alignment, while maintaining a pace closer to a straight-to-registrational program. Gline said the company is not yet providing enrollment timeline guidance but noted enthusiasm from investigators and patient communities.

On endpoints, Zimmer said Priovant is using a more structured approach than LPPAI. He described LPPAI as a composite measure with both physician-assessed and patient-reported components, but with limited definitions for raters. The company’s approach will include an investigator global assessment (IGA) focused on erythema and scale using defined criteria, with secondary endpoints to measure symptoms such as pain and itch using numerical rating scales.

In Q&A, Gline and Zimmer indicated the Phase IIb primary endpoint is expected to be an IGA 0/1 response with a two-point reduction, and said they expect—though cannot fully confirm until FDA discussions after Phase IIb—that the Phase III primary endpoint will match. Zimmer noted that placebo rates for rigorous IGA endpoints in inflammatory skin disorders tend to be low, particularly when requiring improvement to 0/1.

On background therapies, Gline said medications were washed out pre-baseline in the Mount Sinai investigator-initiated trial and highlighted that LPP patients often have polypharmacy. Zimmer said the registrational program plans to wash patients out of background medications “quite aggressively,” consistent with Priovant’s approach in other trials.

Batoclimab Phase III TED trial misses primary endpoint; Graves’ signals discussed Gline also addressed topline Phase III results in TED for batoclimab, Immunovant’s first-generation anti-FcRn antibody, stating the studies “failed to meet their primary endpoint.” He said the TED program was effectively the last readout for the first-generation molecule, with future development focused on IMVT-1402.

The TED primary endpoint was a ≥2 mm proptosis responder rate, which the trial did not achieve. Gline said the company is not pursuing further progress in TED with batoclimab, while noting the dataset provided scientific insights. He described the trial design as 12 weeks of high-dose batoclimab aimed at deep IgG suppression followed by 12 weeks of lower dosing. He said performance was generally better during the initial 12-week high-dose period than during the subsequent lower-dose period, a pattern he said was consistent across endpoints.

Gline said the trial showed “meaningful numerical separation” from placebo on change in proptosis at week 12, and noted that when pooling two TED studies, that measure was “nominally significant” in a post-hoc analysis, while emphasizing the limitations of such analyses. He added that proptosis improvements diminished between weeks 12 and 24 after dose reduction.

Management also highlighted results in a small subset of hyperthyroid patients included within TED enrollment criteria. Gline said there were about 20 hyperthyroid patients across active treatment arms in the pooled dataset. He reported a 75% mean IgG reduction and an 80% responder rate by a thyroid hormone definition (T3 and T4 below the upper limit of normal without increased antithyroid drug dosing), which he said matched the responder rate observed in a prior Phase II Graves’ study at week 12. He also said responder rates declined in the second 12-week period as IgG suppression lessened.

In response to analyst questions, Gline said hyperthyroid patients in the TED studies performed “somewhat better” on proptosis than the overall TED population. He also noted that antithyroid drug dose titration was not allowed in TED, limiting insight into real-world dose adjustments in that setting.

Gline said enrollment in the ongoing IMVT-1402 Graves’ program is “going well,” and reiterated expectations that both Graves’ studies will read out next year. He noted the Graves’ program excludes moderate to severe TED patients and is focused on endocrinology-driven sites, though the company expects to assess ocular symptom outcomes in Graves’ as well.

About Roivant Sciences (NASDAQ:ROIV) Roivant Sciences is a biopharmaceutical company focused on the development and commercialization of innovative therapies through a network of subsidiary businesses known as “Vants.” Founded in 2014, Roivant acquires or in-licenses clinical-stage assets that have progressed beyond proof of concept and seeks to advance them efficiently toward regulatory approval. By organizing each program into a dedicated subsidiary, the company aims to streamline decision-making, allocate resources more effectively, and accelerate development timelines.

The core activities of Roivant involve identifying promising drug candidates across a range of therapeutic areas, including neurology, rare diseases, immunology, oncology, and women’s health.

Featured Stories Five stocks we like better than Roivant Sciences
2026-06-12 11:47 1mo ago
2026-04-06 04:43 3mo ago
Capricorn Fund Managers Ltd Buys 247,000 Shares of Roivant Sciences Ltd. $ROIV
ROIV Roivant Sciences
FMP Stock News
Original source text
Posted by Defense World Staff on Apr 6th, 2026

Capricorn Fund Managers Ltd raised its stake in Roivant Sciences Ltd. (NASDAQ:ROIV – Free Report) by 124.4% during the 4th quarter, according to its most recent Form 13F filing with the Securities and Exchange Commission. The firm owned 445,500 shares of the company’s stock after buying an additional 247,000 shares during the quarter. Roivant Sciences accounts for about 2.3% of Capricorn Fund Managers Ltd’s portfolio, making the stock its 11th largest position. Capricorn Fund Managers Ltd owned approximately 0.06% of Roivant Sciences worth $9,667,000 as of its most recent filing with the Securities and Exchange Commission.

Other institutional investors also recently modified their holdings of the company. Jones Financial Companies Lllp raised its position in shares of Roivant Sciences by 226.0% in the 3rd quarter. Jones Financial Companies Lllp now owns 1,656 shares of the company’s stock valued at $25,000 after acquiring an additional 1,148 shares during the period. Allworth Financial LP grew its holdings in Roivant Sciences by 48.1% during the third quarter. Allworth Financial LP now owns 1,795 shares of the company’s stock valued at $27,000 after purchasing an additional 583 shares during the period. Bessemer Group Inc. grew its holdings in Roivant Sciences by 41.5% during the third quarter. Bessemer Group Inc. now owns 1,852 shares of the company’s stock valued at $28,000 after purchasing an additional 543 shares during the period. Osaic Holdings Inc. increased its stake in Roivant Sciences by 204.2% in the second quarter. Osaic Holdings Inc. now owns 5,783 shares of the company’s stock valued at $65,000 after purchasing an additional 3,882 shares in the last quarter. Finally, Aster Capital Management DIFC Ltd increased its stake in Roivant Sciences by 75.8% in the third quarter. Aster Capital Management DIFC Ltd now owns 4,405 shares of the company’s stock valued at $67,000 after purchasing an additional 1,900 shares in the last quarter. 64.76% of the stock is currently owned by institutional investors and hedge funds.

Analysts Set New Price Targets A number of equities analysts have recently weighed in on the stock. Citigroup lifted their price target on shares of Roivant Sciences from $26.00 to $35.00 and gave the stock a “buy” rating in a research report on Tuesday, February 10th. Sanford C. Bernstein assumed coverage on Roivant Sciences in a research note on Friday, March 20th. They set an “outperform” rating and a $35.00 price objective on the stock. Guggenheim lifted their target price on Roivant Sciences from $28.00 to $30.00 and gave the stock a “buy” rating in a report on Monday, February 9th. Jefferies Financial Group reissued a “buy” rating on shares of Roivant Sciences in a research note on Tuesday, March 3rd. Finally, The Goldman Sachs Group increased their price target on Roivant Sciences from $24.00 to $33.00 and gave the stock a “buy” rating in a report on Monday, December 15th. Nine investment analysts have rated the stock with a Buy rating, one has issued a Hold rating and one has assigned a Sell rating to the stock. According to data from MarketBeat, the company has a consensus rating of “Moderate Buy” and an average target price of $29.50.

Get Our Latest Report on ROIV

Roivant Sciences Price Performance Roivant Sciences stock opened at $28.33 on Monday. The company has a 50 day moving average of $26.80 and a 200-day moving average of $22.28. Roivant Sciences Ltd. has a twelve month low of $8.73 and a twelve month high of $30.33. The stock has a market capitalization of $20.28 billion, a PE ratio of -24.21 and a beta of 1.20.

Insider Transactions at Roivant Sciences In other news, Director Daniel Allen Gold sold 425,000 shares of the business’s stock in a transaction dated Wednesday, February 11th. The stock was sold at an average price of $26.67, for a total value of $11,334,750.00. Following the sale, the director directly owned 15,928,113 shares in the company, valued at $424,802,773.71. The trade was a 2.60% decrease in their ownership of the stock. The sale was disclosed in a document filed with the SEC, which is available at the SEC website. Also, Director Melissa B. Epperly sold 41,861 shares of the company’s stock in a transaction dated Monday, March 16th. The stock was sold at an average price of $28.68, for a total value of $1,200,573.48. Following the transaction, the director directly owned 15,804 shares of the company’s stock, valued at $453,258.72. This represents a 72.59% decrease in their ownership of the stock. The disclosure for this sale is available in the SEC filing. In the last 90 days, insiders sold 4,782,086 shares of company stock worth $128,848,063. Company insiders own 10.80% of the company’s stock.

About Roivant Sciences (Free Report)

Roivant Sciences is a biopharmaceutical company focused on the development and commercialization of innovative therapies through a network of subsidiary businesses known as “Vants.” Founded in 2014, Roivant acquires or in-licenses clinical-stage assets that have progressed beyond proof of concept and seeks to advance them efficiently toward regulatory approval. By organizing each program into a dedicated subsidiary, the company aims to streamline decision-making, allocate resources more effectively, and accelerate development timelines.

The core activities of Roivant involve identifying promising drug candidates across a range of therapeutic areas, including neurology, rare diseases, immunology, oncology, and women’s health.

Further Reading Five stocks we like better than Roivant Sciences

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2026-06-12 11:47 1mo ago
2026-04-10 13:00 3mo ago
Montes Archimedes Acquisition (ROIV) Upgraded to Buy: Here's What You Should Know
ROIV Roivant Sciences
FMP Stock News
Original source text
Investors might want to bet on Roivant Sciences Ltd. (ROIV - Free Report) , as it has been recently upgraded to a Zacks Rank #2 (Buy). An upward trend in earnings estimates -- one of the most powerful forces impacting stock prices -- has triggered this rating change.

The sole determinant of the Zacks rating is a company's changing earnings picture. The Zacks Consensus Estimate -- the consensus of EPS estimates from the sell-side analysts covering the stock -- for the current and following years is tracked by the system.

Individual investors often find it hard to make decisions based on rating upgrades by Wall Street analysts, since these are mostly driven by subjective factors that are hard to see and measure in real time. In these situations, the Zacks rating system comes in handy because of the power of a changing earnings picture in determining near-term stock price movements.

As such, the Zacks rating upgrade for Montes Archimedes Acquisition is essentially a positive comment on its earnings outlook that could have a favorable impact on its stock price.

Most Powerful Force Impacting Stock PricesThe change in a company's future earnings potential, as reflected in earnings estimate revisions, has proven to be strongly correlated with the near-term price movement of its stock. That's partly because of the influence of institutional investors that use earnings and earnings estimates for calculating the fair value of a company's shares. An increase or decrease in earnings estimates in their valuation models simply results in higher or lower fair value for a stock, and institutional investors typically buy or sell it. Their bulk investment action then leads to price movement for the stock.

For Montes Archimedes Acquisition, rising earnings estimates and the consequent rating upgrade fundamentally mean an improvement in the company's underlying business. And investors' appreciation of this improving business trend should push the stock higher.

Harnessing the Power of Earnings Estimate RevisionsEmpirical research shows a strong correlation between trends in earnings estimate revisions and near-term stock movements, so it could be truly rewarding if such revisions are tracked for making an investment decision. Here is where the tried-and-tested Zacks Rank stock-rating system plays an important role, as it effectively harnesses the power of earnings estimate revisions.

The Zacks Rank stock-rating system, which uses four factors related to earnings estimates to classify stocks into five groups, ranging from Zacks Rank #1 (Strong Buy) to Zacks Rank #5 (Strong Sell), has an impressive externally-audited track record, with Zacks Rank #1 stocks generating an average annual return of +25% since 1988. You can see the complete list of today's Zacks #1 Rank (Strong Buy) stocks here >>>> .

Earnings Estimate Revisions for Montes Archimedes AcquisitionThis company is expected to earn -$1.07 per share for the fiscal year ending March 2026, which represents no year-over-year change.

Analysts have been steadily raising their estimates for Montes Archimedes Acquisition. Over the past three months, the Zacks Consensus Estimate for the company has increased 7.4%.

Bottom LineUnlike the overly optimistic Wall Street analysts whose rating systems tend to be weighted toward favorable recommendations, the Zacks rating system maintains an equal proportion of "buy" and "sell" ratings for its entire universe of more than 4,000 stocks at any point in time. Irrespective of market conditions, only the top 5% of the Zacks-covered stocks get a "Strong Buy" rating and the next 15% get a "Buy" rating. So, the placement of a stock in the top 20% of the Zacks-covered stocks indicates its superior earnings estimate revision feature, making it a solid candidate for producing market-beating returns in the near term.

You can learn more about the Zacks Rank here >>>

The upgrade of Montes Archimedes Acquisition to a Zacks Rank #2 positions it in the top 20% of the Zacks-covered stocks in terms of estimate revisions, implying that the stock might move higher in the near term.
2026-06-12 11:47 1mo ago
2026-04-12 04:20 3mo ago
Elevate Capital Advisors LLC Sells 36,236 Shares of Roivant Sciences Ltd. $ROIV
ROIV Roivant Sciences
FMP Stock News
Original source text
Posted by Defense World Staff on Apr 12th, 2026

Elevate Capital Advisors LLC cut its stake in shares of Roivant Sciences Ltd. (NASDAQ:ROIV – Free Report) by 31.8% during the 4th quarter, according to its most recent 13F filing with the Securities and Exchange Commission. The fund owned 77,545 shares of the company’s stock after selling 36,236 shares during the quarter. Elevate Capital Advisors LLC’s holdings in Roivant Sciences were worth $1,683,000 as of its most recent filing with the Securities and Exchange Commission.

Several other hedge funds and other institutional investors also recently made changes to their positions in ROIV. Assenagon Asset Management S.A. grew its holdings in shares of Roivant Sciences by 11,507.5% during the 4th quarter. Assenagon Asset Management S.A. now owns 6,937,112 shares of the company’s stock valued at $150,535,000 after purchasing an additional 6,877,348 shares during the last quarter. Perceptive Advisors LLC bought a new stake in shares of Roivant Sciences during the 2nd quarter valued at approximately $37,546,000. Marshall Wace LLP grew its holdings in shares of Roivant Sciences by 316.5% during the 3rd quarter. Marshall Wace LLP now owns 3,978,001 shares of the company’s stock valued at $60,187,000 after purchasing an additional 3,022,851 shares during the last quarter. Orbimed Advisors LLC bought a new stake in shares of Roivant Sciences during the 2nd quarter valued at approximately $31,324,000. Finally, Rubric Capital Management LP grew its holdings in shares of Roivant Sciences by 14.7% during the 2nd quarter. Rubric Capital Management LP now owns 20,370,336 shares of the company’s stock valued at $229,574,000 after purchasing an additional 2,603,260 shares during the last quarter. 64.76% of the stock is owned by institutional investors.

Analyst Ratings Changes Several equities research analysts recently issued reports on the stock. Citigroup lifted their price target on shares of Roivant Sciences from $26.00 to $35.00 and gave the company a “buy” rating in a report on Tuesday, February 10th. Sanford C. Bernstein initiated coverage on shares of Roivant Sciences in a report on Friday, March 20th. They set an “outperform” rating and a $35.00 target price on the stock. Guggenheim boosted their target price on shares of Roivant Sciences from $28.00 to $30.00 and gave the stock a “buy” rating in a report on Monday, February 9th. Leerink Partners boosted their target price on shares of Roivant Sciences from $29.00 to $32.00 and gave the stock an “outperform” rating in a report on Monday, December 15th. Finally, Weiss Ratings lowered shares of Roivant Sciences from a “hold (c-)” rating to a “sell (d)” rating in a report on Monday, February 9th. Nine research analysts have rated the stock with a Buy rating, one has issued a Hold rating and one has issued a Sell rating to the stock. Based on data from MarketBeat.com, the stock currently has a consensus rating of “Moderate Buy” and an average price target of $29.50.

View Our Latest Stock Report on Roivant Sciences

Insider Activity In other news, insider Frank Torti sold 587,390 shares of the business’s stock in a transaction that occurred on Monday, February 23rd. The shares were sold at an average price of $27.51, for a total value of $16,159,098.90. Following the transaction, the insider owned 13,736,547 shares in the company, valued at approximately $377,892,407.97. The trade was a 4.10% decrease in their position. The sale was disclosed in a document filed with the Securities & Exchange Commission, which is accessible through this link. Also, CAO Jennifer Humes sold 13,538 shares of the business’s stock in a transaction that occurred on Wednesday, April 8th. The stock was sold at an average price of $28.37, for a total transaction of $384,073.06. Following the completion of the transaction, the chief accounting officer owned 84,191 shares in the company, valued at $2,388,498.67. This trade represents a 13.85% decrease in their position. Additional details regarding this sale are available in the official SEC disclosure. Over the last ninety days, insiders sold 4,795,624 shares of company stock worth $129,232,136. Company insiders own 10.80% of the company’s stock.

Roivant Sciences Price Performance ROIV opened at $28.21 on Friday. Roivant Sciences Ltd. has a fifty-two week low of $9.57 and a fifty-two week high of $30.33. The firm has a market capitalization of $20.19 billion, a price-to-earnings ratio of -24.11 and a beta of 1.20. The company’s 50 day moving average price is $27.40 and its two-hundred day moving average price is $22.69.

Roivant Sciences Company Profile (Free Report)

Roivant Sciences is a biopharmaceutical company focused on the development and commercialization of innovative therapies through a network of subsidiary businesses known as “Vants.” Founded in 2014, Roivant acquires or in-licenses clinical-stage assets that have progressed beyond proof of concept and seeks to advance them efficiently toward regulatory approval. By organizing each program into a dedicated subsidiary, the company aims to streamline decision-making, allocate resources more effectively, and accelerate development timelines.

The core activities of Roivant involve identifying promising drug candidates across a range of therapeutic areas, including neurology, rare diseases, immunology, oncology, and women’s health.

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2026-06-12 11:47 1mo ago
2026-04-15 04:27 3mo ago
Roivant Sciences Ltd. (NASDAQ:ROIV) Given Consensus Rating of “Moderate Buy” by Brokerages
ROIV Roivant Sciences
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Posted by Defense World Staff on Apr 15th, 2026

Roivant Sciences Ltd. (NASDAQ:ROIV – Get Free Report) has earned a consensus recommendation of “Moderate Buy” from the eleven brokerages that are covering the stock, MarketBeat Ratings reports. One equities research analyst has rated the stock with a sell rating, one has given a hold rating and nine have given a buy rating to the company. The average 12-month price objective among brokerages that have issued ratings on the stock in the last year is $29.50.

ROIV has been the topic of a number of analyst reports. Weiss Ratings downgraded shares of Roivant Sciences from a “hold (c-)” rating to a “sell (d)” rating in a research note on Monday, February 9th. HC Wainwright lifted their target price on shares of Roivant Sciences from $33.00 to $34.00 and gave the stock a “buy” rating in a research note on Wednesday, March 4th. Citigroup lifted their target price on shares of Roivant Sciences from $26.00 to $35.00 and gave the stock a “buy” rating in a research note on Tuesday, February 10th. Jefferies Financial Group reaffirmed a “buy” rating on shares of Roivant Sciences in a research note on Tuesday, March 3rd. Finally, Sanford C. Bernstein began coverage on shares of Roivant Sciences in a research note on Friday, March 20th. They issued an “outperform” rating and a $35.00 price target on the stock.

View Our Latest Report on ROIV

Insiders Place Their Bets In other news, CAO Jennifer Humes sold 13,538 shares of the business’s stock in a transaction that occurred on Wednesday, April 8th. The shares were sold at an average price of $28.37, for a total value of $384,073.06. Following the sale, the chief accounting officer directly owned 84,191 shares of the company’s stock, valued at approximately $2,388,498.67. The trade was a 13.85% decrease in their position. The transaction was disclosed in a legal filing with the Securities & Exchange Commission, which is available at this hyperlink. Also, Director Melissa B. Epperly sold 41,861 shares of the business’s stock in a transaction that occurred on Monday, March 16th. The shares were sold at an average price of $28.68, for a total transaction of $1,200,573.48. Following the completion of the sale, the director directly owned 15,804 shares in the company, valued at $453,258.72. This trade represents a 72.59% decrease in their ownership of the stock. The SEC filing for this sale provides additional information. In the last ninety days, insiders sold 4,595,624 shares of company stock worth $124,848,136. Insiders own 10.80% of the company’s stock.

Institutional Investors Weigh In On Roivant Sciences A number of institutional investors and hedge funds have recently made changes to their positions in the stock. Creek Drive Management Group LLC purchased a new stake in shares of Roivant Sciences in the 4th quarter valued at approximately $3,689,000. Hsbc Holdings PLC purchased a new stake in shares of Roivant Sciences in the 4th quarter valued at approximately $896,000. Pacer Advisors Inc. raised its stake in shares of Roivant Sciences by 24.0% in the 4th quarter. Pacer Advisors Inc. now owns 70,259 shares of the company’s stock valued at $1,525,000 after acquiring an additional 13,609 shares during the period. Dorsey Wright & Associates purchased a new stake in shares of Roivant Sciences in the 4th quarter valued at approximately $8,162,000. Finally, Invesco Ltd. raised its stake in shares of Roivant Sciences by 28.9% in the 4th quarter. Invesco Ltd. now owns 2,281,487 shares of the company’s stock valued at $49,508,000 after acquiring an additional 512,129 shares during the period. 64.76% of the stock is owned by hedge funds and other institutional investors.

Roivant Sciences Price Performance Shares of ROIV stock opened at $29.12 on Wednesday. The firm’s 50-day moving average is $27.68 and its two-hundred day moving average is $22.94. Roivant Sciences has a 12 month low of $9.90 and a 12 month high of $30.33. The company has a market capitalization of $20.84 billion, a PE ratio of -24.89 and a beta of 1.20.

About Roivant Sciences (Get Free Report)

Roivant Sciences is a biopharmaceutical company focused on the development and commercialization of innovative therapies through a network of subsidiary businesses known as “Vants.” Founded in 2014, Roivant acquires or in-licenses clinical-stage assets that have progressed beyond proof of concept and seeks to advance them efficiently toward regulatory approval. By organizing each program into a dedicated subsidiary, the company aims to streamline decision-making, allocate resources more effectively, and accelerate development timelines.

The core activities of Roivant involve identifying promising drug candidates across a range of therapeutic areas, including neurology, rare diseases, immunology, oncology, and women’s health.

Further Reading Five stocks we like better than Roivant Sciences

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2026-06-12 11:47 1mo ago
2026-04-29 11:05 2mo ago
Roivant Sciences: Moderna Settlement And Brepocitinib Support A Long-Term Buy
ROIV Roivant Sciences
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I believe my original bull case on Roivant Sciences has largely played out, with the stock up sharply since my initial coverage. Brepocitinib is clearly now becoming a broader immunology franchise across DM, NIU, CS, and LPP. ROIV also settled with Moderna regarding LNP, which adds to its already cash-rich balance sheet and supports its ongoing buybacks and pipeline.
2026-06-12 11:47 1mo ago
2026-05-11 16:05 2mo ago
Immunovant to Report Financial Results for the Fourth Quarter and Fiscal Year Ended March 31, 2026, and Provide Business Update on Wednesday, May 20, 2026
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DURHAM, N.C., May 11, 2026 (GLOBE NEWSWIRE) -- Immunovant (Nasdaq: IMVT) today announced that it will report its financial results for the fourth quarter and fiscal year ended March 31, 2026, and provide a business update at 8:00 a.m.
2026-06-12 11:47 1mo ago
2026-05-11 16:05 2mo ago
Roivant to Report Financial Results for the Fourth Quarter and Fiscal Year Ended March 31, 2026 and Provide Business Update on Wednesday, May 20, 2026
ROIV Roivant Sciences
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BASEL, Switzerland and LONDON and NEW YORK, May 11, 2026 (GLOBE NEWSWIRE) -- Roivant (Nasdaq: ROIV) today announced that it will host a live conference call and webcast at 8:00 a.m. ET on Wednesday, May 20, 2026, to report its financial results for the fourth quarter and fiscal year ended March 31, 2026, and provide a business update.
2026-06-12 11:47 1mo ago
2026-05-13 16:50 2mo ago
Roivant Sciences Ltd. (ROIV) Presents at Bank of America Global Healthcare Conference 2026 Transcript
ROIV Roivant Sciences
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Roivant Sciences Ltd. (ROIV) Presents at Bank of America Global Healthcare Conference 2026 Transcript
2026-06-12 11:47 1mo ago
2026-05-19 13:01 2mo ago
Montes Archimedes Acquisition (ROIV) Upgraded to Buy: Here's Why
ROIV Roivant Sciences
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Roivant Sciences Ltd. (ROIV - Free Report) appears an attractive pick, as it has been recently upgraded to a Zacks Rank #2 (Buy). This upgrade is essentially a reflection of an upward trend in earnings estimates -- one of the most powerful forces impacting stock prices.

The sole determinant of the Zacks rating is a company's changing earnings picture. The Zacks Consensus Estimate -- the consensus of EPS estimates from the sell-side analysts covering the stock -- for the current and following years is tracked by the system.

Individual investors often find it hard to make decisions based on rating upgrades by Wall Street analysts, since these are mostly driven by subjective factors that are hard to see and measure in real time. In these situations, the Zacks rating system comes in handy because of the power of a changing earnings picture in determining near-term stock price movements.

Therefore, the Zacks rating upgrade for Montes Archimedes Acquisition basically reflects positivity about its earnings outlook that could translate into buying pressure and an increase in its stock price.

Most Powerful Force Impacting Stock PricesThe change in a company's future earnings potential, as reflected in earnings estimate revisions, and the near-term price movement of its stock are proven to be strongly correlated. That's partly because of the influence of institutional investors that use earnings and earnings estimates for calculating the fair value of a company's shares. An increase or decrease in earnings estimates in their valuation models simply results in higher or lower fair value for a stock, and institutional investors typically buy or sell it. Their transaction of large amounts of shares then leads to price movement for the stock.

For Montes Archimedes Acquisition, rising earnings estimates and the consequent rating upgrade fundamentally mean an improvement in the company's underlying business. And investors' appreciation of this improving business trend should push the stock higher.

Harnessing the Power of Earnings Estimate RevisionsAs empirical research shows a strong correlation between trends in earnings estimate revisions and near-term stock movements, tracking such revisions for making an investment decision could be truly rewarding. Here is where the tried-and-tested Zacks Rank stock-rating system plays an important role, as it effectively harnesses the power of earnings estimate revisions.

The Zacks Rank stock-rating system, which uses four factors related to earnings estimates to classify stocks into five groups, ranging from Zacks Rank #1 (Strong Buy) to Zacks Rank #5 (Strong Sell), has an impressive externally-audited track record, with Zacks Rank #1 stocks generating an average annual return of +25% since 1988. You can see the complete list of today's Zacks #1 Rank (Strong Buy) stocks here >>>> .

Earnings Estimate Revisions for Montes Archimedes AcquisitionFor the fiscal year ending March 2026, this company is expected to earn -$1.07 per share, which is unchanged compared with the year-ago reported number.

Analysts have been steadily raising their estimates for Montes Archimedes Acquisition. Over the past three months, the Zacks Consensus Estimate for the company has increased 27.4%.

Bottom LineUnlike the overly optimistic Wall Street analysts whose rating systems tend to be weighted toward favorable recommendations, the Zacks rating system maintains an equal proportion of "buy" and "sell" ratings for its entire universe of more than 4,000 stocks at any point in time. Irrespective of market conditions, only the top 5% of the Zacks-covered stocks get a "Strong Buy" rating and the next 15% get a "Buy" rating. So, the placement of a stock in the top 20% of the Zacks-covered stocks indicates its superior earnings estimate revision feature, making it a solid candidate for producing market-beating returns in the near term.

You can learn more about the Zacks Rank here >>>

The upgrade of Montes Archimedes Acquisition to a Zacks Rank #2 positions it in the top 20% of the Zacks-covered stocks in terms of estimate revisions, implying that the stock might move higher in the near term.
2026-06-12 11:47 1mo ago
2026-05-20 07:00 2mo ago
Roivant Reports Financial Results for the Fourth Quarter and Fiscal Year Ended March 31, 2026 and Provides Business Update
ROIV Roivant Sciences
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BASEL, Switzerland and LONDON and NEW YORK, May 20, 2026 (GLOBE NEWSWIRE) -- Roivant (Nasdaq: ROIV) today reported its financial results for the fourth quarter and fiscal year ended March 31, 2026, and provided a business update.
2026-06-12 11:47 1mo ago
2026-05-20 09:15 2mo ago
Roivant Sciences Ltd. (ROIV) Reports Q4 Loss, Misses Revenue Estimates
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Roivant Sciences Ltd. (ROIV - Free Report) came out with a quarterly loss of $0.36 per share versus the Zacks Consensus Estimate of a loss of $0.26. This compares to a loss of $0.22 per share a year ago. These figures are adjusted for non-recurring items.

This quarterly report represents an earnings surprise of -41.18%. A quarter ago, it was expected that this company would post a loss of $0.27 per share when it actually produced a loss of $0.24, delivering a surprise of +11.11%.

Over the last four quarters, the company has surpassed consensus EPS estimates two times.

Montes Archimedes Acquisition, which belongs to the Zacks Medical - Biomedical and Genetics industry, posted revenues of $2.52 million for the quarter ended March 2026, missing the Zacks Consensus Estimate by 8.56%. This compares to year-ago revenues of $7.57 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.

Montes Archimedes Acquisition shares have added about 30% since the beginning of the year versus the S&P 500's gain of 7.4%.

What's Next for Montes Archimedes Acquisition?While Montes Archimedes Acquisition has outperformed 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 Montes Archimedes Acquisition was favorable. 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 #2 (Buy) for the stock. So, the shares are expected to outperform 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 -$0.24 on $2 million in revenues for the coming quarter and -$0.58 on $131.57 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 - Biomedical and Genetics is currently in the bottom 45% 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.

VistaGen Therapeutics, Inc. (VTGN - Free Report) , another stock in the same industry, has yet to report results for the quarter ended March 2026.

This company is expected to post quarterly loss of $0.42 per share in its upcoming report, which represents a year-over-year change of +2.3%. The consensus EPS estimate for the quarter has remained unchanged over the last 30 days.

VistaGen Therapeutics, Inc.'s revenues are expected to be $0.5 million, up 5100% from the year-ago quarter.
2026-06-12 11:47 1mo ago
2026-05-20 10:08 2mo ago
Roivant Sciences Q4 Earnings Call Highlights
ROIV Roivant Sciences
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Trump Index: 6 Companies Linked to Trump’s Cabinet Worth WatchingRoivant Sciences NASDAQ: ROIV executives used the company’s fourth-quarter earnings call to highlight new open-label data for IMVT-1402 in difficult-to-treat rheumatoid arthritis, upcoming pulmonary hypertension data for mosliciguat and continued preparation for a potential brepocitinib launch in dermatomyositis.

Chief Executive Matt Gline called the company’s recent period “a pretty wild 12 months,” citing progress across development programs and the previously announced $2.25 billion settlement with Moderna. Gline said Roivant expects to receive the first $950 million upfront portion of that settlement in July.

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IMVT-1402 Shows Open-Label Activity in Refractory RA The most prominent update centered on preliminary data from the open-label portion of the 1402 study in difficult-to-treat rheumatoid arthritis, or D2T RA. Gline described the results as “surprisingly good,” while cautioning that the data came from an open-label phase of the trial.

The study enrolled heavily refractory patients who had failed steroids and DMARDs as well as at least two advanced lines of therapy. Gline said 65% of patients had failed JAK inhibitors, and that “basically every single one” of those patients had also failed a TNF inhibitor. The study also required autoantibody positivity using ACPA criteria.

In the preliminary period 1 data, Roivant reported that roughly 73% of evaluable patients achieved an ACR20 response. More than half achieved ACR50, and more than one-third achieved ACR70. Gline said the depth of response was especially notable because placebo responses are less common at the ACR50 and ACR70 levels.

“It feels to us like looking at this data, there’s something going on that’s meaningful and interesting with this drug,” Gline said.

Gline said the responses were “basically fully preserved” in the subset of patients who had prior JAK inhibitor exposure, a group he characterized as both JAK- and TNF-experienced. He said the findings support the biological thesis that ACPA positivity may represent a mechanism distinct from other anti-inflammatory approaches.

The randomized withdrawal portion of the study is still ongoing. Gline said more than half of patients remain on study treatment, and the company does not yet have data from period 2. He also noted that period 2 may be harder to interpret because patients with deep ACR50 or ACR70 responses may take time to lose an ACR20 response after withdrawal.

Roivant expects to share additional analysis, including patient-level data and feedback from discussions with the U.S. Food and Drug Administration, in the second half of the year. Gline said the company is preparing to discuss the data with regulators and hopes to outline next steps for the program.

Mosliciguat Data Expected in Second Half Roivant also provided a detailed preview of mosliciguat, an inhaled soluble guanylate cyclase, or sGC, activator being studied in pulmonary hypertension associated with interstitial lung disease, or PH-ILD. Drew Fromkin, CEO of Pulmovant, said mosliciguat is designed to activate sGC directly in the lungs and potentially address both pulmonary vascular disease and lung parenchymal disease.

Fromkin said Bayer previously studied mosliciguat in 170 participants, including healthy volunteers and pulmonary hypertension patients, before Roivant’s program advanced into PH-ILD. In phase I-B data, he said a single dose produced a mean pulmonary vascular resistance reduction of more than 30% and a mean peak reduction of about 38%. He also said the drug was well-tolerated, with mild to moderate treatment-emergent adverse events and no clinically meaningful systemic blood pressure or heart rate effects.

The ongoing PHocus phase II study enrolled 135 patients, above its target of 120. Fromkin said more than 95% of participants reached and sustained the 4-milligram dose through week 16. The primary endpoint is change from baseline in pulmonary vascular resistance at week 16, with secondary measures including six-minute walk distance and NT-proBNP.

Gline emphasized that the study is not powered to show a statistically significant benefit on six-minute walk distance. He said Roivant is primarily looking for confirmation of dosing, safety and pulmonary vascular resistance effects in the patient population.

Brepocitinib Launch Preparation Continues Roivant also updated investors on brepocitinib, which Gline said could potentially launch in dermatomyositis by the end of September if the FDA review proceeds as expected. He said the company is engaged in payer discussions, physician outreach, specialty pharmacy partnerships and unbranded patient engagement.

Gline said brepocitinib was awarded breakthrough therapy designation and rare therapy designation for cutaneous sarcoidosis. Roivant expects a phase III study in cutaneous sarcoidosis to begin this year. The company also recently announced lichen planopilaris, or LPP, as a fourth indication for brepocitinib, and Gline said that study is already enrolling.

For dermatomyositis, Gline described a high unmet need, noting that many patients rely on steroids, IVIG or off-label therapies. He said phase III brepocitinib data were published in the New England Journal of Medicine in March, which he called a testament to the importance and quality of the study.

Financial Position and Upcoming Milestones Gline said Roivant ended March 31 with $4.3 billion in cash and equivalents, before receipt of the Moderna settlement payment, and no debt. He also said the company continued to retire shares during the quarter.

Key milestones discussed on the call include:

Potential brepocitinib launch in dermatomyositis by the end of September, pending FDA action. Phase III top-line data in noninfectious uveitis expected in the second half of the year. Mosliciguat phase II-B top-line data in PH-ILD expected in the second half of 2026. Additional IMVT-1402 analysis in D2T RA, including FDA feedback, expected in the second half. IMVT-1402 data in Graves’ disease and myasthenia gravis expected in 2027. Gline said Roivant’s portfolio has “as much in the windshield as in the rearview mirror,” pointing to multiple data readouts and potential commercial activities ahead.

About Roivant Sciences NASDAQ: ROIVRoivant Sciences is a biopharmaceutical company focused on the development and commercialization of innovative therapies through a network of subsidiary businesses known as “Vants.” Founded in 2014, Roivant acquires or in-licenses clinical-stage assets that have progressed beyond proof of concept and seeks to advance them efficiently toward regulatory approval. By organizing each program into a dedicated subsidiary, the company aims to streamline decision-making, allocate resources more effectively, and accelerate development timelines.

The core activities of Roivant involve identifying promising drug candidates across a range of therapeutic areas, including neurology, rare diseases, immunology, oncology, and women's health.

This instant news alert was generated by narrative science technology and financial data from MarketBeat in order to provide readers with the fastest reporting and unbiased coverage. Please send any questions or comments about this story to [email protected].

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2026-06-12 11:47 1mo ago
2026-05-20 18:20 2mo ago
Roivant Sciences Ltd. (ROIV) Q4 2025 Earnings Call Transcript
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Roivant Sciences Ltd. (ROIV) Q4 2025 Earnings Call Transcript
2026-06-12 11:47 1mo ago
2026-05-21 13:09 2mo ago
Roivant: Immunovant's Rheumatoid Arthritis Win Validates The Buy
ROIV Roivant Sciences
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Roivant (ROIV) remains a Buy as its unique 'vant' structure rapidly advances and monetizes blockbuster assets, notably through Immunovant's IMVT-1402 in rheumatoid arthritis. IMVT-1402 delivered strong Phase 2 efficacy in difficult-to-treat rheumatoid arthritis, with ACR20/50/70 rates of 72.7%, 54.5%, and 35.8%, respectively. ROIV's financial position is robust, ending the quarter with $4.3 billion in cash and a management-asserted runway to profitability.
2026-06-12 11:47 1mo ago
2026-05-29 17:24 1mo ago
Roivant Sciences Ltd. (ROIV) Presents at Bernstein 42nd Annual Strategic Decisions Conference Transcript
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Roivant Sciences Ltd. (ROIV) Presents at Bernstein 42nd Annual Strategic Decisions Conference Transcript
2026-06-12 11:47 1mo ago
2026-06-03 18:32 1mo ago
Roivant Sciences Ltd. (ROIV) Presents at Jefferies Global Healthcare Conference 2026 Transcript
ROIV Roivant Sciences
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Roivant Sciences Ltd. (ROIV) Presents at Jefferies Global Healthcare Conference 2026 Transcript
2026-06-12 11:47 1mo ago
2026-06-09 20:22 1mo ago
Roivant Sciences Ltd. (ROIV) Presents at Goldman Sachs 47th Annual Global Healthcare Conference 2026 Transcript
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Roivant Sciences Ltd. (ROIV) Presents at Goldman Sachs 47th Annual Global Healthcare Conference 2026 Transcript
2026-06-12 11:47 1mo ago
2026-04-27 16:01 2mo ago
Intellia Announces Proposed Public Offering of Common Stock
NTLA Intellia Therapeutics
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April 27, 2026 16:01 ET  | Source: Intellia Therapeutics, Inc.

CAMBRIDGE, Mass., April 27, 2026 (GLOBE NEWSWIRE) -- Intellia Therapeutics, Inc. (Nasdaq: NTLA), a leading biopharmaceutical company focused on revolutionizing medicine leveraging CRISPR gene editing and other core technologies, today announced that it has commenced an underwritten public offering of $150 million of shares of its common stock. Intellia also intends to grant the underwriters a 30-day option to purchase up to an additional fifteen percent (15%) of the shares of common stock offered in the public offering. All of the shares in the proposed offering are to be sold by Intellia.

Jefferies, Goldman Sachs & Co. LLC and Citigroup are acting as joint book-running managers for the proposed offering. The offering is subject to market and other conditions, and there can be no assurance as to whether or when the offering may be completed, or as to the actual size or terms of the offering.

The shares of common stock are being offered by Intellia pursuant to an automatic shelf registration statement on Form S-3ASR (File No. 333-275740) that was previously filed with the U.S. Securities and Exchange Commission (SEC) on November 24, 2023 and automatically became effective upon filing. A preliminary prospectus supplement and accompanying prospectus relating to and describing the terms of the offering will be filed with the SEC and may be obtained, when available, from: Jefferies LLC, by mail at Attn: Equity Syndicate Prospectus Department, 520 Madison Avenue, New York, NY 10022, by telephone at (877) 821-7388, or by email at [email protected]; Goldman Sachs & Co. LLC, by mail at Attention: Prospectus Department, 200 West Street, New York, NY 10282, by telephone at (866) 471-2526, or by email at [email protected]; or Citigroup, c/o Broadridge Financial Solutions, 1155 Long Island Avenue, Edgewood, NY 11717 (Tel: 800-831-9146).

This press release shall not constitute an offer to sell or the solicitation of an offer to buy these securities, nor shall there be any sale of these securities in any state or jurisdiction in which such offer, solicitation or sale would be unlawful prior to registration or qualification under the securities laws of any such state or jurisdiction.

About Intellia Therapeutics
Intellia Therapeutics, Inc. (Nasdaq: NTLA) is a leading clinical-stage biopharmaceutical company focused on revolutionizing medicine leveraging CRISPR gene editing and other core technologies. The company’s mission is to transform the lives of people with severe diseases by developing and commercializing potentially curative treatments. With deep scientific, technical and clinical development experience, Intellia aims to reset the standard for medicine by durably treating the root causes of disease.

Forward-Looking Statements
This press release contains “forward-looking statements” of Intellia Therapeutics, Inc. (“Intellia” or the “Company”) within the meaning of the Private Securities Litigation Reform Act of 1995. These forward-looking statements include, but are not limited to, express or implied statements regarding Intellia’s beliefs and expectations regarding the proposed public offering; uncertainties related to market conditions and statements regarding the timing, size and expected proceeds of the proposed public offering; the safety, tolerability, efficacy, advancement and success of Intellia’s clinical programs; and Intellia’s ability to successfully execute its business and strategic plans, including the advancement, development and commercialization of its product candidates.

Any forward-looking statements in this press release are based on management’s current expectations and beliefs of future events and are subject to a number of risks and uncertainties that could cause actual results to differ materially and adversely from those set forth in or implied by such forward-looking statements. These risks and uncertainties include, but are not limited to: risks related to Intellia’s ability to protect and maintain its intellectual property position; risks related to valid third party intellectual property; risks related to Intellia’s relationship with third parties, including its licensors and licensees; risks related to the ability of its licensors to protect and maintain their intellectual property position; uncertainties related to regulatory agencies’ evaluation of regulatory filings and other information related to our product candidates, including nex-z; uncertainties related to the authorization, initiation and conduct of studies and other development requirements for our product candidates, including uncertainties related to regulatory approvals to conduct clinical trials; the risk that any one or more of Intellia’s product candidates will not be successfully developed and commercialized; the risk that the results of preclinical studies or clinical studies will not be predictive of future results in connection with future studies for the same product candidate or Intellia’s other product candidates; and risks related to Intellia’s reliance on collaborations, including that its collaboration with Regeneron Pharmaceuticals, Inc. will not continue or will not be successful. For a discussion of these and other risks and uncertainties, and other important factors, any of which could cause Intellia’s actual results to differ from those contained in the forward-looking statements, see the section entitled “Risk Factors” in Intellia’s most recent annual report on Form 10-K, as well as discussions of potential risks, uncertainties, and other important factors in Intellia’s other filings with the Securities and Exchange Commission, including its quarterly reports on Form 10-Q. All information in this press release is as of the date of the release, and Intellia undertakes no duty to update this information unless required by law.

Investor Contact:
Jason Fredette
Vice President, Investor Relations and Corporate Communications
Intellia Therapeutics, Inc.
[email protected]

Media Contact:
Mike Tattory
Vice President
LifeSci Communications
[email protected]
2026-06-12 11:47 1mo ago
2026-04-28 14:06 2mo ago
NTLA Falls 4% Despite Strong Phase III HAE Data, Initiates Rolling BLA
NTLA Intellia Therapeutics
FMP Stock News
Original source text
Key Takeaways Intellia shares fell 4% despite the phase III data meeting all endpoints for lonvo-z in HAE.NTLA's lonvo-z cut HAE attacks by 87% vs. placebo, with 62% of patients attack-free in the study.Intellia began its rolling BLA submission, targeting completion in H2 2026 and a launch in 2027. Shares of Intellia Therapeutics (NTLA - Free Report) declined 4% on Monday despite positive top-line data from the global phase III HAELO clinical trial evaluating lonvo-z for the treatment of patients with hereditary angioedema (HAE). Lonvo-z is a one-time, outpatient CRISPR-based therapy designed to inactivate the KLKB1 gene, thereby reducing kallikrein and bradykinin levels.

Key Highlights of NTLA’s Phase III HAELO StudyThe phase III randomized, placebo-controlled HAELO study evaluated the safety and efficacy of a one-time 50-milligram dose of lonvo-z in patients aged 16 years and older with type I or type II HAE. Data from the study demonstrated that a one-time infusion of lonvo-z reduced HAE attacks by 87% compared with placebo over the six-month evaluation period. Patients treated with lonvo-z had a much lower average monthly attack rate (0.26) versus 2.10 in the placebo group.

The study met its primary endpoint. It also met all key secondary endpoints with strong statistical significance, including a notably higher proportion of patients who were completely free from both attacks and ongoing therapy (62% versus 11% with placebo). The treatment was well-tolerated, with mild-to-moderate side effects.

Hereditary angioedema (HAE) is a rare genetic disorder marked by recurrent, potentially life-threatening swelling caused by excess bradykinin.

However, it seems that investors were not impressed by the data reported by the company and its stock declined.

Year to date, shares of NTLA have risen 45% against the industry’s 1.2% decline.

Image Source: Zacks Investment Research

NTLA Initiates Rolling Submission of BLA for lonvo-zIn a separate press release, Intellia announced that it has begun a rolling submission of a biologics license application (BLA) to the FDA seeking approval for lonvo-z for the treatment of HAE.

The company expects to complete the BLA submission in the second half of 2026. If accepted, the FDA will determine whether the application qualifies for priority review and will set a target decision date. Intellia plans to commercially launch lonvo-z in the first half of 2027, as the world’s first in vivo CRISPR-based gene editing therapy, if approved.

NTLA’s Zacks Rank & Stocks to ConsiderIntellia Therapeutics currently carries a Zacks Rank #3 (Hold).

Some better-ranked stocks in the biotech sector are Catalyst Pharmaceuticals (CPRX - Free Report) , currently sporting a Zacks Rank #1 (Strong Buy), and Indivior Pharmaceuticals (INDV - Free Report) and ANI Pharmaceuticals (ANIP - Free Report) , which carry a Zacks Rank #2 (Buy). You can see the complete list of today’s Zacks #1 Rank stocks here.

Over the past 60 days, estimates for Catalyst Pharmaceuticals’ 2026 earnings per share have risen from $2.59 to $2.87. Over the same period, EPS estimates for 2027 have surged from $3.01 to $3.25. CPRX shares have gained 25.5% year to date.

Catalyst Pharmaceuticals’ earnings beat estimates in each of the trailing four quarters, with the average surprise being 35.19%.

Over the past 90 days, estimates for Indivior Pharmaceuticals’ 2026 earnings per share have risen from $2.94 to $3.00. Over the same period, EPS estimates for 2027 have surged from $3.22 to $3.29. INDV shares have lost 4.4% year to date.

Indivior Pharmaceuticals’ earnings beat estimates in each of the trailing four quarters, with the average surprise being 74.53%.

Over the past 60 days, estimates for ANI Pharmaceuticals’ 2026 earnings per share have increased from $8.22 to $9.02. Over the same period, EPS estimates for 2027 have risen from $9.90 to $10.23. Year to date, shares of ANIP have gained 0.8%.

ANI Pharmaceuticals' earnings beat estimates in each of the trailing four quarters, with the average surprise being 22.21%.
2026-06-12 11:47 1mo ago
2026-04-29 06:27 2mo ago
Cathie Wood just made a massive bet on these two top AI stocks
NTLA Intellia Therapeutics
FMP Stock News
Original source text
While the heyday of Cathie Wood’s investment management is, for the time being, firmly in the past, the popular ARK Innovation ETF (ARKK) has been having a respectable run in the last 12 months and unveiled its latest series of bets as recently as April 28.

ARKK ETF one-year price chart. Source: Google Specifically, ARKK revealed on Tuesday that it invested a total of nearly $42 million in four stocks: Alphabet (NASDAQ: GOOG), CoreWeave (NASDAQ: CRWV), Intellia Therapeutics (NASDAQ: NTLA), and Kratos Defense & Security Solutions (NASDAQ: KTOS).

The purchases of NTLA and KTOS shares ranged between $6 and $6.9 million, and together, the two account for just 0.13% of the exchange-traded fund (ETF).

Simultaneously, the market value of the April 28 Google stock investment is listed at $14.1 million – 0.14% of the ETF – and in CoreWeave at $14.8 million – 0.15%.

ARKK ETF April 28 investments. Source: Cathie’s Ark Cathie Wood invests $14.8 million in CoreWeave stock Elsewhere, the timing of the two bigger investments is interesting for a variety of reasons. CoreWeave is, as a company, seen as either a firm that is doomed to collapse or one of the most exciting investment opportunities of 2026.

Indeed, the former cryptocurrency miner made a pivot to becoming an artificial intelligence (AI) data center, securing backing from the semiconductor giant Nvidia (NASDAQ: NVDA). 

Under the circumstances, Cathie Wood appears to be betting that the optimistic predictions regarding the advancements, proliferation, and adoption of AI made by many executives and Wall Street experts will prove correct, enabling CoreWeave to enjoy a veritable explosion of revenue and profits.

The risk associated with the investment, however, comes from a mix of factors, of which the fact that AI model usage remains subsidized, limiting eventual full adoption, and the many data center delays and cancellations are the most pointed.

Lastly, the buy appears to have been timed with the latest CRWV correction, considering the equity rallied 77% between March 30 and April 22, but then fell 13.88% to $105.53 on April 28.

Cathie Wood invests $14.1 million in Google stock Google, on the other hand, is a trade that came without a correction in the latest rally but appears to simultaneously be a bet that the blue-chip technology giant will offer impressive earnings after the closing bell on April 29, thus bolstering the upward momentum.

Google stock price YTD chart. Source: Finbold Looking long-term, Alphabet has been a relatively safe bet for decades due to its dominant market position, continued search engine leadership, and the foresight that enabled it to participate in multiple technology trends, including becoming one of the top companies in the ongoing AI boom.

Still, Google is somewhat exposed in the long term since it has made a significant bet that the current AI race will continue without major setbacks, while, according to numerous users, severely degrading the quality of its core search engine business over the last decade.

Featured image via Shutterstock
2026-06-12 11:47 1mo ago
2026-04-29 07:00 2mo ago
Intellia Therapeutics Announces Pricing of Public Offering of Common Stock
NTLA Intellia Therapeutics
FMP Stock News
Original source text
April 29, 2026 07:00 ET  | Source: Intellia Therapeutics, Inc.

CAMBRIDGE, Mass., April 29, 2026 (GLOBE NEWSWIRE) -- Intellia Therapeutics, Inc. (Nasdaq: NTLA), a leading biopharmaceutical company focused on revolutionizing medicine leveraging CRISPR gene editing and other core technologies, today announced the pricing of an underwritten public offering of 16,744,187 shares of its common stock. The shares of common stock are being sold at a public offering price of $10.75 per share. The gross proceeds from the offering, before deducting underwriting discounts and commissions and offering expenses, are expected to be approximately $180 million, excluding any exercise of the underwriters' option to purchase additional shares. All of the securities in the offering are to be sold by Intellia. In addition, Intellia has granted the underwriters a 30-day option to purchase up to 2,511,628 additional shares of its common stock at the public offering price, less the underwriting discounts and commissions.

Jefferies, Goldman Sachs & Co. LLC and Citigroup are acting as joint book-running managers for the offering. The offering is subject to market and other conditions, and there can be no assurance as to whether or when the offering may be completed, or as to the actual size or terms of the offering.

The shares of common stock are being offered by Intellia pursuant to an automatic shelf registration statement on Form S-3ASR (File No. 333-275740) that was previously filed with the U.S. Securities and Exchange Commission (SEC) on November 24, 2023 and automatically became effective upon filing. A preliminary prospectus supplement relating to and describing the terms of the offering was filed with the SEC on April 27, 2026. The final prospectus supplement and accompanying prospectus relating to and describing the terms of the offering will be filed with the SEC and may be obtained, when available, from: Jefferies LLC by mail at Attn: Equity Syndicate Prospectus Department, 520 Madison Avenue, New York, NY 10022, by telephone at (877) 821-7388, or by email at [email protected]; Goldman Sachs & Co. LLC, Attention: Prospectus Department, 200 West Street, New York, NY 10282, by telephone at (866) 471-2526, or by email at [email protected]; or Citigroup, c/o Broadridge Financial Solutions, 1155 Long Island Avenue, Edgewood, NY 11717 (Tel: 800-831-9146).

This press release shall not constitute an offer to sell or the solicitation of an offer to buy these securities, nor shall there be any sale of these securities in any state or jurisdiction in which such offer, solicitation or sale would be unlawful prior to registration or qualification under the securities laws of any such state or jurisdiction.

About Intellia Therapeutics
Intellia Therapeutics, Inc. (Nasdaq: NTLA) is a leading clinical-stage biopharmaceutical company focused on revolutionizing medicine leveraging CRISPR gene editing and other core technologies. The company’s mission is to transform the lives of people with severe diseases by developing and commercializing potentially curative treatments. With deep scientific, technical and clinical development experience, Intellia aims to reset the standard for medicine by durably treating the root causes of disease.

Forward-Looking Statements
This press release contains “forward-looking statements” of Intellia Therapeutics, Inc. (“Intellia” or the “Company”) within the meaning of the Private Securities Litigation Reform Act of 1995. These forward-looking statements include, but are not limited to, express or implied statements regarding Intellia’s beliefs and expectations regarding Intellia’s anticipated public offering; uncertainties related to market conditions and statements regarding the timing, size and expected proceeds of the anticipated offering; the safety, tolerability, efficacy, advancement and success of Intellia’s clinical programs; and Intellia’s ability to successfully execute its business and strategic plans, including the advancement, development and commercialization of its product candidates.

Any forward-looking statements in this press release are based on management’s current expectations and beliefs of future events and are subject to a number of risks and uncertainties that could cause actual results to differ materially and adversely from those set forth in or implied by such forward-looking statements. These risks and uncertainties include, but are not limited to: risks related to Intellia’s ability to protect and maintain its intellectual property position; risks related to valid third party intellectual property; risks related to Intellia’s relationship with third parties, including its licensors and licensees; risks related to the ability of its licensors to protect and maintain their intellectual property position; uncertainties related to regulatory agencies’ evaluation of regulatory filings and other information related to our product candidates, including nex-z; uncertainties related to the authorization, initiation and conduct of studies and other development requirements for our product candidates, including uncertainties related to regulatory approvals to conduct clinical trials; the risk that any one or more of Intellia’s product candidates will not be successfully developed and commercialized; the risk that the results of preclinical studies or clinical studies will not be predictive of future results in connection with future studies for the same product candidate or Intellia’s other product candidates; and risks related to Intellia’s reliance on collaborations, including that its collaboration with Regeneron Pharmaceuticals, Inc. will not continue or will not be successful. For a discussion of these and other risks and uncertainties, and other important factors, any of which could cause Intellia’s actual results to differ from those contained in the forward-looking statements, see the section entitled “Risk Factors” in Intellia’s most recent annual report on Form 10-K, as well as discussions of potential risks, uncertainties, and other important factors in Intellia’s other filings with the Securities and Exchange Commission, including its quarterly reports on Form 10-Q. All information in this press release is as of the date of the release, and Intellia undertakes no duty to update this information unless required by law.

Investor Contact:
Jason Fredette
Vice President, Investor Relations and Corporate Communications
Intellia Therapeutics, Inc.
[email protected]

Media Contact:
Mike Tattory
Vice President
LifeSci Communications
[email protected]
2026-06-12 11:47 1mo ago
2026-04-29 15:13 2mo ago
Intellia Therapeutics Posts Phase 3 HAELO Win for lonvo-z, Begins Rolling FDA BLA Filing
NTLA Intellia Therapeutics
FMP Stock News
Original source text
Intellia Therapeutics (NASDAQ:NTLA) highlighted top-line results from its Phase III HAELO trial evaluating lonvo-z, an investigational in vivo CRISPR-based gene-editing therapy for hereditary angioedema (HAE), and provided an update on regulatory progress during a company conference call.

Company outlines lonvo-z strategy and HAE unmet need Chief Executive Officer John Leonard described the update as a milestone for “the entire CRISPR field” and people living with HAE, emphasizing Intellia’s focus on in vivo gene editing delivered to the liver. Leonard said Intellia was “the first in the world to dose patients with in vivo CRISPR-based candidates and the first to advance into phase III,” and characterized the newly reported results as the “world’s first phase III data for an in vivo gene-editing candidate.”

Chief Medical Officer David Lebwohl said HAE is driven by an imbalance in the kallikrein-kinin system that leads to unpredictable swelling attacks, including potentially fatal laryngeal events. Despite widespread use of long-term prophylaxis (LTP), Lebwohl said many patients still experience breakthrough attacks and face burdens from chronic treatment, including frequent administration and payer scrutiny. He estimated there are about 7,000 treated HAE patients in the U.S., with more than 60% on LTP, and said U.S. spending is “about $4 billion annually on chronic HAE medications alone,” excluding other healthcare costs.

Lebwohl said lonvo-z is designed to permanently inactivate the KLKB1 gene to reduce kallikrein and bradykinin and “reset the system.” He also described the intended administration as outpatient: patients took a steroid at home the day before dosing, then received additional premedication and a 2- to 4-hour IV infusion before going home.

Phase III HAELO design and enrollment Marc Riedl, Professor of Medicine and Clinical Director of the US HAEA Angioedema Center at UC San Diego Health and a HAELO principal investigator, presented the Phase III results. Riedl said HAELO is a placebo-controlled, double-blind, randomized trial in Type 1 and Type 2 HAE, requiring LTP washout during screening to establish an LTP-free baseline attack rate during run-in. Patients were randomized 2:1 to a one-time 50 mg dose of lonvo-z or placebo.

Riedl said the six-month efficacy evaluation period ran from week 5 through week 28 post-dosing. After week 28, patients could enter a blinded crossover and were followed for 18 additional months before long-term follow-up.

A total of 80 patients enrolled, with 52 assigned to lonvo-z and 28 to placebo. Roughly 70% of patients in each arm were female, about half were enrolled in the U.S., and approximately 70% were using LTP at study entry, with lanadelumab most common. The mean monthly attack rate during run-in was 3.5 in both arms.

Efficacy: primary endpoint and attack-free outcomes Riedl said HAELO met the primary endpoint and all key secondary endpoints with statistical significance. For the primary endpoint (weeks 5–28), the placebo arm had a mean of 2.1 attacks per month versus 0.26 for lonvo-z, an 87% reduction.

Riedl also reported that 62% of lonvo-z patients were attack-free during the efficacy observation period versus 11% on placebo. He emphasized that these patients were also “therapy-free,” taking no other prophylactic or rescue medication during that period.

Within the lonvo-z arm, Riedl said 100% of patients achieved an attack-rate reduction from baseline. He reported 62% were attack-free and therapy-free, while the remaining 38% had not reached attack-free status over the full observation period but showed a 72% reduction versus baseline. Leonard later noted that this 38% bucket could include patients who experienced a single attack early in the observation window and none thereafter, and he said Intellia plans to present more detail at the European Academy of Allergy and Clinical Immunology (EAACI) meeting in June, including swimmer plots and additional subgroup information.

Riedl said early post-crossover data suggested continued improvement, with mean monthly attack rates “near zero” by week 36 among patients who had reached that time point, though he cautioned patient numbers beyond week 28 were limited at the cutoff.

Safety, labeling considerations, and path to filing and launch Riedl said lonvo-z had a favorable safety and tolerability profile in HAELO as of the data cutoff, with all adverse events mild or moderate and no serious adverse events in the lonvo-z arm. The most common adverse events were infusion-related reactions that were mild to moderate and transient.

Leonard also addressed a question about liver tests, saying there was a single Grade 2 ALT elevation in the trial that occurred “a couple weeks out after dosing,” resolved spontaneously within a week, and was asymptomatic with no therapy provided.

On real-world expectations, Riedl said the 62% attack-free endpoint is challenging because trials rely heavily on patient-reported outcomes, which can capture variable symptoms such as abdominal pain that may be adjudicated as an HAE attack. He added that other HAE therapies often “outperformed in the real world” versus blinded trials, including in open-label extensions, as patient confidence in treatment grows over time.

Riedl said if approved, he would discuss lonvo-z with every patient, but emphasized patient preferences vary. He added that while some patients are satisfied with current therapies, “certainly half and probably more than half” of his patients still discuss ongoing attacks, symptoms, treatment burden, and interruptions due to coverage issues. He also said most patient questions about gene editing relate to long-term safety and that broader education will be important.

Riedl pushed back on the suggestion that on-demand therapies might be unnecessary, saying guidelines still recommend all patients maintain access to on-demand treatment given the risk of rare but life-threatening airway attacks, though he expects usage could decline over time.

Leonard said Intellia recently initiated a rolling biologics license application (BLA) with the FDA and is preparing for potential approval and launch, including building commercial leadership, engaging payers and advocacy groups, and identifying target treatment centers. He said the company plans to present additional data at EAACI and aims, “if approved,” to target a commercial launch in the first half of 2027.

Chief Financial Officer Edward Dulac said Intellia is considering collaboration and distribution agreements to reach patients outside the U.S. and has not disclosed timelines for non-U.S. filings. Dulac also said payer discussions have been ongoing and “very constructive,” noting payers often evaluate one-time therapies as a multiple of the average annual cost. He said the company expects lonvo-z to be priced at a premium, though no price has been set, and added that Intellia is mindful that aggressive pricing could increase resistance, including through step edits.

About Intellia Therapeutics (NASDAQ:NTLA) Intellia Therapeutics, Inc (NASDAQ: NTLA) is a clinical‐stage biotechnology company focused on developing potentially curative genome editing therapies using the CRISPR/Cas9 platform. The company’s research spans both in vivo and ex vivo applications of CRISPR/Cas9, aiming to correct or disable disease‐causing genes with a single administration. Intellia’s lead in vivo program targets transthyretin amyloidosis (ATTR) by delivering CRISPR/Cas9 machinery directly to the liver, while additional preclinical efforts pursue treatments for hemophilia A, hereditary angioedema and other genetic disorders.

Beyond its in vivo pipeline, Intellia collaborates with strategic partners to extend the impact of its genome editing approach.

Featured Articles Five stocks we like better than Intellia Therapeutics
2026-06-12 11:47 1mo ago
2026-05-01 16:01 2mo ago
Intellia Therapeutics Reports Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)
NTLA Intellia Therapeutics
FMP Stock News
Original source text
May 01, 2026 16:01 ET  | Source: Intellia Therapeutics, Inc.

CAMBRIDGE, Mass., May 01, 2026 (GLOBE NEWSWIRE) -- Intellia Therapeutics, Inc. (Nasdaq: NTLA), a leading biopharmaceutical company focused on revolutionizing medicine leveraging CRISPR gene editing and other core technologies, today announced that on May 1, 2026, it awarded inducement grants to 43 new employees under Intellia’s 2024 Inducement Plan, as amended, as a material inducement to employment.

The inducement grants consisted of time-based restricted stock units (“RSUs”) for an aggregate of 208,850 shares of Intellia’s common stock, with one-third of such RSUs vesting annually over three years. All equity vesting is subject to each employee’s continued service as an employee of, or other service provider to, Intellia through the applicable vesting dates.

All of the above-described awards were granted outside of Intellia’s stockholder-approved equity incentive plans pursuant to Intellia’s 2024 Inducement Plan, as amended, which was initially adopted by the board of directors in June 2024. These awards were approved by Intellia’s compensation committee as a material inducement to entering into employment with Intellia in accordance with Nasdaq Listing Rule 5635(c)(4).

About Intellia Therapeutics
Intellia Therapeutics, Inc. (Nasdaq: NTLA) is a leading clinical-stage biopharmaceutical company focused on revolutionizing medicine leveraging CRISPR gene editing and other core technologies. The company’s mission is to transform the lives of people with severe diseases by developing and commercializing potentially curative treatments. With deep scientific, technical and clinical development experience, Intellia aims to reset the standard for medicine by durably treating the root causes of disease. Learn more at intelliatx.com and follow us @intelliatx.

Investor Contact:
Jason Fredette
Vice President, Investor Relations and Corporate Communications
Intellia Therapeutics, Inc.
[email protected]

Media Contact:
Mike Tattory
Vice President
LifeSci Communications
[email protected]
2026-06-12 11:47 1mo ago
2026-05-05 07:30 2mo ago
Intellia Therapeutics to Participate in Upcoming Investor Conferences
NTLA Intellia Therapeutics
FMP Stock News
Original source text
May 05, 2026 07:30 ET  | Source: Intellia Therapeutics, Inc.

CAMBRIDGE, Mass., May 05, 2026 (GLOBE NEWSWIRE) -- Intellia Therapeutics, Inc. (Nasdaq: NTLA), a leading biopharmaceutical company focused on revolutionizing medicine leveraging CRISPR gene editing and other core technologies, today announced that management will be participating in fireside chats at the following upcoming investor conferences:

Bank of America Securities Health Care Conference
Date: Tuesday, May 12, 2026
Fireside Chat Time: 3:40 p.m. PT
Location: Las Vegas RBC Capital Markets Global Healthcare Conference
Date: Wednesday, May 20, 2026
Fireside Chat Time: 2:35 p.m. ET
Location: New York Jefferies Global Healthcare Conference
Date: Wednesday, June 3, 2026
Fireside Chat Time: 4:55 p.m. ET
Location: New York The fireside chats will be webcast live. To join the webcasts, please visit the Events and Presentations page of the Investors & Media section on Intellia’s website at intelliatx.com. Replays of the webcasts will be available on the same page for approximately 90 days following the events.

About Intellia Therapeutics
Intellia Therapeutics, Inc. (Nasdaq: NTLA) is a leading clinical-stage biopharmaceutical company focused on revolutionizing medicine leveraging CRISPR gene editing and other core technologies. The company’s mission is to transform the lives of people with severe diseases by developing and commercializing potentially curative treatments. With deep scientific, technical and clinical development experience, Intellia aims to reset the standard for medicine by durably treating the root causes of disease. Learn more at intelliatx.com and follow us @intelliatx.

Investor Contact:
Jason Fredette
Vice President, Investor Relations and Corporate Communications
Intellia Therapeutics, Inc.
[email protected]

Media Contact:
Mike Tattory
Vice President
LifeSci Communications
[email protected] 
2026-06-12 11:47 1mo ago
2026-05-06 10:12 2mo ago
Cathie Wood Goes Bargain Hunting: 3 Stocks She Just Bought
NTLA Intellia Therapeutics
FMP Stock News
Original source text
Tuesday was a rough day for Shopify (SHOP +2.06%), Intellia Therapeutics (NTLA +1.23%), and GeneDX Holdings (WGS +12.28%) investors. All three growth stocks tumbled between 4% and 49%. As the market was selling off those once high-flying stocks, Cathie Wood was buying.

Wood's Ark Invest added to all three existing positions on Tuesday. They were the only three stocks Ark Invest bought during the trading day. Let's take a closer look at what could be drawing the founder and CEO of Ark Invest to buy into Shopify, Intellia Therapuetics, and GeneDX on the way down.

Image source: Getty Images.

1. Shopify Let's start with the good news. Shopify stock is nearly a 50-bagger since its IPO. It's even trading higher over the past year. However, the online marketplace operator is falling again after a poorly received financial update in which soft guidance ruined an otherwise solid performance.

Revenue rose 34% for the first quarter, fueled by a 35% jump in gross merchandise volume for the merchants leaning on Shopify's e-commerce solutions. Adjusted net income fared even better, surging 44%. Both ends of the income statement exceeded expectations, but a recurring theme this earnings season has been strong quarters tripped up by a cautionary near-term tone.

Today's Change

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Now for the bad news. Shopify expects year-over-year revenue growth to decelerate in the current quarter. It's targeting an increase in the high twenties on a percentage basis. This is pretty much where Wall Street pros were anyway, but it dulls the excitement over the first quarter's 34% top-line jump.

It also doesn't help that Shopify isn't exactly cheap. Even after Tuesday's 16% slide, the stock is still trading for more than 50 times forward earnings. Thankfully, a high P/E ratio hasn't stopped Shopify before. It's still generating gobs of free cash flow, and its guidance for the new quarter should extend its streak of a double-digit free cash flow margin to 12 consecutive quarters.

This high-beta stock will remain volatile. Wood doesn't have a problem with that. She's buying as others are selling, and betting against Shopify hasn't been a winning trade for investors with long-term horizons.

Today's Change

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$

12.35

2. Intellia Therapeutics Unlike the double-digit percentage hits for the other two stocks on Wood's shopping list on Tuesday, Intellia was limited to a 4% retreat. One of Wood's most popular gene-editing stocks, the developer of next-gen treatments based on CRISPR therapies is connecting with analysts.

Whitney Ijem at Canaccord boosted his firm's price target from $48 to $58 last week, encouraged by recent positive data from a phase 3 clinical trial of a promising treatment. He's not even the Street-high on the shares. One analyst thinks Intellia is headed to $95, a big deal for a stock trading in the low teens.

Today's Change

(

12.28

%) $

6.67

Current Price

$

60.99

3. GeneDX Holdings One of Tuesday's biggest losers was GeneDX. Shares of the genomics company specializing in the diagnosis of rare diseases shed nearly half of their value after posting disappointing first-quarter results. A report has to be pretty bad for a stock to plunge 49% in a single trading day, so let's take a closer look.

Revenue rose 17% to $102.3 million through the first three months of this year. After seeing revenue soar 51% and then 40% in the past two years, analysts were holding out for a nearly 30% increase on the top line for the quarter. GeneDX's bread-and-butter exome and genome revenue rose a respectable 27%, but shortfalls elsewhere -- including its average reimbursement rates -- dragged overall results down. It also fell short of expectations on the bottom line.

This wasn't just a one-time fluke. GeneDX is resetting expectations. It now sees $475 million to $490 million in revenue for all of 2026, down from the $540 million to $555 million it was targeting earlier this year. After coming up short by $10 million on the top line in the first quarter, it's slashing the midpoint of its full-year outlook by $65 million. This appears to be a situation that will get worse instead of better in the near term.
2026-06-12 11:47 1mo ago
2026-05-07 11:01 2mo ago
Intellia Therapeutics, Inc. (NTLA) Expected to Beat Earnings Estimates: Can the Stock Move Higher?
NTLA Intellia Therapeutics
FMP Stock News
Original source text
Intellia Therapeutics, Inc. (NTLA - Free Report) is expected to deliver a year-over-year increase in earnings on lower 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 earnings report might help the stock move higher if these key numbers are better than expectations. 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 loss of $0.92 per share in its upcoming report, which represents a year-over-year change of +16.4%.

Revenues are expected to be $15.53 million, down 6.6% from the year-ago quarter.

Estimate Revisions TrendThe consensus EPS estimate for the quarter has been revised 5.31% higher 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 Intellia Therapeutics?For Intellia Therapeutics, the Most Accurate Estimate is higher than the Zacks Consensus Estimate, suggesting that analysts have recently become bullish on the company's earnings prospects. This has resulted in an Earnings ESP of +6.14%.

On the other hand, the stock currently carries a Zacks Rank of #3.

So, this combination indicates that Intellia Therapeutics will most likely 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 Intellia Therapeutics would post a loss of$0.99 per share when it actually produced a loss of -$0.83, delivering a surprise of +16.16%.

Over the last four quarters, the company has beaten consensus EPS estimates four 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.

Intellia Therapeutics appears 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.

Stay on top of upcoming earnings announcements with the Zacks Earnings Calendar.
2026-06-12 11:47 1mo ago
2026-05-11 07:30 2mo ago
Intellia Therapeutics Announces First Quarter 2026 Financial Results and Business Updates
NTLA Intellia Therapeutics
FMP Stock News
Original source text
Presented positive Phase 3 HAELO topline clinical data for lonvo-z in HAE; initiated rolling BLA submission; anticipate U. S. launch in first half of 2027 Recently resumed patient screening in MAGNITUDE and MAGNITUDE-2 Phase 3 clinical trials of nex-z in ATTR-CM and ATTRv-PN, respectively Including proceeds from underwritten public offering in April, existing cash resources expected to fund operations at least into 2028 CAMBRIDGE, Mass.
2026-06-12 11:47 1mo ago
2026-05-11 09:41 2mo ago
Intellia Therapeutics, Inc. (NTLA) Reports Q1 Loss, Misses Revenue Estimates
NTLA Intellia Therapeutics
FMP Stock News
Original source text
Intellia Therapeutics, Inc. (NTLA - Free Report) came out with a quarterly loss of $0.81 per share versus the Zacks Consensus Estimate of a loss of $0.92. This compares to a loss of $1.1 per share a year ago. These figures are adjusted for non-recurring items.

This quarterly report represents an earnings surprise of +11.60%. A quarter ago, it was expected that this company would post a loss of $0.99 per share when it actually produced a loss of $0.83, delivering a surprise of +16.16%.

Over the last four quarters, the company has surpassed consensus EPS estimates four times.

Intellia Therapeutics, which belongs to the Zacks Medical - Biomedical and Genetics industry, posted revenues of $15.05 million for the quarter ended March 2026, missing the Zacks Consensus Estimate by 3.12%. This compares to year-ago revenues of $16.63 million. The company has topped consensus revenue estimates two 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.

Intellia Therapeutics shares have added about 56.7% since the beginning of the year versus the S&P 500's gain of 8.1%.

What's Next for Intellia Therapeutics?While Intellia Therapeutics has outperformed 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 Intellia Therapeutics 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 -$0.86 on $15.13 million in revenues for the coming quarter and -$3.50 on $68.64 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 - Biomedical and Genetics is currently in the bottom 42% 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.

One other stock from the same industry, Gossamer Bio (GOSS - Free Report) , is yet to report results for the quarter ended March 2026.

This biopharmaceutical company is expected to post quarterly loss of $0.18 per share in its upcoming report, which represents a year-over-year change of -12.5%. The consensus EPS estimate for the quarter has remained unchanged over the last 30 days.

Gossamer Bio's revenues are expected to be $5.57 million, down 43.7% from the year-ago quarter.
2026-06-12 11:47 1mo ago
2026-05-12 12:47 2mo ago
NTLA Q1 Earnings Beat Estimates, Revenues Miss Mark, Pipeline in Focus
NTLA Intellia Therapeutics
FMP Stock News
Original source text
Key Takeaways NTLA posted a narrower Q1 loss as research and development costs fell, though revenues declined 9.5% y/y.NTLA resumed phase III nex-z studies after the FDA lifted clinical holds in ATTR-CM and ATTRv-PN.Intellia began a rolling FDA filing for lonvo-z after phase III data showed 87% fewer HAE attacks. Intellia Therapeutics (NTLA - Free Report) incurred first-quarter 2026 loss of 81 cents per share, narrower than the Zacks Consensus Estimate of a loss of 92 cents. In the year-ago quarter, the company had incurred a loss of $1.10 per share.

Intellia’s total revenues currently comprise only collaboration revenues. The company reported revenues of $15 million for the first quarter of 2026, which missed the Zacks Consensus Estimate of $16 million. Total revenues declined 9.5% year over year.

Year to date, shares of NTLA have surged 60.4% against the industry’s 2.7% decline.

Image Source: Zacks Investment Research

NTLA’s Q1 Results in DetailResearch and development expenses totaled $80.7 million, down 25.5% from the year-ago quarter’s figure. The decrease was due to lower employee-related expenses, stock-based compensation and reduced spending on research materials and contracted services.

General and administrative expenses in the first quarter were $34.8 million, up 20.1% year over year, primarily due to continued investments in building the company’s commercial infrastructure and higher legal expenses, partially offset by lower stock-based compensation.

As of March 31, 2026, Intellia had cash, cash equivalents and marketable securities worth $517.2 million compared with $605.1 million as of Dec. 31, 2025.

Following an underwritten public offering of common stock, the company expects its cash runway to support operations into 2028.

NTLA's Recent Pipeline UpdatesIntellia has collaborated with Regeneron Pharmaceuticals (REGN - Free Report) to develop its investigational in vivo genome-editing candidate, nexiguran ziclumeran (nex-z), which is being studied for two indications — ATTR amyloidosis with polyneuropathy (ATTRv-PN) and ATTR amyloidosis with cardiomyopathy (ATTR-CM).

In March, the FDA lifted the clinical hold on the investigational new drug application (IND) for the phase III MAGNITUDE study evaluating nex-z in patients with ATTR-CM.

Earlier this year, the FDA lifted the clinical hold on the IND application for the phase III study, MAGNITUDE-2, evaluating nex-z in patients with ATTRv-PN. Enrollment in this study is expected to be completed in the second half of 2026.

With the removal of the clinical hold, Intellia is now focusing on completing patient enrollment in both late-stage studies as promptly as possible.

In April, Intellia announced top-line data from the global phase III HAELO study evaluating lonvo-z, an in vivo CRISPR gene editing therapy, for the treatment of hereditary angioedema (HAE). The study met its primary endpoint and all key secondary endpoints.

The study demonstrated that a one-time infusion of lonvo-z reduced HAE attacks by 87% compared with placebo over the six-month evaluation period. Patients treated with lonvo-z had a much lower average monthly attack rate (0.26) versus 2.10 in the placebo group. Per data, the company initiated a rolling submission of a biologics license application (BLA) to the FDA seeking approval for lonvo-z for the treatment of HAE.

The company expects to complete the BLA submission in the second half of 2026. Intellia plans to commercially launch lonvo-z in the first half of 2027, as the world’s first in vivo CRISPR-based gene editing therapy, if approved.

NTLA’s Zacks Rank & Stocks to ConsiderIntellia currently carries a Zacks Rank #3 (Hold).

Some better-ranked stocks in the biotech sector are Amarin Corporation (AMRN - Free Report) and Indivior Pharmaceuticals (INDV - Free Report) , both currently sporting a Zacks Rank #1 (Strong Buy). You can see the complete list of today’s Zacks #1 Rank stocks here.

Over the past 60 days, estimates for Amarin’s 2026 loss per share have narrowed from $7.01 to $6.36. Over the same period, loss per share estimates for 2027 have also narrowed from $5.50 to $4.64. AMRN shares have risen 7.6% year to date.

Amarin’s earnings beat estimates in three of the trailing four quarters and missed in the remaining one, with the average surprise being 50.02%.

Over the past 60 days, estimates for Indivior Pharmaceuticals’ 2026 earnings per share have increased from $3.03 to $3.35. Over the same period, EPS estimates for 2027 have risen to $3.69 from $3.46. INDV shares have risen 8.2% year to date.

Indivior Pharmaceuticals’ earnings beat estimates in each of the trailing four quarters, with the average surprise being 65.44%.
2026-06-12 11:47 1mo ago
2026-05-12 21:40 2mo ago
Intellia Therapeutics, Inc. (NTLA) Presents at Bank of America Global Healthcare Conference 2026 Transcript
NTLA Intellia Therapeutics
FMP Stock News
Original source text
Intellia Therapeutics, Inc. (NTLA) Presents at Bank of America Global Healthcare Conference 2026 Transcript
2026-06-12 11:47 1mo ago
2026-05-19 12:56 2mo ago
Can Intellia's Pipeline Push Drive Long-Term Growth Amid Rivalry?
NTLA Intellia Therapeutics
FMP Stock News
Original source text
Key Takeaways Intellia advanced phase III studies for nex-z in ATTR amyloidosis after the FDA lifted clinical holds.NTLA said the phase III HAELO study for lonvo-z met primary and key secondary endpoints.Intellia plans a 2027 launch for lonvo-z, pending FDA approval after completing BLA submission. Intellia Therapeutics (NTLA - Free Report) has been making decent progress with the advancement of its two pipeline candidates, nex-z (or, NTLA-2001) for transthyretin (ATTR) amyloidosis and lonvo-z (or NTLA-2002) for hereditary angioedema (HAE).

Intellia is developing nex-z in collaboration with Regeneron Pharmaceuticals (REGN - Free Report) . The candidate is being evaluated in two late-stage studies, MAGNITUDE and MAGNITUDE-2, for ATTR amyloidosis with cardiomyopathy (ATTR-CM) and ATTR amyloidosis with polyneuropathy (ATTRv-PN), respectively.

While NTLA is the lead party in the deal for nex-z, REGN shares 25% of the development costs and commercial profits. The company’s top line currently comprises only collaboration revenues from its partners, like Regeneron and others.

In March, the FDA lifted the clinical hold on the investigational new drug (IND) application for the phase III MAGNITUDE study evaluating nex-z in patients with ATTR-CM.

Earlier this year, the FDA lifted the clinical hold on the IND application for the phase III study, MAGNITUDE-2, evaluating nex-z in patients with ATTRv-PN. Enrollment in this study is expected to be completed in the second half of 2026.

Intellia is now focusing on completing patient enrollment in both late-stage studies as promptly as possible. The successful development of nex-z could provide impetus to the stock and create long-term growth visibility.

Meanwhile, last month, Intellia announced that the phase III HAELO study evaluating lonvo-z, an in vivo CRISPR gene editing therapy, for the treatment of HAE, has met its primary endpoint and all key secondary endpoints.

Simultaneously, NTLA initiated a rolling submission of a biologics license application (BLA) to the FDA seeking approval for lonvo-z for the treatment of HAE. The company expects to complete the BLA submission in the second half of 2026. Intellia plans to commercially launch lonvo-z in the first half of 2027, upon potential approval.

The successful development of its pipeline candidates will be a huge boost to Intellia. However, any regulatory or developmental setback related to ongoing studies will be a major setback. Growing competition in the target market also remains a worry.

NTLA's Competition in the Target MarketWhile Intellia’s pipeline of innovative CRISPR-based therapies appears promising, developing these candidates remains a complex and challenging process. Even if successfully developed and approved, the therapies are likely to face competition from other companies leveraging CRISPR/Cas9 gene-editing technology to target diseases across similar therapeutic areas.

CRISPR Therapeutics (CRSP - Free Report) is the first and only company in the world to market a CRISPR/Cas9-based therapy. CRSP’s one-shot gene therapy, Casgevy, was approved in late 2023 and early 2024 across the United States and Europe for two blood disorder indications — sickle cell disease and transfusion-dependent beta-thalassemia.

CRSP has developed Casgevy in partnership with large biotech, Vertex Pharmaceuticals, which is responsible for the therapy’s global development and commercialization.

Beam Therapeutics (BEAM - Free Report) is developing its leading ex-vivo genome-editing candidate, risto-cel, in the phase I/II BEACON study for the treatment of patients with SCD. BEAM plans to submit a BLA for risto-cel by the end of 2026.

Beam Therapeutics is also expanding its genetic disease pipeline by developing BEAM-301 and BEAM-302 for the treatment of glycogen storage disease type 1a and alpha-1 antitrypsin deficiency, respectively.

NTLA's Price Performance, Valuation and EstimatesYear to date, shares of Intellia have rallied 41.1% against the industry’s decline of 2.2%. The stock has also outperformed the sector and the S&P 500 during the same time frame, as seen in the chart below.

Image Source: Zacks Investment Research

From a valuation standpoint, Intellia is trading at a discount to the industry. Going by the price/book ratio, the company’s shares currently trade at 2.46, lower than 3.13 for the industry. The stock is trading below its five-year mean of 2.58.

Image Source: Zacks Investment Research

The Zacks Consensus Estimate for Intellia’s 2026 loss per share has narrowed from $3.53 to $3.35 over the past 30 days. Loss per share estimates for 2027 have widened from $1.22 to $1.54 during the same time frame.

Image Source: Zacks Investment Research

NTLA's Zacks RankIntellia currently has a Zacks Rank #3 (Hold). You can see the complete list of today’s Zacks #1 Rank (Strong Buy) stocks here.
2026-06-12 11:47 1mo ago
2026-05-27 15:36 1mo ago
ADMA vs Intellia Therapeutics: Which Biotech Stock Is a Better Pick Now?
NTLA Intellia Therapeutics
FMP Stock News
Original source text
Key Takeaways Intellia reported positive phase III data for lonvo-z and targets a 2027 U.S. launch. NTLA resumed nex-z phase III studies after the FDA lifted prior clinical holds in 2026. ADMA faced weaker Bivigam sales as pricing pressure and elevated IG inventories weighed on demand. ADMA Biologics (ADMA - Free Report) markets plasma-derived biologics for the treatment of immune deficiencies and the prevention of certain infectious diseases.

Intellia Therapeutics (NTLA - Free Report) is a biopharmaceutical company focused on advancing CRISPR gene-editing and related technologies to develop potentially curative therapies for severe diseases. Leveraging deep expertise in science, technology, and clinical development, the company aims to transform patient care by targeting the underlying causes of disease and redefining the future of medicine.

ADMA Biologics and Intellia Therapeutics operate in distinct areas of biotechnology, but they are comparable in terms of market capitalization, as both are generally viewed as small- to mid-cap biotech companies.

Hence, let us delve into their fundamentals, growth prospects, challenges and valuation levels to make a prudent choice.  

The Case for ADMA Biologics  ADMA Biologics markets plasma-derived biologics for the treatment of immune deficiencies and the prevention of certain infectious diseases.

The company’s top line currently comprises sales of three FDA-approved products — Bivigam (an Intravenous Immune Globulin [“IVIG”] product to treat primary humoral immunodeficiency), Asceniv (to treat primary immunodeficiency disease or PIDD) and Nabi-HB (to treat and provide enhanced immunity against the hepatitis B virus).

However, ADMA is currently grappling with macro challenges in the immunoglobulin (IG) products market.  

Total revenues in the first quarter were $114.5 million, down 0.3% from the year-ago quarter’s level. Bivigam revenues declined 54% year over year.  

Management noted that increased competition, elevated channel inventories and aggressive pricing activity in standard IG products created temporary pressure on top-line performance, particularly for Bivigam.

Late-quarter inventory shifts pushed certain contractual purchase orders expected in March into early April, affecting the timing of reported revenues. The company said these delays were partly due to temporary shortages in required safety stock levels at some customers and were resolved within the applicable cure period.

Asceniv, its lead product, is a plasma-derived IVIG that contains naturally occurring polyclonal antibodies. It remained the key contributor to ADMA’s revenue performance, while the company’s other product lines trended in the opposite direction. 

Asceniv recorded 28% year-over-year revenue growth, driven by record utilization, expanding prescriber adoption, strong patient adherence and continued new patient starts.

ADMA emphasized that underlying Asceniv demand remained strong, citing record utilization growth, record new patient starts, expanding prescriber breadth and steady patient adherence. ADMA also noted that April demand supported a second-quarter run rate consistent with first-quarter direct sales, giving early signs of normalization in ordering patterns.  

ADMA continued progressing SG-001, its hyperimmune globulin program targeting S. pneumoniae. Management reiterated a capital-efficient approach to development and believes the program could represent a meaningful long-term opportunity, citing an estimated $300 million to $500 million annual market opportunity if approved.

The Case for NTLA  Intellia Therapeutics represents a high-growth biotechnology company with significant upside potential driven by its leadership in CRISPR-based gene-editing therapies. The company has spent more than a decade developing proprietary technologies, including gene editing, oligonucleotides and lipid nanoparticle delivery systems, to advance first-in-class treatments for severe diseases.

Its lead candidates, lonvoguran ziclumeran (lonvo-z) for hereditary angioedema (HAE) and nexiguran ziclumeran for ATTR amyloidosis, are the first in vivo genome-editing therapies to enter phase III development. These one-time intravenous treatments target diseases with high unmet need and could potentially offer durable or curative benefits, creating a large commercial opportunity if approved.

Lonvoguran ziclumeran is an investigational one-time CRISPR-based therapy developed by NTLA to treat HAE by permanently reducing kallikrein production in the liver, with the goal of dramatically lowering or eliminating HAE attacks.

In the phase III HAELO study, lonvo-z achieved positive top-line results, reducing HAE attacks by 87% versus placebo and meeting all key secondary endpoints with strong statistical significance. The therapy also demonstrated favorable safety and tolerability, with no serious adverse events reported. Following these results, NTLA initiated a rolling BLA submission to the FDA, targeting a potential launch in the first half of 2027 in the United States.  

NTLA’s other candidate, nexiguran ziclumeran (nex-z) is an investigational one-time CRISPR-based therapy designed to silence the TTR gene in the liver, potentially halting or reversing ATTR amyloidosis through durable reduction of TTR protein levels.

The company faced a temporary setback in late 2025 after a patient death led the FDA to place clinical holds on the phase III MAGNITUDE studies on nex-z. However, the FDA lifted both holds in early 2026, allowing patient screening to resume. Nex-z is being co-developed with Regeneron Pharmaceuticals, which shares development costs and future commercial profits under the collaboration agreement.

The successful development and commercialization of these candidates could position Intellia as a pioneer in the emerging gene-editing market and significantly expand its long-term revenue potential. Intellia ended the first quarter of 2026 with $517.2 million in cash, cash equivalents, and marketable securities.

The company further strengthened its balance sheet through a public stock offering in April 2026 that generated approximately $207 million in gross proceeds. Management expects its current cash reserves to fund operations into 2028, extending well beyond the anticipated U.S. commercial launch of lonvo-z in the first half of 2027.  

A Look at Estimates: ADMA vs NTLA  The Zacks Consensus Estimate for ADMA’s 2026 sales implies a year-over-year increase of 5.86%, and that for earnings per share (EPS) suggests an improvement of 40%.  However, EPS estimates for 2026 and 2027 have moved south in the past 60 days.  

ADMA’s Estimate Movement  
Image Source: Zacks Investment Research

The Zacks Consensus Estimate for NTLA’s 2026 sales implies a year-over-year decrease of 7.75%, while that for EPS suggests an improvement of 13.65%. Loss estimates for both 2026 and 2027 have narrowed in the past 60 days.  

NTLA Estimate Movement
Image Source: Zacks Investment Research

Price Performance and Valuation of ADMA and NTLAFrom a price-performance perspective, NTLA has performed well so far this year versus ADMA. Shares of ADMA have plunged 55.3%. In contrast, NTLA shares have surged 40.3%. The industry has declined 0.5% in the said period.  

Image Source: Zacks Investment Research

From a valuation standpoint, ADMA’s shares currently trade at 3.19X forward sales, lower than 9.71X for NTLA.  

Image Source: Zacks Investment Research

Which Stock Is a Better Pick for Now?  ADMA currently has a Zacks Rank #5 (Strong Sell) while NTLA carries a Zacks Rank #3 (Hold).  

You can see the complete list of today’s Zacks #1 Rank (Strong Buy) stocks here.

Although demand for ADMA’s Asceniv continues to be solid, broader pressure across the U.S. plasma-derived products space suggests a more cautious near-term outlook. Competitive intensity, pricing dynamics and market share concerns could continue to weigh on growth visibility and margin expansion prospects.  

In contrast, Intellia is a clinical-stage biotechnology company developing CRISPR-based gene-editing therapies designed to potentially cure severe diseases by targeting their underlying genetic causes. NTLA strengthened its investment case after reporting positive phase III top-line data for lonvo-z in April 2026, with a commercial launch planned for the first half of 2027. Successful commercialization could position Intellia as a pioneer in the emerging gene-editing market and significantly expand its long-term revenue potential.

Hence, we prefer NTLA over ADMA, given its significant growth opportunity in genetic medicine and the recent positive revisions to earnings estimates.
2026-06-12 11:47 1mo ago
2026-05-31 08:45 1mo ago
Intellia Therapeutics - Steady Progress, Historic Commercial Approval In Sight
NTLA Intellia Therapeutics
FMP Stock News
Original source text
Intellia Therapeutics remains a Buy, driven by two pivotal in vivo gene therapy catalysts: Lonvo-Z for HAE and Nex-Z for ATTR amyloidosis. Lonvo-Z's Phase 3 data met all endpoints with an 87% attack reduction, but market reaction was muted due to safety concerns and the competitive landscape. The FDA lifted clinical holds on Nex-Z Phase 3 trials, enabling advancement in a $16.8bn ATTR market with a differentiated one-time treatment profile.
2026-06-12 11:47 1mo ago
2026-06-01 07:30 1mo ago
Intellia Therapeutics to Report Additional Phase 3 HAELO Data for Lonvoguran Ziclumeran (lonvo-z) in Late-Breaking Oral Presentation at EAACI 2026
NTLA Intellia Therapeutics
FMP Stock News
Original source text
June 01, 2026 07:30 ET  | Source: Intellia Therapeutics, Inc.

CAMBRIDGE, Mass., June 01, 2026 (GLOBE NEWSWIRE) -- Intellia Therapeutics, Inc. (Nasdaq: NTLA), a leading biopharmaceutical company focused on revolutionizing medicine leveraging CRISPR gene editing and other core technologies, today announced that data from the global Phase 3 HAELO clinical trial of lonvo-z (formerly known as NTLA-2002) in hereditary angioedema (HAE) will be presented in a late-breaking oral presentation at the European Academy of Allergy & Clinical Immunology (EAACI) Annual Congress 2026, taking place June 12-15 in Istanbul, Türkiye. Intellia will also have a poster presentation detailing the burdens experienced by HAE patients living outside the United States.

Late-Breaking Oral Presentation Details:

Title: HAELO, a Phase 3, Global, Randomised, Double-Blind, Placebo-Controlled Study of Lonvoguran Ziclumeran, a CRISPR-Based Gene Editing Therapy, in Patients with Hereditary Angioedema
Session: Immune deficiencies and autoimmunity
Data and Time: Saturday, June 13, 2026, from 8:45 – 9:45 a.m. TRT
Presentation Number: 100217
Presenter: Danny Cohn, M.D., Ph.D., Internist, Department of Vascular Medicine, Amsterdam Cardiovascular Sciences, Amsterdam University Medical Center, University of Amsterdam Poster Presentation Details:

Title: Barriers to Normalization with Existing Treatments Among People Living with Hereditary Angioedema in Europe
Session: Immune deficiencies and autoimmunity 02
Data and Time: Friday, June 12, 2026, from 12:00 – 1:00 p.m. TRT
Poster Number: D1.336
Presenter: Henriette Farkas, M.D., Ph.D., Professor of Allergy and Clinical Immunology Director of the Hungarian Angioedema Center of Reference and Excellence, Department of Internal Medicine and Hematology, Semmelweis University About Lonvo-z
Based on Nobel Prize-winning CRISPR/Cas9 technology, lonvo-z has the potential to become the first one-time treatment for hereditary angioedema (HAE). Lonvo-z is an in vivo CRISPR gene editing candidate that is intended to permanently lower kallikrein by inactivating the kallikrein B1 (KLKB1) gene with a single dose. Lonvo-z has received five notable regulatory designations: Orphan Drug and RMAT Designation by the U.S. Food and Drug Administration (FDA), the Innovation Passport by the U.K. Medicines and Healthcare products Regulatory Agency (MHRA), Priority Medicines (PRIME) Designation by the European Medicines Agency, as well as Orphan Drug Designation (ODD) by the European Commission.

About Hereditary Angioedema
Hereditary angioedema (HAE) is a rare, genetic disease characterized by severe, recurring and unpredictable inflammatory attacks in various organs and tissues of the body, which can be painful, debilitating and life-threatening. It is estimated that one in 50,000 people are affected by HAE. There are preventative and on-demand treatment options to help manage the condition, including long- and short-term prophylaxis used to prevent swelling attacks. Current treatment options often include lifelong therapies, which may require chronic intravenous (IV) or subcutaneous (SC) administration as often as twice per week or daily oral administration to ensure constant pathway suppression for disease control. Despite chronic administration, breakthrough attacks still occur. Kallikrein inhibition is a clinically validated strategy for the preventive treatment of HAE attacks.

About Intellia Therapeutics
Intellia Therapeutics, Inc. (Nasdaq: NTLA) is a leading clinical-stage biopharmaceutical company focused on revolutionizing medicine leveraging CRISPR gene editing and other core technologies. The company’s mission is to transform the lives of people with severe diseases by developing and commercializing potentially curative treatments. With deep scientific, technical and clinical development experience, Intellia aims to reset the standard for medicine by durably treating the root causes of disease. Learn more at intelliatx.com and follow us @intelliatx.

Investor Contact:
Jason Fredette
Vice President, Investor Relations and Corporate Communications
Intellia Therapeutics, Inc.
[email protected]

Media Contact:
Mike Tattory
Vice President
LifeSci Communications
[email protected] 
2026-06-12 11:47 1mo ago
2026-06-05 16:05 1mo ago
Intellia Therapeutics Reports Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)
NTLA Intellia Therapeutics
FMP Stock News
Original source text
June 05, 2026 16:05 ET  | Source: Intellia Therapeutics, Inc.

CAMBRIDGE, Mass., June 05, 2026 (GLOBE NEWSWIRE) -- Intellia Therapeutics, Inc. (Nasdaq: NTLA), a leading biopharmaceutical company focused on revolutionizing medicine leveraging CRISPR gene editing and other core technologies, today announced that on June 1, 2026, it awarded inducement grants to six new employees under Intellia’s 2024 Inducement Plan, as amended, as a material inducement to employment.

The inducement grants consisted of time-based restricted stock units (“RSUs”) for an aggregate of 47,150 shares of Intellia’s common stock, with one-third of such RSUs vesting annually over three years. All equity vesting is subject to each employee’s continued service as an employee of, or other service provider to, Intellia through the applicable vesting dates.

All of the above-described awards were granted outside of Intellia’s stockholder-approved equity incentive plans pursuant to Intellia’s 2024 Inducement Plan, as amended, which was initially adopted by the board of directors in June 2024. These awards were approved by Intellia’s compensation committee as a material inducement to entering into employment with Intellia in accordance with Nasdaq Listing Rule 5635(c)(4).

About Intellia Therapeutics

Intellia Therapeutics, Inc. (Nasdaq: NTLA) is a leading clinical-stage biopharmaceutical company focused on revolutionizing medicine leveraging CRISPR gene editing and other core technologies. The company’s mission is to transform the lives of people with severe diseases by developing and commercializing potentially curative treatments. With deep scientific, technical and clinical development experience, Intellia aims to reset the standard for medicine by durably treating the root causes of disease. Learn more at intelliatx.com and follow us @intelliatx.

Investor Contact:
Jason Fredette
Vice President, Investor Relations and Corporate Communications
Intellia Therapeutics, Inc.
[email protected]

Media Contact:
Mike Tattory
Vice President
LifeSci Communications
[email protected]
2026-06-12 11:47 1mo ago
2026-06-10 12:31 1mo ago
Intellia Therapeutics (NTLA) Down 7.9% Since Last Earnings Report: Can It Rebound?
NTLA Intellia Therapeutics
FMP Stock News
Original source text
A month has gone by since the last earnings report for Intellia Therapeutics, Inc. (NTLA - Free Report) . Shares have lost about 7.9% in that time frame, underperforming the S&P 500.

Will the recent negative trend continue leading up to its next earnings release, or is Intellia Therapeutics due for a breakout? Well, first let's take a quick look at its most recent earnings report in order to get a better handle on the recent drivers for Intellia Therapeutics, Inc. before we dive into how investors and analysts have reacted as of late.

Intellia Q1 Earnings Beat Estimates, Revenues Miss MarkIntellia incurred a first-quarter 2026 loss of 81 cents per share, narrower than the Zacks Consensus Estimate of a loss of 92 cents. In the year-ago quarter, the company had incurred a loss of $1.10 per share.

Intellia’s total revenues currently comprise only collaboration revenues. The company reported revenues of $15 million for the first quarter of 2026, which missed the Zacks Consensus Estimate of $16 million. Total revenues declined 9.5% year over year.

Quarter in DetailResearch and development expenses totaled $80.7 million, down 25.5% from the year-ago quarter’s figure. The decrease was due to lower employee-related expenses, stock-based compensation and reduced spending on research materials and contracted services.

General and administrative expenses in the first quarter were $34.8 million, up 20.1% year over year, primarily due to continued investments in building the company’s commercial infrastructure and higher legal expenses, partially offset by lower stock-based compensation.

As of March 31, 2026, Intellia had cash, cash equivalents and marketable securities worth $517.2 million compared with $605.1 million as of Dec. 31, 2025.

Following an underwritten public offering of common stock, the company expects its cash runway to support operations into 2028.

How Have Estimates Been Moving Since Then?In the past month, investors have witnessed a upward trend in estimates revision.

The consensus estimate has shifted 7.62% due to these changes.

VGM ScoresAt this time, Intellia Therapeutics has a average Growth Score of C, however its Momentum Score is doing a lot better with an A. However, the stock has a grade of F on the value side, putting it in the fifth quintile for value investors.

Overall, the stock has an aggregate VGM Score of D. If you aren't focused on one strategy, this score is the one you should be interested in.

OutlookEstimates have been broadly trending upward for the stock, and the magnitude of these revisions looks promising. Notably, Intellia Therapeutics has a Zacks Rank #3 (Hold). We expect an in-line return from the stock in the next few months.

Performance of an Industry PlayerIntellia Therapeutics belongs to the Zacks Medical - Biomedical and Genetics industry. Another stock from the same industry, Incyte (INCY - Free Report) , has gained 4.1% over the past month. More than a month has passed since the company reported results for the quarter ended March 2026.

Incyte reported revenues of $1.27 billion in the last reported quarter, representing a year-over-year change of +20.9%. EPS of $1.81 for the same period compares with $1.16 a year ago.

Incyte is expected to post earnings of $1.80 per share for the current quarter, representing a year-over-year change of +14.7%. Over the last 30 days, the Zacks Consensus Estimate has changed -3.3%.

Incyte has a Zacks Rank #3 (Hold) based on the overall direction and magnitude of estimate revisions. Additionally, the stock has a VGM Score of B.
2026-06-12 11:46 1mo ago
2026-03-22 02:47 4mo ago
Arlo Technologies General Counsel Sells 25000 Shares for $352000 to Cover Taxes
ARLO Arlo
FMP Stock News
Original source text
Brian Busse, General Counsel of Arlo Technologies (ARLO +3.17%), reported the sale of 25,525 direct shares for approximately $352K following the addition of shares on March 12, 2026, according to a SEC Form 4 filing.

Transaction summaryMetricValueShares sold (direct)25,525Transaction value~$352KPost-transaction shares (direct)583,364Post-transaction value (direct ownership)~$7.88 millionTransaction value based on SEC Form 4 weighted average purchase price ($13.78); post-transaction value based on March 12, 2026 market close ($13.78).

Key questionsWhat is the context of this trade?
The sale of 25,525 shares followed Busse’s addition of 50,000 shares under a performance stock unit (PSU) plan. The sale of shares was only conducted to satisfy estimated tax withholding obligations. How significant is the reduction in ownership as a result of this sale?
The transaction reduced Busse's direct holdings by 4.19%, leaving him with 583,364 shares valued at approximately ~$7.88 million as of the transaction date. Company overviewMetricValueMarket capitalization$1.53 billionRevenue (TTM)$529.30 millionNet income (TTM)$14.93 million1-year price change (as of 3/21/26)32%

Today's Change

(

3.17

%) $

0.39

Current Price

$

12.71

Company snapshotArlo Technologies is a cloud-based platform that offers a portfolio of smart, connected security devices, including indoor and outdoor cameras, video doorbells, floodlight cameras, and accessories, all integrated with a proprietary cloud platform and mobile applications. Along with product sales, it has a subscription-based service model that drives recurring revenue and customer engagement. It targets residential and small-business customers seeking intelligent, cloud-enabled security and monitoring solutions across the Americas, Europe, the Middle East, Africa, and Asia.

What this transaction means for investorsIt’s important to emphasize that this sale was strictly to cover estimated taxes for the 50,000 PSUs that vested into shares on March 10, through Busse’s PSU plan with the company. And while having to sell over half the shares he gained for taxes, the general counsel member technically gained more shares than he lost when looking at the entire filing.

Arlo Technologies is less than a month removed from a very strong Q4 earnings report for its fiscal year of 2025. On Feb. 26, 2026, the company reported its first fiscal year of net income, after years of annual net losses. It also posted its largest year-over-year (YoY) increase in quarterly free cash flow since Q2 2021, with its 17.94 million in free cash flow being 220.59% higher than the previous year’s Q4.

The stock jumped in February 2026 after the strong postings, and it is up 2.57% so far this year. Early in March, the company announced a $50 million stock repurchase program, approved by its Board of Directors and set to continue through Dec. 31, 2027. This may help drive share prices even higher.

With strong financials and stock performance, Arlo Technologies looks like a considerable investment opportunity in the smart home security industry.
2026-06-12 11:46 1mo ago
2026-03-28 09:22 3mo ago
Arlo: Poised To Keep Rallying As Subscribers Grow
ARLO Arlo
FMP Stock News
Original source text
Arlo remains a compelling buy as small caps lag and market volatility persists, with fundamentals supporting upside. ARLO's ARR and paid subscriber base are growing over 20% y/y, driving EBITDA and free cash flow expansion. The company's improving margin profile and disciplined inventory management underpin its long-term growth thesis.
2026-06-12 11:46 1mo ago
2026-03-30 03:32 3mo ago
Arlo Technologies, Inc. (NYSE:ARLO) Receives $23.33 Average PT from Analysts
ARLO Arlo
FMP Stock News
Original source text
Posted by Defense World Staff on Mar 30th, 2026

Shares of Arlo Technologies, Inc. (NYSE:ARLO – Get Free Report) have received an average rating of “Moderate Buy” from the five research firms that are currently covering the firm, Marketbeat Ratings reports. Two investment analysts have rated the stock with a hold rating and three have assigned a buy rating to the company. The average 1 year price target among brokers that have covered the stock in the last year is $23.3333.

ARLO has been the topic of a number of research reports. Weiss Ratings upgraded Arlo Technologies from a “sell (d+)” rating to a “hold (c-)” rating in a report on Friday, March 6th. Zacks Research downgraded shares of Arlo Technologies from a “strong-buy” rating to a “hold” rating in a research report on Tuesday, January 6th.

View Our Latest Research Report on Arlo Technologies

Arlo Technologies Stock Up 0.3% ARLO opened at $13.50 on Friday. The firm has a market capitalization of $1.44 billion, a P/E ratio of 103.84 and a beta of 1.65. The stock has a fifty day moving average of $13.24 and a 200-day moving average of $14.85. Arlo Technologies has a 12-month low of $7.84 and a 12-month high of $19.94.

Arlo Technologies (NYSE:ARLO – Get Free Report) last posted its quarterly earnings results on Thursday, February 26th. The company reported $0.22 earnings per share for the quarter, beating the consensus estimate of $0.16 by $0.06. The firm had revenue of $141.30 million for the quarter, compared to analyst estimates of $135.57 million. Arlo Technologies had a return on equity of 10.76% and a net margin of 2.82%.Arlo Technologies’s quarterly revenue was up 16.2% on a year-over-year basis. During the same period in the previous year, the firm earned $0.10 earnings per share. Arlo Technologies has set its Q1 2026 guidance at 0.170-0.230 EPS. On average, analysts expect that Arlo Technologies will post -0.29 earnings per share for the current fiscal year.

Arlo Technologies announced that its board has initiated a share repurchase program on Wednesday, March 4th that authorizes the company to repurchase $50.00 million in shares. This repurchase authorization authorizes the company to buy up to 3.1% of its stock through open market purchases. Stock repurchase programs are often an indication that the company’s leadership believes its shares are undervalued.

Insider Activity In other news, General Counsel Brian Busse sold 31,407 shares of the business’s stock in a transaction on Friday, February 6th. The shares were sold at an average price of $12.29, for a total transaction of $385,992.03. Following the transaction, the general counsel directly owned 552,850 shares in the company, valued at $6,794,526.50. The trade was a 5.38% decrease in their position. The transaction was disclosed in a legal filing with the SEC, which is available at this link. Also, CEO Matthew Blake Mcrae sold 153,433 shares of the company’s stock in a transaction on Thursday, March 12th. The stock was sold at an average price of $13.78, for a total transaction of $2,114,306.74. Following the completion of the transaction, the chief executive officer directly owned 1,168,866 shares in the company, valued at $16,106,973.48. This trade represents a 11.60% decrease in their ownership of the stock. The SEC filing for this sale provides additional information. Insiders have sold a total of 842,522 shares of company stock worth $11,321,821 in the last ninety days. Corporate insiders own 5.20% of the company’s stock.

Institutional Investors Weigh In On Arlo Technologies A number of hedge funds and other institutional investors have recently made changes to their positions in ARLO. AQR Capital Management LLC grew its stake in shares of Arlo Technologies by 28.8% in the 1st quarter. AQR Capital Management LLC now owns 406,688 shares of the company’s stock valued at $4,014,000 after buying an additional 90,970 shares in the last quarter. MIRAE ASSET GLOBAL ETFS HOLDINGS Ltd. lifted its stake in Arlo Technologies by 15.5% in the first quarter. MIRAE ASSET GLOBAL ETFS HOLDINGS Ltd. now owns 171,986 shares of the company’s stock valued at $1,698,000 after acquiring an additional 23,068 shares during the last quarter. Millennium Management LLC lifted its stake in Arlo Technologies by 116.1% in the first quarter. Millennium Management LLC now owns 455,692 shares of the company’s stock valued at $4,498,000 after acquiring an additional 244,783 shares during the last quarter. Goldman Sachs Group Inc. grew its position in Arlo Technologies by 115.1% in the first quarter. Goldman Sachs Group Inc. now owns 1,552,652 shares of the company’s stock worth $15,325,000 after acquiring an additional 830,770 shares in the last quarter. Finally, Jane Street Group LLC increased its stake in shares of Arlo Technologies by 279.8% during the 1st quarter. Jane Street Group LLC now owns 292,302 shares of the company’s stock worth $2,885,000 after purchasing an additional 215,343 shares during the last quarter. 83.18% of the stock is owned by hedge funds and other institutional investors.

Arlo Technologies Company Profile (Get Free Report)

Arlo Technologies, Inc (NYSE: ARLO) is a provider of smart home security products and services designed for residential and small business customers. The company offers a portfolio of wireless and Wi-Fi-enabled security cameras, video doorbells, smart lighting solutions, and associated accessories. Arlo integrates advanced video analytics, motion detection, cloud storage, and two-way audio capabilities to deliver end-to-end security and monitoring solutions accessible through mobile applications and web interfaces.

Founded as a division of Netgear, Inc in 2014 and spun off as an independent public company in 2018, Arlo Technologies has established a presence in North America, Europe, Australia and parts of Asia.

Featured Stories Five stocks we like better than Arlo Technologies

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2026-06-12 11:46 1mo ago
2026-04-08 02:15 3mo ago
Comparing Riskified (NYSE:RSKD) & Arlo Technologies (NYSE:ARLO)
ARLO Arlo
FMP Stock News
Original source text
Posted by Defense World Staff on Apr 8th, 2026

Riskified (NYSE:RSKD – Get Free Report) and Arlo Technologies (NYSE:ARLO – Get Free Report) are both small-cap computer and technology companies, but which is the superior stock? We will contrast the two businesses based on the strength of their risk, profitability, institutional ownership, valuation, earnings, analyst recommendations and dividends.

Profitability This table compares Riskified and Arlo Technologies’ net margins, return on equity and return on assets.

Net Margins Return on Equity Return on Assets Riskified -8.00% -5.63% -4.24% Arlo Technologies 2.82% 10.76% 4.03% Analyst Ratings This is a summary of current recommendations for Riskified and Arlo Technologies, as provided by MarketBeat.com.

Sell Ratings Hold Ratings Buy Ratings Strong Buy Ratings Rating Score Riskified 1 3 3 0 2.29 Arlo Technologies 0 2 3 0 2.60 Riskified currently has a consensus target price of $5.96, indicating a potential upside of 45.79%. Arlo Technologies has a consensus target price of $23.33, indicating a potential upside of 64.96%. Given Arlo Technologies’ stronger consensus rating and higher possible upside, analysts plainly believe Arlo Technologies is more favorable than Riskified.

Institutional & Insider Ownership 59.0% of Riskified shares are owned by institutional investors. Comparatively, 83.2% of Arlo Technologies shares are owned by institutional investors. 17.4% of Riskified shares are owned by company insiders. Comparatively, 5.2% of Arlo Technologies shares are owned by company insiders. Strong institutional ownership is an indication that hedge funds, endowments and large money managers believe a company will outperform the market over the long term.

Earnings and Valuation This table compares Riskified and Arlo Technologies”s revenue, earnings per share and valuation.

Gross Revenue Price/Sales Ratio Net Income Earnings Per Share Price/Earnings Ratio Riskified $344.64 million 1.76 -$27.57 million ($0.17) -24.04 Arlo Technologies $529.30 million 2.86 $14.93 million $0.13 108.81 Arlo Technologies has higher revenue and earnings than Riskified. Riskified is trading at a lower price-to-earnings ratio than Arlo Technologies, indicating that it is currently the more affordable of the two stocks.

Volatility and Risk Riskified has a beta of 1.33, indicating that its stock price is 33% more volatile than the S&P 500. Comparatively, Arlo Technologies has a beta of 1.71, indicating that its stock price is 71% more volatile than the S&P 500.

Summary Arlo Technologies beats Riskified on 12 of the 13 factors compared between the two stocks.

About Riskified (Get Free Report)

Riskified Ltd., together with its subsidiaries, develops and offers an e-commerce risk management platform that allows online merchants to create trusted relationships with consumers in the United States, Europe, the Middle East, Africa, the Asia-Pacific, and the Americas. It offers Chargeback Guarantee that ensures the legitimacy of merchants' online orders; Policy Protect, a machine learning solution designed to detect and prevent refund and returns policy abuse in real-time; Account Secure, a solution that cross-checks every login attempt; Dispute Resolve, which is used to compile submissions for fraud and non-fraud related chargeback issues; and PSD2 Optimize that helps merchants avoid bank authorization failures and abandoned shopping carts. The company serves direct-to-consumer brands, online-only retailers, omnichannel retailers, online marketplaces, and e-commerce service providers in various industries, such as payments, money transfer and crypto, tickets and travel, electronics, home, and fashion and luxury goods. Riskified Ltd. was incorporated in 2012 and is headquartered in Tel Aviv, Israel.

About Arlo Technologies (Get Free Report)

Arlo Technologies, Inc., together with its subsidiaries, provides a cloud-based platform in the Americas, Europe, the Middle East, Africa, and the Asia Pacific regions. The company offers Arlo Essential Cameras and Doorbells (2nd Generation) delivers smart home protection, including automated privacy shield, 180-degree field of view, and 2K video resolution; Arlo Home Security System, an all-in-one multi-sensor that provides access to security experts for monitoring and responding to emergency situations; Arlo Pro 5S, a wireless 2K video resolution security camera; Arlo Go 2, a camera for monitoring remote areas, large properties, construction sites, vacation homes, boat or RV slips, and hard-to-access areas; Arlo Ultra 2 provides 4K video with HDR, an ultra-wide, 180-degree field of view, auto zoom and tracking on moving objects, and color night vision; and Arlo Floodlight Camera, a wire-free floodlight camera. It provides security system accessories, charging accessories, and mounts. In addition, the company offers Arlo Secure subscriptions, including emergency response secure plus plan; 2K secure plan and 4K secure plus plan cloud-based video recording; unlimited cameras; advanced object detection; smart interactive notifications; smoke and CO alarm detection; cloud-based activity zone; call a friend; and 24/7 priority support and professional monitoring services; Arlo Total Security, a subscription which provides 24/7 professional monitoring and security hardware; Arlo Safe, a personal safety app that offers one-touch emergency response, family safety, and crash detection and response services; and Arlo SmartCloud, a SaaS solution that delivers security cloud services for business. It sells its products through retailers, wholesale distributors, broadcast channels, wireless carriers, and security solution providers, as well as through its website. Arlo Technologies, Inc. was incorporated in 2018 and is headquartered in Carlsbad, California.

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2026-06-12 11:46 1mo ago
2026-04-09 04:02 3mo ago
Kurtis Joseph Binder Sells 25,000 Shares of Arlo Technologies (NYSE:ARLO) Stock
ARLO Arlo
FMP Stock News
Original source text
Posted by Defense World Staff on Apr 9th, 2026

Arlo Technologies, Inc. (NYSE:ARLO – Get Free Report) CFO Kurtis Joseph Binder sold 25,000 shares of the firm’s stock in a transaction dated Monday, April 6th. The stock was sold at an average price of $13.99, for a total value of $349,750.00. Following the sale, the chief financial officer directly owned 589,885 shares in the company, valued at $8,252,491.15. This trade represents a 4.07% decrease in their position. The sale was disclosed in a filing with the SEC, which is accessible through this link. The transaction was executed under a pre-arranged Rule 10b5-1 trading plan.

Kurtis Joseph Binder also recently made the following trade(s):

On Thursday, March 12th, Kurtis Joseph Binder sold 179,419 shares of Arlo Technologies stock. The stock was sold at an average price of $13.78, for a total value of $2,472,393.82. On Wednesday, March 4th, Kurtis Joseph Binder sold 9,665 shares of Arlo Technologies stock. The stock was sold at an average price of $15.11, for a total value of $146,038.15. On Tuesday, March 3rd, Kurtis Joseph Binder sold 12,539 shares of Arlo Technologies stock. The stock was sold at an average price of $14.93, for a total value of $187,207.27. On Friday, January 9th, Kurtis Joseph Binder sold 55,043 shares of Arlo Technologies stock. The stock was sold at an average price of $13.69, for a total value of $753,538.67. Arlo Technologies Stock Performance Shares of NYSE ARLO opened at $13.60 on Thursday. Arlo Technologies, Inc. has a fifty-two week low of $8.37 and a fifty-two week high of $19.94. The firm has a market capitalization of $1.45 billion, a PE ratio of 104.62 and a beta of 1.71. The stock’s 50-day simple moving average is $13.32 and its 200-day simple moving average is $14.66.

Arlo Technologies (NYSE:ARLO – Get Free Report) last issued its earnings results on Friday, February 27th. The company reported $0.22 earnings per share for the quarter, topping the consensus estimate of $0.16 by $0.06. The business had revenue of $141.30 million for the quarter, compared to analyst estimates of $135.57 million. Arlo Technologies had a return on equity of 10.76% and a net margin of 2.82%.The business’s quarterly revenue was up 16.2% on a year-over-year basis. During the same quarter last year, the company earned $0.10 EPS. On average, sell-side analysts forecast that Arlo Technologies, Inc. will post -0.29 earnings per share for the current fiscal year.

Arlo Technologies declared that its board has initiated a share repurchase program on Wednesday, March 4th that permits the company to buyback $50.00 million in outstanding shares. This buyback authorization permits the company to buy up to 3.1% of its stock through open market purchases. Stock buyback programs are often a sign that the company’s leadership believes its stock is undervalued.

Institutional Inflows and Outflows Several hedge funds and other institutional investors have recently modified their holdings of the stock. Arizona State Retirement System grew its stake in shares of Arlo Technologies by 2.3% in the 3rd quarter. Arizona State Retirement System now owns 30,597 shares of the company’s stock valued at $519,000 after purchasing an additional 702 shares during the last quarter. Smartleaf Asset Management LLC grew its stake in shares of Arlo Technologies by 86.0% in the 3rd quarter. Smartleaf Asset Management LLC now owns 1,616 shares of the company’s stock valued at $28,000 after purchasing an additional 747 shares during the last quarter. Quarry LP grew its stake in shares of Arlo Technologies by 42.0% in the 3rd quarter. Quarry LP now owns 2,649 shares of the company’s stock valued at $45,000 after purchasing an additional 783 shares during the last quarter. Oregon Public Employees Retirement Fund grew its stake in shares of Arlo Technologies by 3.4% in the 4th quarter. Oregon Public Employees Retirement Fund now owns 24,268 shares of the company’s stock valued at $340,000 after purchasing an additional 800 shares during the last quarter. Finally, Farther Finance Advisors LLC grew its stake in shares of Arlo Technologies by 12.5% in the 4th quarter. Farther Finance Advisors LLC now owns 7,631 shares of the company’s stock valued at $107,000 after purchasing an additional 849 shares during the last quarter. 83.18% of the stock is currently owned by hedge funds and other institutional investors.

Analyst Ratings Changes A number of research analysts recently issued reports on ARLO shares. Zacks Research downgraded Arlo Technologies from a “strong-buy” rating to a “hold” rating in a research note on Tuesday, January 6th. Weiss Ratings upgraded Arlo Technologies from a “sell (d+)” rating to a “hold (c-)” rating in a research note on Friday, March 6th. Three analysts have rated the stock with a Buy rating and two have assigned a Hold rating to the stock. According to data from MarketBeat, Arlo Technologies presently has a consensus rating of “Moderate Buy” and a consensus target price of $23.33.

Get Our Latest Research Report on ARLO

Arlo Technologies Company Profile (Get Free Report)

Arlo Technologies, Inc (NYSE: ARLO) is a provider of smart home security products and services designed for residential and small business customers. The company offers a portfolio of wireless and Wi-Fi-enabled security cameras, video doorbells, smart lighting solutions, and associated accessories. Arlo integrates advanced video analytics, motion detection, cloud storage, and two-way audio capabilities to deliver end-to-end security and monitoring solutions accessible through mobile applications and web interfaces.

Founded as a division of Netgear, Inc in 2014 and spun off as an independent public company in 2018, Arlo Technologies has established a presence in North America, Europe, Australia and parts of Asia.

Featured Articles Five stocks we like better than Arlo Technologies

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2026-06-12 11:46 1mo ago
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A Look at Arlo Technologies Inc (ARLO) After 4.6% Gain -- GF Value $10.40 vs Price $13.72
ARLO Arlo
FMP Stock News
Original source text
On April 13, 2026, Arlo Technologies Inc ARLO shares rose 4.6% to a current price of $13.72. Over the past 52 weeks, the stock has traded between $8.50 and $19.94, showcasing significant volatility. The recent price increase comes amidst a backdrop of fluctuations, as the stock has experienced a -1.1% decline over the past week and is down 1.9% year-to-date, yet boasts a remarkable 54.5% gain over the past year.

GF Value™ verdict: Current price of $13.72 vs GF Value of $10.40 indicates the stock is 31.9% overvalued.GF Score™ of 67/100 signifies an above-average ranking in terms of overall quality and performance.Notable signal: Insider activity shows that insiders sold $9.4M worth of shares in the last three months, indicating potential caution among company leaders. Is ARLO Overvalued or Undervalued? Analyzing the discrepancy between the current price of $13.72 and the GF Value™ of $10.40 reveals that Arlo Technologies Inc is currently overvalued by approximately 31.9%. The GF Valuation label classifies the stock as significantly overvalued, suggesting caution for potential investors. A significant risk is present, as buying shares at this inflated price could expose investors to a downturn if the market corrects to reflect its intrinsic value. GF Value™ is GuruFocus' proprietary measure of intrinsic value, calculated from historical trading multiples, past business growth, and future performance estimates.

The margin of safety appears limited as the stock trades well above its calculated fair value, indicating that current investors may be paying a premium that does not align with the company's fundamentals. This valuation discrepancy may lead to a re-evaluation of the stock price if future performance does not meet market expectations.

How Does ARLO's Valuation Compare to Its History? Metric Current Historical P/E (TTM) 105.5x 115.5x (5-Year Median) Forward P/E 17.0x N/A The current P/E (TTM) of 105.5x is 9% below its 5-year median of 115.5x, indicating that the stock is trading slightly below its historical valuation multiples. However, this analysis generally aligns with the GF Value™ verdict of being overvalued, as such high P/E ratios may not be sustainable in the long run, particularly in light of the significant gap between the current price and GF Value™.

What Does ARLO's GF Score™ Tell Us? Metric Rating GF Score™ 67/100 Financial Strength 7/10 Profitability 3/10 Growth 2/10 Valuation 5/10 Momentum 8/10 The GF Score™ of 67/100 highlights that Arlo Technologies Inc holds some strong attributes, particularly in Financial Strength with a rating of 7/10 and Momentum with a rating of 8/10. However, the weaker areas, such as Profitability (3/10) and Growth (2/10), suggest that while the company may be stable, it may struggle with generating consistent profits and expanding effectively. This mixed score indicates a need for cautious evaluation before making any investment decisions.

What Are Insiders Doing with ARLO Stock? Recent insider activity shows that insiders have sold approximately $9.4 million worth of shares over the last three months, with no reported purchases. This trend can often signal a lack of confidence in the company's short-term prospects or a desire to capitalize on current stock prices. Such selling activity may raise concerns for potential investors regarding the company's future performance and strategic direction.

What This Means for Investors Based on the GF Value™ assessment, Arlo Technologies Inc ARLO is currently overvalued at a price of $13.72 in comparison to the GF Value™ of $10.40. This overvaluation suggests potential risks for investors, particularly in light of the company's recent insider selling and mixed financial metrics. Caution is advised when considering an investment in this stock.

For the complete analysis, visit the Arlo Technologies Inc ARLO stock page. You can also explore the GF Value™ page for detailed valuation methodology, or use the GuruFocus Stock Screener to find similar opportunities.

Frequently Asked Questions What is ARLO's GF Score™?

ARLO's GF Score™ is 67/100, indicating an above-average ranking in overall quality and performance, suggesting that while there are strengths, there are also significant areas for improvement.

Is ARLO overvalued or undervalued?

ARLO is currently overvalued with a GF Value™ of $10.40 compared to its current price of $13.72, indicating a potential risk for investors.

What is ARLO's P/E ratio?

ARLO's P/E ratio (TTM) is 105.5x, which is slightly below its 5-year median of 115.5x, suggesting a valuation that, while high, is marginally more favorable than historical averages.

This stock alert was generated using automated technology and GuruFocus financial data to provide readers with timely and accurate market reporting. This content was reviewed by GuruFocus editorial team prior to publication. Please send any questions or comments about this story to [email protected].