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2026-07-23 12:52 3d ago
2026-07-23 07:00 3d ago
Beam Therapeutics to Present Updated Data from Phase 1/2 Trial of BEAM-302 in Alpha-1 Antitrypsin Deficiency (AATD) in Late-Breaking Oral Presentation at the European Respiratory Society (ERS) Congress 2026
BEAM Beam Therapeutics
FMP Stock News
Original source text
CAMBRIDGE, Mass., July 23, 2026 (GLOBE NEWSWIRE) -- Beam Therapeutics Inc. (Nasdaq: BEAM), a biotechnology company developing precision genetic medicines through base editing, today announced that the company will present updated clinical data from the Phase 1/2 trial evaluating BEAM-302 for alpha-1 antitrypsin deficiency (AATD) at the European Respiratory Society (ERS) Congress 2026, taking place September 5–9, 2026, in Barcelona, Spain.
2026-07-23 08:03 3d ago
2026-07-23 02:15 3d ago
Beam Therapeutics Inc. (NASDAQ:BEAM) Given Average Rating of “Moderate Buy” by Brokerages
BEAM Beam Therapeutics
FMP Stock News
Original source text
Posted by Defense World Staff on Jul 23rd, 2026

Beam Therapeutics Inc. (NASDAQ:BEAM – Get Free Report) has received an average recommendation of “Moderate Buy” from the fourteen ratings firms that are presently covering the company, MarketBeat reports. One analyst has rated the stock with a sell rating, three have assigned a hold rating and ten have assigned a buy rating to the company. The average twelve-month target price among brokerages that have issued a report on the stock in the last year is $46.8462.

Several research firms have weighed in on BEAM. Tudor Pickering set a $39.00 target price on shares of Beam Therapeutics in a report on Wednesday, May 13th. HC Wainwright reaffirmed a “buy” rating and issued a $80.00 price target on shares of Beam Therapeutics in a report on Tuesday, July 7th. Sanford C. Bernstein lowered their price target on shares of Beam Therapeutics from $40.00 to $39.00 and set an “outperform” rating on the stock in a research report on Wednesday, May 13th. Citigroup raised their price objective on shares of Beam Therapeutics from $64.00 to $68.00 and gave the stock a “buy” rating in a research note on Thursday, March 26th. Finally, Weiss Ratings restated a “sell (d-)” rating on shares of Beam Therapeutics in a research report on Friday, July 17th.

View Our Latest Report on Beam Therapeutics

Beam Therapeutics Stock Down 2.4% Beam Therapeutics stock opened at $26.64 on Thursday. Beam Therapeutics has a fifty-two week low of $15.60 and a fifty-two week high of $38.26. The firm has a market capitalization of $2.74 billion, a price-to-earnings ratio of -39.18 and a beta of 2.18. The stock’s fifty day moving average is $31.28 and its two-hundred day moving average is $29.30. The company has a debt-to-equity ratio of 0.09, a quick ratio of 16.99 and a current ratio of 16.99.

Beam Therapeutics (NASDAQ:BEAM – Get Free Report) last released its quarterly earnings results on Thursday, May 7th. The company reported ($0.91) earnings per share (EPS) for the quarter, topping the consensus estimate of ($1.03) by $0.12. Beam Therapeutics had a negative return on equity of 29.00% and a negative net margin of 39.66%.The business had revenue of $31.74 million during the quarter, compared to the consensus estimate of $10.98 million. During the same quarter in the previous year, the company posted ($1.23) EPS. The business’s revenue was up 323.2% on a year-over-year basis. Analysts predict that Beam Therapeutics will post -4.16 EPS for the current fiscal year.

Insider Buying and Selling In other Beam Therapeutics news, insider Fmr Llc sold 251,488 shares of the stock in a transaction on Friday, June 26th. The stock was sold at an average price of $35.26, for a total transaction of $8,867,466.88. Following the sale, the insider owned 854,583 shares in the company, valued at approximately $30,132,596.58. This represents a 22.74% decrease in their position. The sale was disclosed in a filing with the Securities & Exchange Commission, which can be accessed through this link. Company insiders own 3.80% of the company’s stock.

Institutional Trading of Beam Therapeutics Institutional investors and hedge funds have recently made changes to their positions in the stock. CWM LLC grew its holdings in shares of Beam Therapeutics by 15.4% during the fourth quarter. CWM LLC now owns 2,466 shares of the company’s stock worth $68,000 after buying an additional 329 shares in the last quarter. Wealth Effects LLC lifted its stake in shares of Beam Therapeutics by 4.3% during the fourth quarter. Wealth Effects LLC now owns 9,600 shares of the company’s stock valued at $266,000 after buying an additional 400 shares during the period. Franklin Resources Inc. lifted its stake in shares of Beam Therapeutics by 2.6% during the fourth quarter. Franklin Resources Inc. now owns 21,948 shares of the company’s stock valued at $608,000 after buying an additional 566 shares during the period. Van ECK Associates Corp boosted its position in Beam Therapeutics by 48.7% during the third quarter. Van ECK Associates Corp now owns 2,158 shares of the company’s stock worth $52,000 after acquiring an additional 707 shares during the last quarter. Finally, Stifel Financial Corp boosted its position in Beam Therapeutics by 7.8% during the fourth quarter. Stifel Financial Corp now owns 13,405 shares of the company’s stock worth $372,000 after acquiring an additional 965 shares during the last quarter. 99.68% of the stock is currently owned by hedge funds and other institutional investors.

About Beam Therapeutics (Get Free Report)

Beam Therapeutics, Inc (NASDAQ: BEAM) is a biotechnology company dedicated to developing precision genetic medicines through its pioneering base editing platform. Headquartered in Cambridge, Massachusetts, with additional research facilities in Philadelphia, the company focuses on engineering molecular editors capable of making precise single-nucleotide changes in DNA. By harnessing its proprietary base editing technology, Beam aims to correct or disrupt disease-causing genetic variants at their source, offering the potential for novel therapies in areas with significant unmet medical need.

Founded in 2017 as a spin-out from Harvard University and the Broad and Whitehead Institutes, Beam was co-founded by leading academic researcher David R.

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2026-07-21 10:21 5d ago
2026-07-21 03:14 5d ago
Amova Asset Management Americas Inc. Has $91.16 Million Stock Holdings in Beam Therapeutics Inc. $BEAM
BEAM Beam Therapeutics
FMP Stock News
Original source text
Posted by Defense World Staff on Jul 21st, 2026

Amova Asset Management Americas Inc. lowered its stake in Beam Therapeutics Inc. (NASDAQ:BEAM – Free Report) by 13.2% during the first quarter, according to its most recent 13F filing with the Securities and Exchange Commission. The institutional investor owned 3,825,585 shares of the company’s stock after selling 583,715 shares during the quarter. Beam Therapeutics makes up 1.3% of Amova Asset Management Americas Inc.’s investment portfolio, making the stock its 24th largest holding. Amova Asset Management Americas Inc. owned about 3.72% of Beam Therapeutics worth $91,164,000 as of its most recent filing with the Securities and Exchange Commission.

Several other institutional investors and hedge funds have also recently bought and sold shares of BEAM. Hollencrest Capital Management purchased a new stake in shares of Beam Therapeutics in the 1st quarter valued at approximately $43,000. Bank Julius Baer & Co. Ltd Zurich acquired a new position in Beam Therapeutics in the 4th quarter worth approximately $47,000. Larson Financial Group LLC grew its position in Beam Therapeutics by 4,370.5% during the 3rd quarter. Larson Financial Group LLC now owns 1,967 shares of the company’s stock worth $48,000 after purchasing an additional 1,923 shares in the last quarter. Van ECK Associates Corp grew its position in Beam Therapeutics by 48.7% during the 3rd quarter. Van ECK Associates Corp now owns 2,158 shares of the company’s stock worth $52,000 after purchasing an additional 707 shares in the last quarter. Finally, Kestra Advisory Services LLC acquired a new stake in Beam Therapeutics during the 4th quarter valued at $59,000. Institutional investors and hedge funds own 99.68% of the company’s stock.

Insider Buying and Selling In other news, insider Fmr Llc sold 251,488 shares of the stock in a transaction on Friday, June 26th. The shares were sold at an average price of $35.26, for a total transaction of $8,867,466.88. Following the transaction, the insider owned 854,583 shares in the company, valued at $30,132,596.58. This represents a 22.74% decrease in their position. The sale was disclosed in a document filed with the SEC, which can be accessed through this hyperlink. 3.80% of the stock is owned by corporate insiders.

Beam Therapeutics Stock Down 4.4% BEAM opened at $26.33 on Tuesday. Beam Therapeutics Inc. has a fifty-two week low of $15.60 and a fifty-two week high of $38.26. The business has a 50-day moving average of $31.47 and a 200-day moving average of $29.31. The company has a debt-to-equity ratio of 0.09, a current ratio of 16.99 and a quick ratio of 16.99. The company has a market capitalization of $2.71 billion, a PE ratio of -38.72 and a beta of 2.18.

Beam Therapeutics (NASDAQ:BEAM – Get Free Report) last announced its quarterly earnings results on Thursday, May 7th. The company reported ($0.91) EPS for the quarter, beating the consensus estimate of ($1.03) by $0.12. The business had revenue of $31.74 million during the quarter, compared to analysts’ expectations of $10.98 million. Beam Therapeutics had a negative return on equity of 29.00% and a negative net margin of 39.66%.The firm’s quarterly revenue was up 323.2% compared to the same quarter last year. During the same quarter in the previous year, the business posted ($1.23) EPS. Equities research analysts forecast that Beam Therapeutics Inc. will post -4.16 EPS for the current fiscal year.

Wall Street Analysts Forecast Growth Several analysts have recently commented on BEAM shares. Citigroup raised their target price on Beam Therapeutics from $64.00 to $68.00 and gave the stock a “buy” rating in a research report on Thursday, March 26th. Sanford C. Bernstein dropped their price target on Beam Therapeutics from $40.00 to $39.00 and set an “outperform” rating on the stock in a research report on Wednesday, May 13th. HC Wainwright reissued a “buy” rating and issued a $80.00 price objective on shares of Beam Therapeutics in a research note on Tuesday, July 7th. Bank of America restated a “buy” rating and set a $47.00 price objective on shares of Beam Therapeutics in a research report on Wednesday, July 8th. Finally, Tudor Pickering set a $39.00 target price on Beam Therapeutics in a report on Wednesday, May 13th. Ten research analysts have rated the stock with a Buy rating, three have assigned a Hold rating and one has given a Sell rating to the company. According to MarketBeat, the stock currently has a consensus rating of “Moderate Buy” and an average price target of $46.85.

View Our Latest Research Report on BEAM

About Beam Therapeutics (Free Report)

Beam Therapeutics, Inc (NASDAQ: BEAM) is a biotechnology company dedicated to developing precision genetic medicines through its pioneering base editing platform. Headquartered in Cambridge, Massachusetts, with additional research facilities in Philadelphia, the company focuses on engineering molecular editors capable of making precise single-nucleotide changes in DNA. By harnessing its proprietary base editing technology, Beam aims to correct or disrupt disease-causing genetic variants at their source, offering the potential for novel therapies in areas with significant unmet medical need.

Founded in 2017 as a spin-out from Harvard University and the Broad and Whitehead Institutes, Beam was co-founded by leading academic researcher David R.

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2026-07-20 19:57 5d ago
2026-07-20 13:30 6d ago
Cathie Wood Is Buying This Up-and-Coming Biotech Stock. Should You Follow Her Lead?
BEAM Beam Therapeutics
FMP Stock News
Original source text
Cathie Wood of Ark Invest first bought shares of Beam Therapeutics (BEAM 4.36%), a biotech focused on precision genetic treatments, in 2020. She's continued to acquire shares since then, with her most recent purchases last week clocking in at around $4 million.

Today, Wood's position in Beam is worth more than $300 million. That's not trivial, even for Wood. Of course, the question is: When it comes to Beam, should you follow her lead? I maintain that if you're comfortable with the risks of an early-stage biotech company, you should.

Beam is taking a different approach to gene editing CRISPR gene editing involves cutting both strands of DNA before inserting or removing genetic material. Beam Therapeutics, however, uses a different technology called base editing.

Instead of cutting DNA, base editing changes a single DNA letter directly. Think of it as correcting a typo in a document rather than deleting an entire sentence and rewriting it. The approach is designed to make genetic edits more precise.

Image source: Getty Images.

That technology becomes quite attractive when you consider that among more than 50,000 documented disease-causing genetic variants, roughly 60% are point mutations (a genetic alteration in which a single nucleotide in a DNA or RNA sequence is changed), making them potential targets for base editing.

A maturing pipeline Beam now has several clinical programs that could create significant value over the next few years. Its most advanced liver-disease program, BEAM-302, is being developed for alpha-1 antitrypsin deficiency (an inherited disorder that leaves the liver and lungs vulnerable to progressive damage).

Updated phase 1/2 data showed that a single treatment produced substantial increases in functional alpha-1 antitrypsin protein. The company has selected its optimal dose and expects to begin a global clinical trial in the second half of 2026.

Beam is also developing ristoglogene autogetemcel (risto-cel), a potential one-time treatment for sickle cell disease. So far, clinical results have been encouraging, showing that the therapy can restore healthy function to red blood cells by increasing production of fetal hemoglobin. This is a key protein that helps prevent the painful complications caused by the disease.

The company expects to file for approval from the U.S. Food and Drug Administration (FDA) by the end of 2026. If approved, risto-cel would become Beam's first commercial product, transforming it from a company focused solely on research into one capable of generating product revenue.

Beam also plans to seek FDA approval to begin human testing of BEAM-304, a potential treatment for phenylketonuria (PKU). This rare inherited disorder prevents the body from properly breaking down the amino acid phenylalanine. Left untreated, the condition can lead to serious neurological problems.

The company will also soon report its first clinical results for BEAM-301, a treatment for glycogen storage disease type Ia, a rare genetic disorder that prevents the liver from properly regulating blood sugar. While both programs are still in the early stages, they broaden Beam's pipeline and provide additional opportunities to create long-term value if the therapies prove successful.

Plenty of cash One of the biggest risks for early-stage biotech companies is running out of cash before reaching meaningful clinical milestones. Beam appears to be in a stronger position than many of its peers.

At the end of the first quarter, the company reported $1.21 billion in cash, cash equivalents, and marketable securities. Management believes that its cash, combined with a financing deal it has with specialty finance firm Sixth Street, is sufficient to fund operations through mid-2029. That gives Beam time to advance multiple clinical programs without immediately returning to capital markets for additional financing.

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Of course, none of this guarantees success. Beam Therapeutics reported a net loss of $94.3 million in Q1. Every major value driver still depends on successful clinical trials, regulatory approvals, and eventual commercialization. Failure in even one late-stage program could significantly affect the stock.

Competition also continues to intensify. Companies including CRISPR Therapeutics and Verve Therapeutics (now a subsidiary of Eli Lilly) continue advancing their own gene-editing platforms. Beam's long-term success depends not only on proving that base editing works, but also that it offers meaningful advantages over competing technologies.

Wood typically invests in companies capable of creating entirely new markets rather than simply improving existing ones. Beam fits that profile. The company has a differentiated gene-editing platform, multiple late-stage clinical catalysts over the next 18 months, more than $1.2 billion on its balance sheet, and enough capital to execute its development strategy well into 2029.

That doesn't make Beam a low-risk investment. Clinical-stage biotechnology rarely is. But if you're willing to accept the volatility that comes with drug development, Beam Therapeutics appears to be one of the more compelling gene-editing companies on the market today.
2026-07-09 15:09 17d ago
2026-07-09 10:22 17d ago
Prime Medicine Beats Beam Therapeutics In Patent Dispute - But Both Are Investable
BEAM Beam Therapeutics
FMP Stock News
Original source text
Prime Medicine, Inc. secured a favorable arbitration ruling against Beam Therapeutics, allowing continued development of its PM647 gene editing program for AATD. PRME's Prime Editing platform offers precise, versatile gene correction using LNP delivery, but remains preclinical with IND/CTA filings for PM647 expected mid-2026 and initial clinical data in 2027. PRME lags competitors like Beam, Sanofi, and Arrowhead in the AATD development race, facing significant funding needs and clinical risks.
2026-07-08 19:58 17d ago
2026-07-08 13:29 18d ago
Prime Medicine Secures Favorable Arbitration Ruling in Beam Therapeutics Case
BEAM Beam Therapeutics
FMP Stock News
Original source text
The tribunal on Wednesday determined that Prime Medicine’s investigational gene-editing therapy PM647 falls within the scope of the companies’ 2019 Collaboration and License Agreement.

The decision clears the company of any breach of contract claims and eliminates any financial liability related to the case.

Tribunal Rules PM647 Falls Within Prime Medicine’s Licensed FieldAccording to Prime Medicine, the arbitration tribunal concluded that PM647 is covered under the company’s defined “Field” in the 2019 agreement with Beam Therapeutics.

As a result, the tribunal found that Prime Medicine did not violate the terms of the agreement.

The company added that the ruling also determined it owes no monetary damages to Beam Therapeutics, bringing the previously disclosed arbitration to a close.

PM647 Targets Most Common Cause of Alpha-1 Antitrypsin DeficiencyPM647 is Prime Medicine’s investigational Prime Editing therapy for Alpha-1 Antitrypsin Deficiency (AATD).

The therapy uses the company’s universal liver lipid nanoparticle (LNP) delivery platform to correct the E342K (Pi*Z) mutation in the SERPINA1 gene, which the company said is the most common disease-causing mutation associated with AATD.

Prime Medicine said that in fully humanized mouse models, PM647 achieved high editing efficiency while restoring the corrected M-AAT protein isoform to healthy human levels at clinically relevant doses.

Clinical Development Timeline Remains On TrackFollowing the arbitration outcome, Prime Medicine said it remains on schedule to advance PM647 into the clinic.

The company plans to submit an investigational new drug application and/or a clinical trial application for PM647 during the third quarter of 2026.

If those filings proceed as planned, Prime Medicine expects to report initial clinical data from the program in 2027.

PRME Price Action: Prime Medicine shares were up 13.16% at $4.51 at the time of publication on Wednesday, according to Benzinga Pro data.

Photo by Gorodenkoff via Shutterstock

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2026-07-08 10:23 18d ago
2026-07-08 05:45 18d ago
A New CRISPR "DNA Shredder" Could Change Gene-Editing -- What It Means for CRISPR Therapeutics
BEAM Beam Therapeutics
FMP Stock News
Original source text
An exciting new CRISPR-based tool is making waves in the scientific literature this spring. Because the new technology destroys targeted diseased cells outright rather than editing their genetic material, it's being informally called the "DNA shredder."

For shareholders of CRISPR Therapeutics (CRSP 1.81%) and its gene-editing peers like Intellia Therapeutics (NTLA 2.30%) and Beam Therapeutics (BEAM +7.36%), the emergence of a new form of genetic medicine could have major financial implications down the road. Let's unpack what the new tech can do and what it means for CRISPR Therapeutics as well as these other stocks.

Image source: Getty Images.

This is the frontier of science, not a near-term commercial event The newly discovered tool reads a signal unique to a diseased cell and subsequently destroys that cell's DNA by cutting it into fragments faster than the cell can repair it. That continues until the cell dies once it can't reproduce its own cellular machinery; cells without the triggering sequence are spared.

In short, this is programmable cell-killing and not gene-editing. And that's a capability that could be enormously useful across a range of clinical and research applications.

The new tool is already demonstrating its potential to treat serious illnesses. A May paper published in the journal Nature from researchers at the University of Utah showed the therapy cutting the growth of lung cancer cells that are driven by mutations in one of the most common cancer-driving genes by about 50% in a lab dish. That matched the chemotherapy drug cisplatin in the same test, with no effect on healthy cells.

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A follow-up Nature paper in June from a lab at University of California, Berkeley -- one of the two labs whose 2012 work established CRISPR-Cas9 as a programmable gene-editing tool -- extended the shredding approach to target a gene that's mutated in 40% to 50% of all cancers, and one of oncology's most challenging targets to develop drugs for. All of this work remains in test tubes and animal models, with the obstacle of developing the shredder technology into a medicine that's useful to treat human patients still unsolved.

None of this new tech is in CRISPR Therapeutics' pipeline, nor in the disclosed pipelines of any of its major competitors. The closest it gets is using this editing to produce Casgevy, which CRISPR Therapeutics developed with Vertex Pharmaceuticals. Similarly, Intellia Therapeutics uses this editing as part of its candidates to treat hereditary angioedema (severe swelling) and transthyretin amyloidosis (a progressive, life-threatening disease caused by a buildup of abnormal protein deposits in organs and tissues). Beam Therapeutics uses base editors in alpha-1 antitrypsin deficiency and sickle cell disease.

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The only company working to develop a therapy using the tool is Akribion Therapeutics, a private German biotech. Its lead program targets HPV-positive head and neck cancer, but it's years from clinical trials, let alone the market.

What investors should actually take from this The most important takeaway for investors here is that the new papers significantly expand the addressable market for CRISPR-based medicine.

The ability to perform efficient cell destruction based on a genetic sequence addresses a huge problem that gene-editing alone doesn't address, specifically the possibility of competing in areas like oncology and virally driven cancers, where killing the diseased cells could constitute a breakthrough in treatment. None of the public CRISPR names is anywhere near such a breakthrough with this today, and it's unclear if they even have enough capital or expertise in oncology to pursue new programs using the shredder technology.

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But there is one vector where CRISPR Therapeutics and the other gene-editing stocks could become relevant players. The paper in the May issue of Nature showed promise in the same drug-delivery infrastructure that CRISPR Therapeutics, Intellia, and Beam have spent a half-decade building for their particular purposes. Having a functional delivery system for a gene-editing complex means that the next payload they invent doesn't need to include spending on making new delivery infrastructure.

So the incumbents will likely have an advantage relative to newcomers if they choose to compete.
2026-06-20 17:12 1mo ago
2026-06-18 07:00 1mo ago
Beam Therapeutics Announces Clearance of Investigational New Drug Application for BEAM-304 for the Treatment of Phenylketonuria (PKU) by the United States (U.S.) Food and Drug Administration
BEAM Beam Therapeutics
FMP Stock News
Original source text
June 18, 2026 07:00 ET  | Source: Beam Therapeutics

BEAM-304 Development Approach Has Potential to Create Transformative, One-time Therapies for the Majority of Patients with PKU 

BEAM-304 Program Designed as Platform-based Approach Reflecting Emerging FDA Guidance for Accelerated Development of Genome Editing Therapies

New Preclinical Data for BEAM-304 to be Presented at FASEB Genome Engineering: Research and Applications Conference

CAMBRIDGE, Mass., June 18, 2026 (GLOBE NEWSWIRE) -- Beam Therapeutics Inc. (Nasdaq: BEAM), a biotechnology company developing precision genetic medicines through base editing, today announced that the United States (U.S.) Food and Drug Administration (FDA) has cleared the investigational new drug (IND) application for BEAM-304 for the treatment of phenylketonuria (PKU). PKU is a rare, inherited metabolic disorder that results in toxic accumulation of phenylalanine (Phe), leading to serious neurologic and neurocognitive impairments and requires strict, lifelong dietary management. Beam is advancing BEAM-304 using an innovative development approach in which multiple mutation-specific base editors are developed efficiently within a single clinical program using in vivo delivery, in accordance with the FDA’s recent efforts to accelerate development of genome editing therapies.1

“PKU affects approximately 20,000 people in the U.S., with significant unmet need for therapies that address the underlying cause of disease,” said Giuseppe Ciaramella, Ph.D., president of Beam. “FDA clearance of our IND for BEAM-304 supports our novel approach of developing multiple mutation-specific base editors through a single clinical platform program, leveraging emerging FDA guidance intended to accelerate development of base editing therapeutics. We look forward to initiating our Phase 1/2 trial, intending to establish clinical proof of concept for base editing in PKU.”

“Many PKU-causing mutations are single-base changes, making the disease particularly well suited for correction through base editing,” said Gopi Shanker, Ph.D., chief scientific officer of Beam. “By leveraging the same underlying base editing technology, LNP delivery system, and manufacturing approach across multiple mutation-specific editors, we believe we can establish a scalable development pathway that expands access to potentially transformative therapies for people living with PKU and may serve as a model for addressing other genetically diverse liver diseases in the future.”

BEAM-304 leverages Beam’s proprietary and clinically validated base editing technology and lipid nanoparticle (LNP) delivery capabilities to directly and durably correct mutations in the phenylalanine hydroxylase (PAH) gene that cause PKU. By correcting mutations in the PAH gene, BEAM-304 aims to restore PAH enzyme activity in order to reduce toxic Phe to the recommended guideline levels (≤ 360 µmol/L) while enabling diet normalization and freedom from medical food.

Preclinical data demonstrate that BEAM-304 normalized plasma Phe levels in PKU mouse models at clinically relevant doses with robust on-target editing in the liver. Updated preclinical data for BEAM-304 will be presented at the Federation of American Societies for Experimental Biology (FASEB) Genome Engineering: Research and Applications Conference, taking place July 6-9, 2026, in Porto, Portugal.

The planned Phase 1/2 trial will initially evaluate safety, tolerability, reduction of blood Phe levels and diet liberalization in PKU patients with the R408W mutation, followed by a base editor designed to address a second mutation, with the goal of establishing clinical proof of concept for base editing in PKU.

About BEAM-304
BEAM-304 is a liver-targeting lipid-nanoparticle (LNP) formulation of base editing reagents designed to correct mutations in the phenylalanine hydroxylase (PAH) gene that cause phenylketonuria (PKU). By correcting mutations in the PAH gene, BEAM-304 aims to reduce toxic Phe to within recommended guidelines while enabling normalization of diet and freedom from medical food. BEAM-304 is delivered via an intravenous infusion. BEAM-304 will be evaluated in a Phase 1/2, open-label, dose exploration and dose expansion clinical trial to investigate its safety, tolerability, pharmacodynamics, pharmacokinetics and efficacy in PKU patients. Beam is advancing BEAM-304 using an innovative development approach in which multiple mutation-specific base editors are developed efficiently within a single clinical program. Initial clinical development will focus on base editors addressing the two most prevalent variants found in nearly half of patients with PKU in the U.S., with ongoing research efforts to address additional pathogenic mutations.

About Phenylketonuria (PKU)
Phenylketonuria (PKU) is a rare, inherited metabolic disorder caused by pathogenic variants in the phenylalanine hydroxylase (PAH) gene, resulting in the inability to properly metabolize phenylalanine (Phe), an essential amino acid. Elevated blood Phe levels can lead to serious and irreversible brain damage and neurological complications, including cognitive impairment, developmental delays, and psychiatric symptoms, if not adequately controlled. PKU affects approximately 20,000 individuals in the United States and is typically diagnosed in infancy through newborn screening. There are no currently approved curative treatments for PKU. Current treatment options often require lifelong dietary restriction and chronic disease management, and many patients continue to experience significant unmet medical need.

About Beam Therapeutics
Beam Therapeutics (Nasdaq: BEAM) is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Beam’s suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of potential therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing lifelong cures to patients suffering from serious diseases.

Cautionary Note Regarding Forward-Looking Statements
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Investors are cautioned not to place undue reliance on these forward-looking statements, including, but not limited to, statements related to: the therapeutic applications and potential of our technology, including with respect to PKU; our plans, and anticipated timing, to advance our PKU program; the clinical trial designs and expectations for BEAM-304; our expected presentation at the FASEB conference; our anticipated regulatory interactions and filings; and our ability to develop lifelong, curative, precision genetic medicines for patients through base editing. Each forward-looking statement is subject to important risks and uncertainties that could cause actual results to differ materially from those expressed or implied in such statement, including, without limitation, risks and uncertainties related to: our ability to develop, obtain regulatory approval for, and commercialize our product candidates, which may take longer or cost more than planned; our ability to raise additional funding, which may not be available; our ability to obtain, maintain and enforce patent and other intellectual property protection for our product candidates; the uncertainty that our product candidates will receive regulatory approval necessary to initiate or continue human clinical trials; that preclinical testing of our product candidates and preliminary or interim data from preclinical studies and clinical trials may not be predictive of the results or success of ongoing or later clinical trials; that initiation and enrollment of, and anticipated timing to advance, our clinical trials may take longer than expected; that our product candidates, including the delivery modalities we rely on to administer them, may cause serious adverse events; that our product candidates may experience manufacturing or supply interruptions or failures; risks related to competitive products; and the other risks and uncertainties identified under the headings “Risk Factors Summary” and “Risk Factors” in our Annual Report on Form 10-K for the year ended December 31, 2025, our Quarterly Report on Form 10-Q for the quarter ended March 31, 2026, and in any subsequent filings with the Securities and Exchange Commission. These forward-looking statements speak only as of the date of this press release. Factors or events that could cause our actual results to differ may emerge from time to time, and it is not possible for us to predict all of them. We undertake no obligation to update any forward-looking statement, whether as a result of new information, future developments or otherwise, except as may be required by applicable law.

Contacts:

Investors:
Holly Manning
Beam Therapeutics
[email protected]

Media:
Josie Butler
1AB
[email protected]

________________________________
1 U.S. Food and Drug Administration. FDA Issues Draft Guidance to Help Accelerate Cell and Gene Therapies for Patients. Press release. June 2, 2026. Available at: https://www.fda.gov/news-events/press-announcements/fda-issues-draft-guidance-help-accelerate-cell-and-gene-therapies-patients. Accessed June 11, 2026.
2026-06-20 17:12 1mo ago
2026-06-19 11:36 1mo ago
BEAM Stock Gains 5% as FDA Clears BEAM-304 IND for Phenylketonuria
BEAM Beam Therapeutics
FMP Stock News
Original source text
Key Takeaways BEAM shares rose 5% after the FDA cleared the IND for BEAM-304, a gene-editing therapy for PKU.BEAM-304 targets PAH gene mutations to lower toxic Phe levels and restore PAH function.BEAM plans to initiate a phase I/II study & later expand the program to target a second mutation. Shares of Beam Therapeutics (BEAM - Free Report) rose 5% on Thursday after the FDA cleared the investigational new drug (IND) application for BEAM-304, the company’s investigational gene-editing therapy for the treatment of phenylketonuria (PKU). The clearance marks an important milestone for Beam Therapeutics as it expands its liver-targeted genetic disease franchise.

PKU is a rare inherited metabolic disorder characterized by the inability to properly break down phenylalanine (Phe), resulting in its toxic buildup in the body. If left untreated, elevated Phe levels can lead to serious neurological and cognitive complications, requiring patients to adhere to strict lifelong dietary restrictions.The disease affects approximately 20,000 people in the United States and is typically diagnosed through newborn screening. Currently, no approved curative treatments exist for PKU.

Year to date, the stock has risen 23.2% against the industry’s 1% decline.

Image Source: Zacks Investment Research

More on Beam Therapeutics’ BEAM-304BEAM-304 is a liver-targeted, lipid nanoparticle (LNP)-based gene-editing therapy designed to correct disease-causing mutations in the phenylalanine hydroxylase (PAH) gene responsible for PKU. By restoring PAH function, the therapy aims to lower toxic Phe levels, potentially allowing patients to maintain a normal diet without relying on specialized medical foods.

The candidate is being developed using an innovative approach that enables efficient evaluation of multiple mutation-specific base editors within a single clinical program through in vivo delivery. This strategy aligns with the FDA’s efforts to accelerate the development of genome-editing treatments for serious genetic diseases.

In preclinical studies, BEAM-304 demonstrated robust on-target liver editing and normalization of Phe levels in PKU mouse models at clinically relevant doses, supporting its potential as a disease-modifying therapy.

Beam plans to evaluate BEAM-304 in a phase I/II open-label clinical study designed to initially assess the safety, tolerability, blood Phe reduction and the potential for dietary liberalization of BEAM-304 in PKU patients with the R408W mutation. The therapy will be administered as an intravenous infusion. The program will then expand to evaluate a base editor targeting a second mutation, with the aim of establishing clinical proof of concept for base editing in PKU.

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

Some better-ranked stocks in the biotech sector are Indivior Pharmaceuticals (INDV - Free Report) , Liquidia Corporation (LQDA - Free Report) and Immunocore (IMCR - Free Report) , each 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 30 days, earnings per share estimates for Indivior Pharmaceuticals remained unchanged at $4.05 for 2026 and $4.27 for 2027. INDV shares have risen 6.7% year to date.

Indivior Pharmaceuticals’ earnings beat estimates in each of the trailing four quarters, with the average surprise being 65.44%.

Over the past 30 days, estimates for Liquidia’s earnings per share remained unchanged at $2.97 for 2026 and $4.81 for 2027. LQDA shares have surged 106.1% year to date.

Liquidia’s earnings beat estimates in three of the trailing four quarters and missed in the remaining one, with the average surprise being 54.40%.

Over the past 30 days, earnings per share estimates for Immunocore’s 2026 were unchanged at 6 cents for 2026 and 87 cents for 2027. IMCR shares have lost 17.6% year to date.

Immunocore’s earnings beat estimates in three of the trailing four quarters and missed in the remaining one, the average surprise being 46.66%.
2026-06-17 06:53 1mo ago
2026-06-16 09:51 1mo ago
Beam Therapeutics Stock Soars 21% in Three Months: Here's Why
BEAM Beam Therapeutics
FMP Stock News
Original source text
Key Takeaways BEAM stock rose 21% over the past three months, driven by positive BEAM-302 phase I/II data in AATD.BEAM plans an accelerated approval path for BEAM-302 and expects to initiate a global cohort in H2 2026.BEAM ended Q1 2026 with about $1.2B in cash. Funding is expected to support operations into mid-2029. Shares of Beam Therapeutics (BEAM - Free Report) have risen 21% over the past three months against the industry’s 4.5% decline, primarily driven by positive clinical developments. Investor sentiment has also been bolstered by rapid regulatory progress across the company’s pipeline, strengthening confidence in its base-editing platform and in its strong financial position.

Image Source: Zacks Investment Research

Strong Clinical Data From BEAM-302An important catalyst behind the stock’s rally has been the encouraging early data announced in late March from an ongoing phase I/II dose-escalation study evaluating its pipeline candidate, BEAM-302, for the treatment of patients with alpha-1 antitrypsin deficiency (AATD), across multiple dose levels. BEAM-302 is a liver-targeting lipid-nanoparticle formulation of base editing reagents designed to correct the disease-causing PiZ mutation.

The study demonstrated that BEAM-302 produced durable increases in functional AAT levels, significant reductions in mutant Z-AAT and the generation of corrected M-AAT, with a favorable safety profile across single doses up to 75 mg.

BEAM plans to advance BEAM-302 via an accelerated approval pathway, based on a primary endpoint of AAT biomarkers evaluated for more than 12 months, with the 60 mg selected as the optimal biological dose for further development.

To support a future biologics license application (BLA), the company anticipates enrolling approximately 50 additional patients with AATD-related lung disease, with or without liver involvement, by expanding its ongoing open-label phase I/II study. BEAM expects to initiate the global cohort in the second half of 2026.

Multiple Upcoming Pipeline CatalystsBeyond BEAM-302, investors have become increasingly optimistic about BEAM's broader pipeline. The company remains on track to submit a BLA for risto-cel, its investigational sickle cell disease therapy, by the end of 2026.

Beam Therapeutics is also expanding its genetic disease pipeline by developing BEAM-301 for the treatment of glycogen storage disease type 1a in a phase I/II dose-exploration study. Initial data from the study are expected in 2026.

The company expanded its liver-targeted genetic disease franchise with BEAM-304 for the treatment of phenylketonuria and plans to file an investigational new drug application with the FDA in 2026.

Dosing in the ongoing phase I healthy volunteer study, evaluating BEAM-103, an anti-CD117 monoclonal antibody for the treatment of SCD, is expected to be completed in 2026.

BEAM’s Strong Financial PositionBeam has historically maintained a large cash runway, which reassures investors that it can fund ongoing clinical development without near-term dilution concerns.

The company reported approximately $1.2 billion in cash, cash equivalents and marketable securities at the end of the first quarter of 2026. Management expects its cash position, including the initial $100 million received and an anticipated additional $100 million under its financing agreement with Sixth Street, to support operations into mid-2029.

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

Some better-ranked stocks in the biotech sector are Indivior Pharmaceuticals (INDV - Free Report) , Liquidia Corporation (LQDA - Free Report) and Immunocore (IMCR - Free Report) , each 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 30 days, earnings per share estimates for Indivior Pharmaceuticals remained unchanged at $4.05 for 2026 and $4.27 for 2027. INDV shares have risen 7% year to date.

Indivior Pharmaceuticals’ earnings beat estimates in each of the trailing four quarters, with the average surprise being 65.44%.

Over the past 30 days, estimates for Liquidia’s earnings per share remained unchanged at $2.97 for 2026 and $4.81 for 2027. LQDA shares have gained 108.3% year to date.

Liquidia’s earnings beat estimates in three of the trailing four quarters and missed in the remaining one, with the average surprise being 54.40%.

Over the past 30 days, earnings per share estimates for Immunocore’s 2026 were unchanged at 6 cents for 2026 and 87 cents for 2027. IMCR shares have lost 17.6% year to date.

Immunocore’s earnings beat estimates in three of the trailing four quarters and missed in the remaining one, the average surprise being 46.66%.
2026-06-12 14:36 1mo ago
2026-04-07 05:40 3mo ago
Beam Therapeutics (NASDAQ:BEAM) Insider Christine Bellon Sells 5,956 Shares
BEAM Beam Therapeutics
FMP Stock News
Original source text
Posted by Defense World Staff on Apr 7th, 2026

Beam Therapeutics Inc. (NASDAQ:BEAM – Get Free Report) insider Christine Bellon sold 5,956 shares of Beam Therapeutics stock in a transaction on Wednesday, April 1st. The stock was sold at an average price of $24.58, for a total value of $146,398.48. Following the sale, the insider owned 109,711 shares in the company, valued at $2,696,696.38. The trade was a 5.15% decrease in their ownership of the stock. The transaction was disclosed in a document filed with the Securities & Exchange Commission, which is accessible through the SEC website. The transaction was executed under a pre-arranged Rule 10b5-1 trading plan. The sale was made to cover tax withholding obligations related to the vesting of equity awards.

Christine Bellon also recently made the following trade(s):

On Thursday, January 22nd, Christine Bellon sold 1,371 shares of Beam Therapeutics stock. The stock was sold at an average price of $34.00, for a total value of $46,614.00. On Thursday, January 15th, Christine Bellon sold 18,629 shares of Beam Therapeutics stock. The stock was sold at an average price of $34.61, for a total value of $644,749.69. Beam Therapeutics Price Performance NASDAQ BEAM opened at $24.23 on Tuesday. The stock has a market capitalization of $2.47 billion, a price-to-earnings ratio of -23.99 and a beta of 2.18. Beam Therapeutics Inc. has a one year low of $13.52 and a one year high of $36.44. The business’s fifty day moving average is $26.51 and its 200-day moving average is $26.43.

Beam Therapeutics (NASDAQ:BEAM – Get Free Report) last posted its quarterly earnings results on Tuesday, February 24th. The company reported $2.33 EPS for the quarter, topping analysts’ consensus estimates of ($1.13) by $3.46. The company had revenue of $114.11 million for the quarter, compared to analysts’ expectations of $13.22 million. Beam Therapeutics had a negative net margin of 57.24% and a negative return on equity of 30.65%. Beam Therapeutics’s revenue was up 280.3% on a year-over-year basis. During the same quarter in the previous year, the firm posted ($1.09) EPS. Research analysts expect that Beam Therapeutics Inc. will post -4.57 EPS for the current fiscal year.

Institutional Investors Weigh In On Beam Therapeutics A number of hedge funds and other institutional investors have recently bought and sold shares of BEAM. Jones Financial Companies Lllp raised its holdings in Beam Therapeutics by 55,780.0% during the 1st quarter. Jones Financial Companies Lllp now owns 33,528 shares of the company’s stock valued at $655,000 after acquiring an additional 33,468 shares during the period. UBS AM A Distinct Business Unit of UBS Asset Management Americas LLC raised its holdings in Beam Therapeutics by 10.8% during the 1st quarter. UBS AM A Distinct Business Unit of UBS Asset Management Americas LLC now owns 438,529 shares of the company’s stock valued at $8,564,000 after acquiring an additional 42,609 shares during the period. Legal & General Group Plc raised its holdings in Beam Therapeutics by 8.5% during the 2nd quarter. Legal & General Group Plc now owns 102,646 shares of the company’s stock valued at $1,746,000 after acquiring an additional 8,023 shares during the period. Rhumbline Advisers raised its holdings in Beam Therapeutics by 7.2% during the 2nd quarter. Rhumbline Advisers now owns 151,372 shares of the company’s stock valued at $2,575,000 after acquiring an additional 10,168 shares during the period. Finally, Prudential Financial Inc. bought a new stake in shares of Beam Therapeutics during the second quarter valued at about $201,000. Institutional investors own 99.68% of the company’s stock.

Wall Street Analyst Weigh In A number of equities research analysts recently commented on the stock. UBS Group assumed coverage on shares of Beam Therapeutics in a report on Wednesday, January 7th. They issued a “neutral” rating and a $28.00 price target on the stock. Citigroup boosted their price objective on Beam Therapeutics from $64.00 to $68.00 and gave the company a “buy” rating in a research note on Thursday, March 26th. Sanford C. Bernstein boosted their price objective on Beam Therapeutics from $37.00 to $41.00 and gave the company an “outperform” rating in a research note on Tuesday, January 20th. Canaccord Genuity Group started coverage on Beam Therapeutics in a research note on Friday, February 20th. They issued a “buy” rating and a $74.00 price objective on the stock. Finally, Wedbush boosted their price objective on Beam Therapeutics from $57.00 to $65.00 and gave the company an “outperform” rating in a research note on Wednesday, February 25th. One analyst has rated the stock with a Strong Buy rating, eleven have assigned a Buy rating, three have issued a Hold rating and one has issued a Sell rating to the stock. Based on data from MarketBeat, the company has a consensus rating of “Moderate Buy” and an average price target of $49.36.

View Our Latest Research Report on Beam Therapeutics

Beam Therapeutics Company Profile (Get Free Report)

Beam Therapeutics, Inc (NASDAQ: BEAM) is a biotechnology company dedicated to developing precision genetic medicines through its pioneering base editing platform. Headquartered in Cambridge, Massachusetts, with additional research facilities in Philadelphia, the company focuses on engineering molecular editors capable of making precise single-nucleotide changes in DNA. By harnessing its proprietary base editing technology, Beam aims to correct or disrupt disease-causing genetic variants at their source, offering the potential for novel therapies in areas with significant unmet medical need.

Founded in 2017 as a spin-out from Harvard University and the Broad and Whitehead Institutes, Beam was co-founded by leading academic researcher David R.

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2026-06-12 14:36 1mo ago
2026-04-07 05:40 3mo ago
Beam Therapeutics (NASDAQ:BEAM) Insider Amy Simon Sells 6,700 Shares
BEAM Beam Therapeutics
FMP Stock News
Original source text
Posted by Defense World Staff on Apr 7th, 2026

Beam Therapeutics Inc. (NASDAQ:BEAM – Get Free Report) insider Amy Simon sold 6,700 shares of the business’s stock in a transaction dated Wednesday, April 1st. The shares were sold at an average price of $24.58, for a total transaction of $164,686.00. Following the transaction, the insider directly owned 102,735 shares of the company’s stock, valued at $2,525,226.30. The trade was a 6.12% decrease in their ownership of the stock. The transaction was disclosed in a document filed with the Securities & Exchange Commission, which is available through this hyperlink. The transaction was executed under a pre-arranged Rule 10b5-1 trading plan. The sale was made to cover tax withholding obligations related to the vesting of equity awards.

Beam Therapeutics Stock Down 1.7% Beam Therapeutics stock opened at $24.23 on Tuesday. The firm has a 50-day moving average price of $26.51 and a two-hundred day moving average price of $26.43. The firm has a market capitalization of $2.47 billion, a price-to-earnings ratio of -23.99 and a beta of 2.18. Beam Therapeutics Inc. has a 52-week low of $13.52 and a 52-week high of $36.44.

Beam Therapeutics (NASDAQ:BEAM – Get Free Report) last posted its earnings results on Tuesday, February 24th. The company reported $2.33 earnings per share (EPS) for the quarter, beating analysts’ consensus estimates of ($1.13) by $3.46. The firm had revenue of $114.11 million during the quarter, compared to analyst estimates of $13.22 million. Beam Therapeutics had a negative net margin of 57.24% and a negative return on equity of 30.65%. Beam Therapeutics’s revenue was up 280.3% on a year-over-year basis. During the same period in the previous year, the business posted ($1.09) EPS. Research analysts expect that Beam Therapeutics Inc. will post -4.57 earnings per share for the current year.

Institutional Trading of Beam Therapeutics Several institutional investors have recently modified their holdings of the company. Purpose Unlimited Inc. acquired a new stake in shares of Beam Therapeutics in the fourth quarter valued at $80,000. Invesco Ltd. lifted its holdings in shares of Beam Therapeutics by 20.5% in the fourth quarter. Invesco Ltd. now owns 213,185 shares of the company’s stock valued at $5,909,000 after buying an additional 36,321 shares during the period. Axxcess Wealth Management LLC acquired a new stake in shares of Beam Therapeutics in the fourth quarter valued at $212,000. XTX Topco Ltd acquired a new stake in Beam Therapeutics during the fourth quarter valued at approximately $426,000. Finally, Virtus Investment Advisers LLC lifted its stake in Beam Therapeutics by 49.0% during the fourth quarter. Virtus Investment Advisers LLC now owns 9,724 shares of the company’s stock valued at $270,000 after purchasing an additional 3,200 shares during the last quarter. Institutional investors and hedge funds own 99.68% of the company’s stock.

Analysts Set New Price Targets BEAM has been the subject of a number of analyst reports. Sanford C. Bernstein boosted their price target on Beam Therapeutics from $37.00 to $41.00 and gave the stock an “outperform” rating in a research report on Tuesday, January 20th. Citigroup boosted their price target on Beam Therapeutics from $64.00 to $68.00 and gave the stock a “buy” rating in a research report on Thursday, March 26th. Wedbush boosted their price target on Beam Therapeutics from $57.00 to $65.00 and gave the stock an “outperform” rating in a research report on Wednesday, February 25th. UBS Group began coverage on shares of Beam Therapeutics in a report on Wednesday, January 7th. They issued a “neutral” rating and a $28.00 price objective for the company. Finally, Wall Street Zen upgraded shares of Beam Therapeutics from a “sell” rating to a “hold” rating in a report on Saturday, February 28th. One analyst has rated the stock with a Strong Buy rating, eleven have assigned a Buy rating, three have given a Hold rating and one has assigned a Sell rating to the stock. Based on data from MarketBeat, the company has an average rating of “Moderate Buy” and a consensus price target of $49.36.

Read Our Latest Stock Report on BEAM

Beam Therapeutics Company Profile (Get Free Report)

Beam Therapeutics, Inc (NASDAQ: BEAM) is a biotechnology company dedicated to developing precision genetic medicines through its pioneering base editing platform. Headquartered in Cambridge, Massachusetts, with additional research facilities in Philadelphia, the company focuses on engineering molecular editors capable of making precise single-nucleotide changes in DNA. By harnessing its proprietary base editing technology, Beam aims to correct or disrupt disease-causing genetic variants at their source, offering the potential for novel therapies in areas with significant unmet medical need.

Founded in 2017 as a spin-out from Harvard University and the Broad and Whitehead Institutes, Beam was co-founded by leading academic researcher David R.

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2026-06-12 14:36 1mo ago
2026-04-11 09:20 3mo ago
Beam Therapeutics' CEO Sold Over 30,000 Company Shares. Here's What This Means for Investors.
BEAM Beam Therapeutics
FMP Stock News
Original source text
John M. Evans, CEO of Beam Therapeutics (BEAM +2.79%), executed an open-market sale of 30,078 shares on April 1, 2026, valued at approximately $739,000 according to the SEC Form 4 filing.

Transaction summaryMetricValueShares sold (direct)30,078Transaction value~$739,000Post-transaction shares (direct)1,047,205Post-transaction value (direct ownership)$25.36 millionTransaction value based on SEC Form 4 reported price ($24.58); post-transaction value based on April 1, 2026 market close ($24.22).

Key questionsHow does the size of this sale compare to Evans' recent selling activity?
The 30,078 shares sold is below the reported mean for Evans' sell-only transactions (~45,200 shares) and marks the smallest open-market sale in the last four disclosed sales, aligning with a declining direct share base.What is the impact of this sale on insider ownership and alignment?
After the transaction, Evans retains 1,047,205 direct shares and 103,000 indirect shares, with direct insider ownership now representing 1.03% of outstanding shares, sustaining a material equity interest.What was the price context for this transaction, and did it reflect a premium or discount to recent trading?
The shares were sold at around $24.58 per share, which was slightly above the April 1, 2026 closing price of $24.22 but below the closing price of $27.43 as of April 10, 2026.Does this transaction suggest a change in selling cadence or strategy?
The sale was executed under a pre-established Rule 10b5-1 trading plan, and the decrease in sale size is consistent with reduced direct share capacity from prior transactions rather than a shift in portfolio strategy.Company overviewMetricValuePrice (as of market close April 1, 2026)$24.22Market capitalization$2.79 billionRevenue (TTM)$139.74 million1-year price change60.84%* 1-year performance calculated using April 1, 2026 as the reference date.

Company snapshotBeam Therapeutics develops precision genetic medicines, including base editing therapies for sickle cell disease, beta thalassemia, T-cell acute lymphoblastic leukemia, and metabolic and rare genetic disorders.It has established multiple research collaborations and licensing agreements with pharmaceutical and biotechnology partners.The company targets patients with serious genetic diseases, with a focus on rare disease populations and partnerships with leading healthcare organizations.Beam Therapeutics is a clinical-stage biotechnology company specializing in the development of precision genetic medicines using base editing technology. The company's strategy centers on advancing a diversified pipeline of therapeutic candidates for hematologic, liver, and rare genetic disorders, leveraging collaborations with major industry players.

With a focus on innovation and strategic partnerships, Beam aims to address high unmet medical needs in the genetic medicine landscape.

What this transaction means for investorsBeam Therapeutics CEO John Evans’ April 1 sale of 30,078 company shares is not a warning sign for investors. The stock was sold to cover tax withholding obligations in connection with the vesting of restricted stock units.

The transaction comes at a time when  Beam Therapeutics stock surged due to positive clinical data related to its ristoglogene autogetemcel (risto-cel, formerly known as BEAM-101) treatment for sickle cell disease. The company exited 2025 with revenue of $139.7 million, up from 2024’s $63.5 million.

However, its 2025 research and development costs increased year over year to $409.6 million, resulting in a loss from operations of $383.7 million. Even so, this is a reduction compared to 2024’s operating loss of $415.6 million, which is an encouraging sign.

Moreover, the company ended 2025 with $1.2 billion in cash and marketable securities. This provides a robust sum to maintain operations as it progresses development of its treatments.

Robert Izquierdo has no position in any of the stocks mentioned. The Motley Fool has positions in and recommends Beam Therapeutics. The Motley Fool has a disclosure policy.
2026-06-12 14:36 1mo ago
2026-04-12 08:49 3mo ago
Colossal’s Ben Lamm Says Invasive Species Is a $5.4 Trillion Problem. Here’s His Solution
BEAM Beam Therapeutics
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.

Invasive species represent a $5.4 trillion global problem, with U.S. economic impact alone exceeding $500 billion annually. That’s according to Ben Lamm, CEO of Colossal Biosciences.

On episode 245 of the Moonshots with Peter Diamandis podcast, Lamm made the case that gene drive technology is the only scalable, humane answer.

“In New Zealand, in Australia, in parts of Africa, people are killing animals because they’re invasive species. They’re killing cats, they’re killing possums… that’s an animal welfare nightmare.”

Colossal’s proposed solution: genetically modified invasive animals that produce only male offspring, allowing populations to “live out their normal lives” before naturally dying out. No poison, no mass culling. Lamm also emphasized that Colossal’s proprietary gene drive technologies are “safer than what has ever been dispersed in the wild” and, critically, reversible: “we have the ability to roll it back.”

Texas has declared the screwworm a national emergency, with the pest currently spreading from Honduras through Mexico and threatening to “decimate our cattle and bison industry.” Diamandis noted the scale of the commercial opportunity: “dozens of species to be attacked and cost dozens of billions.”

Lamm’s broader point: 99% of synthetic biology and genome engineering talent focuses only on human healthcare, but the same technologies “apply to other use cases I think are even larger economically, but also have a bigger opportunity to help us.” He compared current invasive species control methods to “archaic ways of treating cancer versus what we know is here and what is coming.”

The Publicly Investable Gene-Editing Universe Colossal is private, so the question becomes where this thesis shows up in public markets. The three companies building the foundational CRISPR toolkit are CRISPR Therapeutics (NASDAQ:CRSP | CRSP Price Prediction), Beam Therapeutics (NASDAQ:BEAM), and Intellia Therapeutics (NASDAQ:NTLA).

CRISPR Therapeutics carries a $4.9 billion market cap with 17 analyst buy ratings and a consensus target of $83.35 against a current price of $51.22. Beam sits at $27.43 with 15 buy ratings and a $51.20 analyst target. Intellia, the smallest of the three at a $1.59 billion market cap, has surged 50% year-to-date to $13.49, with Phase 3 data on its lead HAE program expected mid-2026.

Their value here is as platform plays: the delivery systems, base editing precision, and in vivo editing capabilities they are refining for rare diseases are the same building blocks gene drive applications would require. If Lamm’s thesis proves out and gene drives move toward regulatory acceptance, these platforms become the infrastructure layer underneath it.

If gene drives become the standard, the companies that own the most precise, reversible genome editing platforms stand to benefit well beyond their current therapeutic pipelines. That’s the thread I’ll be watching.
2026-06-12 14:36 1mo ago
2026-04-27 07:06 2mo ago
3 Biotech Stocks That Could Benefit from the Patent Cliff
BEAM Beam Therapeutics
FMP Stock News
Original source text
Biotechnology stocks have seen a spike in merger and acquisition (M&A) activity. In March 2026 alone, there were 10 deals valued at approximately $31.5 billion.

A key reason for this activity is the upcoming patent cliff. This is the period when a drug loses its exclusive status and can face biosimilar competition. Analysts are forecasting that the industry faces a $300 billion patent cliff by 2030.

Two of the large-cap biopharma companies with best-selling drugs speeding toward the cliff are Merck & Co. NYSE: MRK with its blockbuster Keytruda drug and Bristol Myers Squibb NYSE: BMY with Eliquis. These are quality names that offer investors the safety of strong balance sheets and dividends.

Get CRISPR Therapeutics alerts:

There's an opportunity here for investors with an appetite for risk. That comes from the companies that could be future acquisition targets. These are companies that specialize in drugs that could change the biotech paradigm from chronic management to one-time cures.

Acquirable Assets: Which Biotechs Deserve a Higher FloorIt's not uncommon for every stock in a sector to move in tandem, but biotechnology right now requires a qualifier: the companies with the most potential are those with acquirable assets. Investors should look for three things:

The underlying science is differentiated enough that a large-cap company can’t quickly replicate it.

The company owns its intellectual property.

The drug/therapeutic has an indication that is large enough to move revenue and earnings for the acquiring company.

Many small-cap biotech names don’t meet every bar, which is only one reason this is such a tricky sector for investors. However, there are three names that investors should be watching. Each presents investors with an opportunity at a different point on the risk/maturity curve.

This isn’t predicting that these companies will be acquired. But because they check all three boxes above, as well as offer the promise of a potential one-time cure for chronic or untreatable diseases.

First-Mover Advantage in Gene EditingGene editing is a paradigm-shifting opportunity, and CRISPR Therapeutics NASDAQ: CRSP is an established pure play in the space. Unlike other names in this space, CRISPR already has a product in the market. In fact, CASGEVY delivered over $100 million in revenue in 2025. The company has also announced that patient initiations have nearly tripled year-over-year.

CRISPR Therapeutics Today

CRSP

CRISPR Therapeutics

$51.18 +0.94 (+1.88%)

As of 10:36 AM Eastern

This is a fair market value price provided by Massive. Learn more.

52-Week Range$40.00▼

$78.48Price Target$67.78

CASGEVY addresses sickle cell disease (SCD) and beta-thalassemia. Large, but relatively niche, markets. A key growth vector may come from its work in the cardiovascular space. The company’s CTX310 drug candidate is a potential one-and-done option for patients who need to quickly lower their triglyceride and LDL levels.

This is where the opportunity resides. CTX310 just delivered positive Phase 1 data. That means there’s still a runway to commercial approval, but the early results are positive.

Analysts are generally bullish on CRSP, but of the 19 analysts tracked by MarketBeat, the stock has two Sell ratings. Short interest is also around 24% as of this writing. That means investors may want to scale into a position gradually and use dips as times to be more aggressive.

High-Risk, High-Reward In Vivo EditingIf CRISPR Therapeutics represents the most commercially mature name in this space, Intellia Therapeutics NASDAQ: NTLA represents its highest stakes bet. Intellia is the pioneer of in vivo CRISPR editing. This means its therapies make edits directly inside the body rather than in a lab setting first. That distinction matters because it dramatically expands the range of diseases that gene editing can reach.

Intellia Therapeutics Today

NTLA

Intellia Therapeutics

$12.72 +0.37 (+2.98%)

As of 10:36 AM Eastern

This is a fair market value price provided by Massive. Learn more.

52-Week Range$7.95▼

$28.25Price Target$20.25

Intellia's two late-stage candidates are nexiguran ziclumeran (nex-z), developed in partnership with Regeneron for transthyretin amyloidosis (ATTR), and lonvoguran ziclumeran (lonvo-z), a wholly owned program targeting hereditary angioedema (HAE). Both are rare, underserved diseases where a one-time functional cure would represent a genuine paradigm shift from current chronic management.

The key 2026 catalysts are a Phase 3 data readout for lonvo-z in HAE, expected April 27, 2026, and progress in restarting and advancing its ATTR cardiomyopathy program after the FDA lifted the clinical hold. Either could move the stock materially in either direction. NTLA is not for the faint of heart, but for investors who believe in the in vivo thesis, this is the purest expression of it.

Precision Gene Editing’s Next FrontierWhere Intellia bets on CRISPR-Cas9, Beam Therapeutics NASDAQ: BEAM is pioneering something more precise. Its base editing technology works like a molecular pencil—rewriting a single genetic letter rather than making a double-strand cut in DNA. The technology has the potential to answer one of the persistent safety concerns that has kept some investors away from investing in gene editing stocks.

Beam Therapeutics Today

BEAM

Beam Therapeutics

$30.29 +0.88 (+3.00%)

As of 10:36 AM Eastern

This is a fair market value price provided by Massive. Learn more.

52-Week Range$15.60▼

$36.44Price Target$46.83

Beam's most advanced wholly owned program, BEAM-302, targets alpha-1 antitrypsin deficiency (AATD), a genetic disorder affecting the lungs and liver that currently has no curative treatment.

In March 2026, the company reported positive updated Phase 1/2 data and announced plans to advance into pivotal testing in the second half of the year. Its sickle cell program, risto-cel, could see a U.S. approval filing as early as late 2026.

Beam carries more early-stage risk than CRSP and faces nearer-term funding questions given its cash runway. But its differentiated platform and proximity to pivotal data make it a name worth monitoring for investors willing to take on that risk profile in exchange for the upside that a successful readout or acquisition offer could deliver.

Should You Invest $1,000 in CRISPR Therapeutics Right Now?Before you consider CRISPR Therapeutics, you'll want to hear this.

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While CRISPR Therapeutics currently has a Moderate Buy rating among analysts, top-rated analysts believe these five stocks are better buys.

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2026-06-12 14:36 1mo ago
2026-04-29 08:27 2mo ago
Jim Cramer: This Tech Stock Is A 'Winner', Snap Does Not Have Growth
BEAM Beam Therapeutics
FMP Stock News
Original source text
As per recent news, Ondas completed its merger with U.S. defense prime contractor Mistral on April 24 in a $175 million deal, adding programs exceeding $1 billion and expanding direct prime participation across U.S. Department of War programs.

Cramer said he likes Halliburton Co (NYSE:HAL) very much as it has been a “good stock even in a bad oil market, so it's been a great stock in a good oil market.”

Lending support to his choice, Halliburton, on April 21, reported better-than-expected first-quarter financial results.

Nokia Oyj (NYSE:NOK) is a “winner,” Cramer said.

Cramer said he is a growth buyer, and Snap (NYSE:SNAP) does not have growth.

The Mad Money host said he likes Cameco Corporation (NYSE:CCJ) because it's a real uranium company.

When asked about Harley-Davidson Inc (NYSE:HOG), he said, “The technology is absolutely terrific, but the actual earnings, they're just blah. I can't go for it.”

Price Action:

Photo: katz / Shutterstock.com

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2026-06-12 14:36 1mo ago
2026-04-29 14:10 2mo ago
Concurrent Investment Advisors LLC Invests $2.13 Million in Beam Therapeutics Inc. $BEAM
BEAM Beam Therapeutics
FMP Stock News
Original source text
Posted by Defense World Staff on Apr 29th, 2026

Concurrent Investment Advisors LLC acquired a new stake in Beam Therapeutics Inc. (NASDAQ:BEAM – Free Report) in the 4th quarter, according to its most recent disclosure with the Securities and Exchange Commission. The firm acquired 76,825 shares of the company’s stock, valued at approximately $2,130,000. Concurrent Investment Advisors LLC owned approximately 0.08% of Beam Therapeutics at the end of the most recent reporting period.

Several other hedge funds have also recently bought and sold shares of the company. CWM LLC increased its stake in Beam Therapeutics by 15.4% in the 4th quarter. CWM LLC now owns 2,466 shares of the company’s stock valued at $68,000 after purchasing an additional 329 shares in the last quarter. Wealth Effects LLC increased its stake in Beam Therapeutics by 4.3% in the 4th quarter. Wealth Effects LLC now owns 9,600 shares of the company’s stock valued at $266,000 after purchasing an additional 400 shares in the last quarter. Arizona State Retirement System increased its stake in Beam Therapeutics by 2.2% in the 3rd quarter. Arizona State Retirement System now owns 26,771 shares of the company’s stock valued at $650,000 after purchasing an additional 580 shares in the last quarter. Van ECK Associates Corp increased its stake in Beam Therapeutics by 48.7% in the 3rd quarter. Van ECK Associates Corp now owns 2,158 shares of the company’s stock valued at $52,000 after purchasing an additional 707 shares in the last quarter. Finally, Mirae Asset Global Investments Co. Ltd. increased its stake in Beam Therapeutics by 26.1% in the 4th quarter. Mirae Asset Global Investments Co. Ltd. now owns 4,931 shares of the company’s stock valued at $137,000 after purchasing an additional 1,020 shares in the last quarter. 99.68% of the stock is owned by hedge funds and other institutional investors.

Insider Transactions at Beam Therapeutics In other news, insider Christine Bellon sold 5,956 shares of Beam Therapeutics stock in a transaction dated Wednesday, April 1st. The stock was sold at an average price of $24.58, for a total transaction of $146,398.48. Following the sale, the insider directly owned 109,711 shares of the company’s stock, valued at approximately $2,696,696.38. The trade was a 5.15% decrease in their ownership of the stock. The sale was disclosed in a legal filing with the Securities & Exchange Commission, which can be accessed through this hyperlink. The transaction was executed under a pre-arranged Rule 10b5-1 trading plan. The sale was made to cover tax withholding obligations related to the vesting of equity awards. Also, CEO John M. Evans sold 30,078 shares of Beam Therapeutics stock in a transaction dated Wednesday, April 1st. The stock was sold at an average price of $24.58, for a total value of $739,317.24. Following the sale, the chief executive officer directly owned 1,047,205 shares in the company, valued at approximately $25,740,298.90. The trade was a 2.79% decrease in their ownership of the stock. The SEC filing for this sale provides additional information. The transaction was executed under a pre-arranged Rule 10b5-1 trading plan. The sale was made to cover tax withholding obligations related to the vesting of equity awards. Insiders have sold a total of 79,544 shares of company stock worth $1,899,942 over the last ninety days. 3.50% of the stock is owned by insiders.

Wall Street Analyst Weigh In BEAM has been the subject of several research analyst reports. UBS Group started coverage on Beam Therapeutics in a research note on Wednesday, January 7th. They issued a “neutral” rating and a $28.00 price objective for the company. Wedbush increased their target price on Beam Therapeutics from $57.00 to $65.00 and gave the company an “outperform” rating in a report on Wednesday, February 25th. Sanford C. Bernstein increased their target price on Beam Therapeutics from $37.00 to $41.00 and gave the company an “outperform” rating in a report on Tuesday, January 20th. Canaccord Genuity Group started coverage on Beam Therapeutics in a report on Friday, February 20th. They set a “buy” rating and a $74.00 target price on the stock. Finally, Tudor Pickering set a $41.00 target price on Beam Therapeutics in a report on Wednesday, January 21st. One investment analyst has rated the stock with a Strong Buy rating, eleven have given a Buy rating, three have assigned a Hold rating and one has given a Sell rating to the stock. According to MarketBeat, the company has a consensus rating of “Moderate Buy” and an average price target of $49.36.

Get Our Latest Research Report on Beam Therapeutics

Beam Therapeutics Trading Up 4.8% Shares of Beam Therapeutics stock opened at $30.56 on Wednesday. Beam Therapeutics Inc. has a twelve month low of $15.35 and a twelve month high of $36.44. The stock has a market capitalization of $3.14 billion, a P/E ratio of -30.26 and a beta of 2.18. The business’s fifty day moving average price is $27.03 and its 200 day moving average price is $26.91.

Beam Therapeutics (NASDAQ:BEAM – Get Free Report) last issued its earnings results on Tuesday, February 24th. The company reported $2.33 earnings per share for the quarter, beating analysts’ consensus estimates of ($1.13) by $3.46. Beam Therapeutics had a negative return on equity of 30.65% and a negative net margin of 57.24%.The firm had revenue of $114.11 million for the quarter, compared to analysts’ expectations of $13.22 million. During the same quarter last year, the firm earned ($1.09) earnings per share. The firm’s revenue for the quarter was up 280.3% compared to the same quarter last year. As a group, sell-side analysts predict that Beam Therapeutics Inc. will post -3.9 EPS for the current year.

About Beam Therapeutics (Free Report)

Beam Therapeutics, Inc (NASDAQ: BEAM) is a biotechnology company dedicated to developing precision genetic medicines through its pioneering base editing platform. Headquartered in Cambridge, Massachusetts, with additional research facilities in Philadelphia, the company focuses on engineering molecular editors capable of making precise single-nucleotide changes in DNA. By harnessing its proprietary base editing technology, Beam aims to correct or disrupt disease-causing genetic variants at their source, offering the potential for novel therapies in areas with significant unmet medical need.

Founded in 2017 as a spin-out from Harvard University and the Broad and Whitehead Institutes, Beam was co-founded by leading academic researcher David R.

Further Reading Five stocks we like better than Beam Therapeutics Want to see what other hedge funds are holding BEAM? Visit HoldingsChannel.com to get the latest 13F filings and insider trades for Beam Therapeutics Inc. (NASDAQ:BEAM – Free Report).

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2026-06-12 14:36 1mo ago
2026-05-07 07:00 2mo ago
Beam Therapeutics Reports First Quarter 2026 Financial Results and Recent Business Updates
BEAM Beam Therapeutics
FMP Stock News
Original source text
Recent BEAM-302 Topline Data in Alpha-1 Antitrypsin Deficiency (AATD) Demonstrate Strong Single-dose Safety and Efficacy Profile, with 60 mg Selected as Optimal Biological Dose; Global Pivotal Cohort Expected to Initiate in Second Half of 2026 Data from Phase 1/2 BEACON Clinical Trial of Risto-cel in Sickle Cell Disease Published in April 1 Issue of the New England Journal of Medicine; U.S. Biologics License Application (BLA) Submission Expected as Early as Year-End 2026 Investigational New Drug (IND) Application for BEAM-304 in PKU and Data from BEAM-301 in GSDIa Anticipated in 2026 Ended First Quarter 2026 with $1.2 Billion in Cash, Cash Equivalents and Marketable Securities; Cash Runway Expected to Support Operating Plans into mid-2029 CAMBRIDGE, Mass., May 07, 2026 (GLOBE NEWSWIRE) --   Beam Therapeutics Inc. (Nasdaq: BEAM), a biotechnology company developing precision genetic medicines through base editing, today reported first quarter 2026 financial results and provided updates across the company's hematology and genetic disease franchises.
2026-06-12 14:36 1mo ago
2026-05-07 09:56 2mo ago
Beam Therapeutics Inc. (BEAM) Reports Q1 Loss, Beats Revenue Estimates
BEAM Beam Therapeutics
FMP Stock News
Original source text
Beam Therapeutics Inc. (BEAM - Free Report) came out with a quarterly loss of $0.91 per share versus the Zacks Consensus Estimate of a loss of $0.87. This compares to a loss of $1.24 per share a year ago. These figures are adjusted for non-recurring items.

This quarterly report represents an earnings surprise of -4.60%. A quarter ago, it was expected that this company would post a loss of $1.13 per share when it actually produced a loss of $0.1, delivering a surprise of +91.15%.

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

Beam Therapeutics, which belongs to the Zacks Medical - Biomedical and Genetics industry, posted revenues of $31.74 million for the quarter ended March 2026, surpassing the Zacks Consensus Estimate by 52.44%. This compares to year-ago revenues of $7.47 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.

Beam Therapeutics shares have added about 16.7% since the beginning of the year versus the S&P 500's gain of 7.6%.

What's Next for Beam Therapeutics?While Beam 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 Beam 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 -$0.89 on $20.82 million in revenues for the coming quarter and -$3.90 on $83.26 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 40% 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, Kyntra Bio (KYNB - Free Report) , is yet to report results for the quarter ended March 2026. The results are expected to be released on May 11.

This biotech drug developer is expected to post quarterly loss of $3.36 per share in its upcoming report, which represents a year-over-year change of +16%. The consensus EPS estimate for the quarter has remained unchanged over the last 30 days.

Kyntra Bio's revenues are expected to be $1.56 million, down 43.3% from the year-ago quarter.
2026-06-12 14:36 1mo ago
2026-05-08 13:11 2mo ago
BEAM's Q1 Loss Wider Than Expected, Revenues Beat Estimates
BEAM Beam Therapeutics
FMP Stock News
Original source text
Key Takeaways Beam Therapeutics posted Q1 revenues of $31.7M, topping estimates as collaboration revenues increased.BEAM plans a 2026 BLA filing for risto-cel after updated SCD study data showed progress.BEAM-302 showed durable AAT increases in AATD, with pivotal cohort enrollment set for 2H'26. Beam Therapeutics (BEAM - Free Report) incurred a loss of 91 cents per share in the first quarter of 2026, wider than the Zacks Consensus Estimate of a loss of 87 cents. The company had reported a loss of $1.23 per share in the year-ago quarter.

Revenues totaled $31.7 million, beating the Zacks Consensus Estimate of $21 million. The company had recorded revenues of $7.4 million in the year-ago quarter. The top line primarily comprises license and collaboration revenues.

Year to date, shares of Beam Therapeutics have risen 13.5% against the industry’s 0.2% decline.

Image Source: Zacks Investment Research

BEAM's Q1 Results in DetailResearch and development expenses were $104.5 million in the first quarter, up 5.8% from the year-ago quarter.

General and administrative expenses surged 23.2% year over year to $34.4 million.

As of March 31, 2026, Beam Therapeutics had cash, cash equivalents and marketable securities worth $1.21 billion compared with $1.25 billion as of Dec. 31, 2025. The company expects its cash position, including the initial $100 million received and an anticipated additional $100 million from its financing agreement with Sixth Street, to support operations into mid-2029.

BEAM's Pipeline UpdatesBeam Therapeutics 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, an inherited blood disorder.

The company presented updated data from the BEACON study in December 2025, which continued to show evidence of risto-cel’s differentiated treatment profile in SCD patients. BEAM plans to submit a biologics licensing application (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 (GSD1a) and alpha-1 antitrypsin deficiency (AATD), respectively.

BEAM-301 is being evaluated in a phase I/IIdose-exploration study in patients with GSDIa. Initial data from the study are expected in 2026.

The company is developing BEAM-302 in an ongoing phase I/II dose-escalation study for the treatment of AATD. In March, BEAM announced positive updated data from the study showing that BEAM-302 produced durable increases in functional AAT levels, significant reductions in mutant Z-AAT and generation of corrected M-AAT with a favorable safety profile across single doses up to 75 mg.

Following the FDA feedback, Beam Therapeutics aims to pursue an accelerated approval pathway for BEAM-302 and plans to initiate a global pivotal expansion cohort in the second half of 2026. The study is expected to enroll around 50 additional patients with AATD-related lung disease to support a future BLA filing.

Dosing in the ongoing phase I healthy volunteer study, evaluating BEAM-103, an anti-CD117 monoclonal antibody for the treatment of SCD, is expected to be completed in the first half of 2026.

The company expanded its liver-targeted genetic disease franchise with BEAM-304 for the treatment of phenylketonuria and plans to file an investigational new drug application with the FDA in 2026.

BEAM’s Zacks Rank & Stocks to ConsiderBeam Therapeutics currently carries a Zacks Rank #4 (Sell).

Some better-ranked stocks in the biotech sector are Amarin Corporation (AMRN - Free Report) , Indivior Pharmaceuticals (INDV - Free Report) and Liquidia Corporation (LQDA - Free Report) , each 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 5.9% 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 10.4% year to date.

Indivior Pharmaceuticals’ earnings beat estimates in each of the trailing four quarters, with the average surprise being 65.44%.

Over the past 60 days, estimates for Liquidia’s 2026 earnings per share have declined from $2.14 to $1.75. Over the same period, EPS estimates for 2027 have decreased from $3.79 to $2.91. LQDA shares have gained 22.6% year to date.

Liquidia’s earnings beat estimates in two of the trailing four quarters, while missing the same on the remaining occasions, with the average surprise being 39.38%.
2026-06-12 14:36 1mo ago
2026-05-12 09:30 2mo ago
Beam Therapeutics to Present Updated Biomarker Data from Phase 1/2 BEACON Trial Further Underscoring Risto-cel's Ability to Restore Red Blood Cell Health and Function in Sickle Cell Disease at EHA2026
BEAM Beam Therapeutics
FMP Stock News
Original source text
CAMBRIDGE, Mass., May 12, 2026 (GLOBE NEWSWIRE) -- Beam Therapeutics Inc. (Nasdaq: BEAM), a biotechnology company developing precision genetic medicines through base editing, today announced that the company will present updated biomarker data from the BEACON Phase 1/2 clinical trial of ristoglogene autogetemcel (risto-cel) in sickle cell disease (SCD) at the European Hematology Association 2026 Congress (EHA2026), taking place June 11-14, 2026, in Stockholm, Sweden. Risto-cel is an investigational autologous cell therapy with a potential best-in-class profile for the treatment of SCD.
2026-06-12 14:36 1mo ago
2026-05-13 07:00 2mo ago
Beam Therapeutics to Present at 2026 RBC Capital Markets Global Healthcare Conference
BEAM Beam Therapeutics
FMP Stock News
Original source text
May 13, 2026 07:00 ET  | Source: Beam Therapeutics

CAMBRIDGE, Mass., May 13, 2026 (GLOBE NEWSWIRE) -- Beam Therapeutics Inc. (Nasdaq: BEAM), a biotechnology company developing precision genetic medicines through base editing, today announced that John Evans, chief executive officer of Beam, will present at the 2026 RBC Capital Markets Healthcare Conference on Wednesday, May 20, 2026, at 10:30 a.m. ET in New York.

The live webcast will be available in the investor section of the company's website at www.beamtx.com and will be archived for 60 days following the presentation.

About Beam Therapeutics
Beam Therapeutics (Nasdaq: BEAM) is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Beam’s suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing life-long cures to patients suffering from serious diseases.

Contact:

Holly Manning
Beam Therapeutics
[email protected]
2026-06-12 14:36 1mo ago
2026-05-13 09:46 2mo ago
Beam Therapeutics: Base Editing Is Moving From Platform Story To Regulatory Asset Story
BEAM Beam Therapeutics
FMP Stock News
Original source text
Beam Therapeutics is transitioning from a scientific platform to a late-stage genetic medicine company with a clear commercial bridge. BEAM's $1.2B cash position supports a runway into mid-2029, enabling pivotal programs in sickle cell disease (Risto-cel) and AATD (BEAM-302). Risto-cel targets process efficiency and efficacy in SCD, with a potential BLA submission by year-end 2026; BEAM-302 pursues accelerated approval in AATD.
2026-06-12 14:35 1mo ago
2026-05-13 11:49 2mo ago
Beam Therapeutics Supports AlphaDetect to Accelerate Detection of Alpha-1
BEAM Beam Therapeutics
FMP Stock News
Original source text
The sponsorship helps expand proven strategies to consistently detect a genetic, irreversible, and progressive condition in patients with liver and/or lung disease.

, /PRNewswire/ -- AlphaDetect, the nonprofit organization powered and funded by the Alpha-1 Foundation (A1F), today announced Beam Therapeutics as an inaugural industry sponsor. The support further strengthens efforts to accelerate routine targeted detection of Alpha-1 Antitrypsin Deficiency (Alpha-1) in people impacted by liver and/or lung disease, consistent with clinical practice guidelines.

Beam Therapeutics AlphaDetect is dedicated to identifying everyone at risk for this progressive, irreversible genetic condition by elevating awareness and removing barriers to detection. The organization will provide free genetic testing for alpha-1 in their proprietary laboratory, at no cost to insurance or patients. In addition, they provide support from a committed engagement team for healthcare providers. These efforts will increase the availability of Alpha-1 detection tools and support at the practice level while also partnering with healthcare providers to strategically advance protocols and technologies across healthcare systems.

"Advancing Alpha-1 detection requires a focused effort," said Amy Simon, MD, Chief Medical Officer of Beam Therapeutics. "Working with the Alpha-1 Foundation, and now AlphaDetect as a subsidiary of A1F, there is an opportunity to accelerate detection across the Alpha-1 community aligned with clinical guidelines. These efforts will help bring much needed answers to patients and their families. As one of the inaugural sponsors of this effort, we're proud to have closely collaborated with AlphaDetect on this shared goal of increasing awareness and testing for Alpha-1."

"Alpha-1 is a progressive, genetic lung and liver condition where delays in detection may have real, irreversible consequences," said Julie Murray, CEO of AlphaDetect. "The ability to scale proven approaches to identifying at-risk patients, quickly and systematically, can inform timely decisions for those impacted. The support and commitment from Beam Therapeutics are important and appreciated as we continue to advance Alpha-1 detection."

Alpha-1 remains significantly underdiagnosed, with more than 90% of affected individuals estimated to be unidentified. It is also the leading known genetic risk factor for COPD and is associated with liver disease in both children and adults. Importantly, detection also provides a point of entry into the Alpha-1 community, opening the door to the comprehensive information, support, and resources needed for the journey ahead.

"This support builds on Beam Therapeutic's commitment to progressive clinical research to support the Alpha-1 community and represents an important step forward in how we approach detection," said Scott Santarella, CEO of the Alpha-1 Foundation. "By expanding these efforts through AlphaDetect, we can identify more individuals earlier and deliver on A1F's mission of improving their lives."

The latest clinical guidelines recommend testing for Alpha-1 in all individuals with COPD, treatment-resistant asthma, or unexplained liver disease. Yet real-world results fall far short of this. AlphaDetect is committed to closing the gap. Beam Therapeutics sponsorship and commitment will help AlphaDetect scale efforts to enhance provider education, broaden detection strategies, and work across the Alpha-1 community to identify individuals with Alpha-1.

About AlphaDetect 

AlphaDetect, founded in 2025, accelerates detection to uncover everyone genetically at risk for Alpha-1. Located in Durham, NC, AlphaDetect will operate as a limited liability company and a non-profit subsidiary of Alpha-1 Foundation, holding tax-exempt status under Section 501(c)3 of the Internal Revenue Code. 

For more information, visit https://alpha1.org/alphadetect/

Contact: Cindy Machles

917-453-9760

Email: [email protected]

About Beam Therapeutics
Beam Therapeutics (Nasdaq: BEAM) is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Beam's suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of potential therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing lifelong cures to patients suffering from serious diseases.

For more information, visit beamtx.com

Contact: Holly Manning

Vice President, Investor Relations and External Communications

857-327-9449

[email protected]

About the Alpha-1 Foundation

The Alpha-1 Foundation, founded in 1995, is committed to finding a cure for Alpha-1 Antitrypsin Deficiency (Alpha-1) and to improving the lives of people affected by the condition worldwide. A1F has invested over $100 million to support Alpha-1 research and programs at 130 institutions in North America, Europe, the Middle East and Australia.

For more information, visit alpha1.org

Contact: Jeanne Kushner

Senior Director of Communications & Policy

877-228-7321

[email protected] 

SOURCE Alpha-1 Foundation
2026-06-12 14:35 1mo ago
2026-05-13 12:00 2mo ago
Beam Therapeutics Supports AlphaDetect to Accelerate Detection of Alpha-1
BEAM Beam Therapeutics
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Beam Therapeutics Supports AlphaDetect to Accelerate Detection of Alpha-1 PR Newswire DURHAM, N.C., May 13, 2026
2026-06-12 14:35 1mo ago
2026-05-18 14:05 2mo ago
Hedge Fund Drops $40 Million on Gene-Editing Biotech Beam. Is It a Buy?
BEAM Beam Therapeutics
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On May 15, 2026, ADAR1 Capital Management disclosed a new position in Beam Therapeutics (BEAM +2.79%), acquiring 1,446,375 shares in an estimated $40.13 million trade based on quarterly average pricing.

What happenedAccording to a Securities and Exchange Commission (SEC) filing dated May 15, 2026, ADAR1 Capital Management, opened a new position in Beam Therapeutics, buying 1,446,375 shares. The estimated transaction value, based on the average closing price for the January–March 2026 quarter, was $40.13 million. At quarter end, the position was valued at $34.47 million, reflecting both the purchase and price changes.

What else to knowThis was a new position for the fund, making up 2.03% of 13F reportable assets as of March 31, 2026.Top five holdings after the filing:NASDAQ: ABVX: $155.22 million (9.4% of AUM)NASDAQ: PTGX: $104.78 million (6.4% of AUM)NASDAQ: ROIV: $91.02 million (5.5% of AUM)NASDAQ: IMVT: $66.55 million (4.0% of AUM)NYSEMKT: SPY: $49.39 million (3.0% of AUM)As of May 15, 2026, Beam Therapeutics shares were priced at $27.93, up 61.9% over the past year, outperforming the S&P 500 by 36.7 percentage points.Company overviewMetricValuePrice (as of market close May 15, 2026)$27.93Market Capitalization$2.87 billionRevenue (TTM)$164.01 millionNet Income (TTM)($65.04 million)Company snapshotDevelops precision genetic medicines targeting serious diseases, with lead candidates addressing sickle cell disease, beta thalassemia, T-cell acute lymphoblastic leukemia, and glycogen storage disorders.Operates a biotechnology business model focused on research, development, and commercialization of gene-editing therapies, generating revenue through product development, strategic collaborations, and licensing agreements.Serves patients with severe genetic and rare diseases, partnering with healthcare providers, research institutions, and pharmaceutical companies in the United States and globally.Beam Therapeutics is a biotechnology company specializing in precision genetic medicines, leveraging base editing technology to address a range of serious genetic disorders. The company advances a diversified pipeline through both proprietary research and strategic collaborations with leading academic and industry partners. With a focus on innovation and targeted therapies, Beam Therapeutics aims to establish a competitive position in the rapidly evolving field of gene editing.

Today's Change

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What this transaction means for investorsInvesting in pre-commercial gene therapy means betting on science that hasn't reached patients yet. You're wagering the technology works, clinical trials succeed, and the FDA approves before the cash runs out. ADAR1 Capital Management made that bet with a $40 million Beam Therapeutics position in Q1.

Beam develops gene-editing therapies for rare diseases but has no approved drugs yet. It has $1.2 billion in cash and burns around $140 million quarterly on R&D. Revenue comes entirely from collaboration milestone payments, not product sales.

The company expects to file for FDA approval of risto-cel (a sickle cell treatment) by late 2026 and will start pivotal trials for BEAM-302 (treating a rare genetic liver disease) in the second half of 2026. Both programs have shown promising early data and potential accelerated approval pathways.

For average investors, this is speculative biotech investing. The upside is significant if one or both drugs get approved and gain market traction. The risk is clinical trial failures, regulatory setbacks, or manufacturing issues derailing the pathway to profitability. Gene therapy is high-reward science with high execution risk.

Sara Appino has no position in any of the stocks mentioned. The Motley Fool has positions in and recommends Beam Therapeutics. The Motley Fool recommends Protagonist Therapeutics and Roivant Sciences. The Motley Fool has a disclosure policy.
2026-06-12 14:35 1mo ago
2026-05-18 16:00 2mo ago
Beam Therapeutics Presents Recently Reported Topline Clinical Data for BEAM-302 in Alpha-1 Antitrypsin Deficiency (AATD) at the American Thoracic Society (ATS) 2026 International Conference
BEAM Beam Therapeutics
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Presentation Features Additional Data from the Single-dose Cohorts of the Phase 1/2 Trial, Including Detailed Safety Results, Efficacy Durability and Reduction in Human Neutrophil Elastase Activity Post-BEAM-302 Treatment May 18, 2026 16:00 ET  | Source: Beam Therapeutics

CAMBRIDGE, Mass., May 18, 2026 (GLOBE NEWSWIRE) -- Beam Therapeutics Inc. (Nasdaq: BEAM), a biotechnology company developing precision genetic medicines through base editing, today presented the recently reported clinical data from the BEAM-302 Phase 1/2 trial in alpha-1 antitrypsin deficiency (AATD) at a symposium on translating scientific discovery in gene editing into clinical progress for patients with lung disease. The presentation was given by Amy Simon, M.D., chief medical officer of Beam, at the American Thoracic Society (ATS) International Conference being held in Orlando, Fla.

“At Beam, we are committed to leading innovation in the AATD community, with a goal of transforming disease outcomes for all patients suffering from this disease,” said Dr. Simon. “For BEAM-302, the data shared today build on the growing body of clinical evidence that supports the profound impact of treating AATD at the root cause of disease, the DNA mutation, with this one-time investigational therapy. We are rapidly executing toward pivotal development to deliver BEAM-302 to patients with AATD as safely and expeditiously as possible. Our long-term goal is to combine our growing understanding of AATD biology and our leading gene editing capabilities to maximize patient benefit across the entire spectrum of disease manifestations. We are also continuing to expand our cross-sector collaborations with leading AATD advocacy organizations to advance disease awareness and increase diagnosis, support the evolution of research approaches and incorporate patient perspectives across the broader scientific and care community.”

“The ongoing results from the BEAM-302 trial are truly remarkable, suggesting a single treatment dose can correct AATD at its root cause and durably restore normal AAT function, addressing both lung and liver manifestations of disease over a patient's entire lifetime,” said John Hurst, M.D., Ph.D., professor at the University College London and an investigator in the BEAM-302 trial. “This is not only a paradigm shift for the treatment of AATD, but also for medicine more widely as we enter the era of gene correction as a tool for clinicians.”

BEAM-302 is being evaluated in a Phase 1/2, open-label, dose exploration and dose expansion clinical trial to investigate its safety, tolerability, pharmacodynamics, pharmacokinetics and efficacy. Topline data from 29 patients treated with BEAM-302 as of a February 10, 2026 data cutoff date were reported in March 2026. Dr. Simon's presentation at ATS features additional data for the single-dose cohorts from the same data cutoff, including detailed safety results, efficacy durability and reduction in human neutrophil elastase activity (a direct measure of AAT function) post-BEAM-302 treatment. Dr. Simon’s presentation is available on the “Presentations and Publications” section of Beam’s website at beamtx.com.

Based on feedback from the U.S. Food and Drug Administration (FDA), Beam intends to pursue an accelerated approval pathway for BEAM-302. To support a future biologics licensing application (BLA) submission, the company anticipates enrolling approximately 50 additional patients with AATD-associated lung disease, with or without liver disease, in an expansion of the ongoing open-label Phase 1/2 trial. Beam expects to initiate this pivotal cohort in the second half of 2026. In addition, Beam expects to present detailed and updated BEAM-302 data at a medical congress in 2026.

About BEAM-302
BEAM-302 is a liver-targeting lipid-nanoparticle (LNP) formulation of base editing reagents designed to correct the PiZ mutation. Patients homozygous for this mutation (PiZZ) represent the majority of patients living with severe AATD disease. A one-time A-to-G correction of the PiZ mutation with Beam’s adenine base editor has the potential to simultaneously reduce the aggregation of mutant, misfolded AAT protein that causes toxicity to the liver (Z-AAT), generate therapeutic levels of corrected protein (M-AAT), and increase total and functional AAT in circulation, thereby addressing the underlying pathophysiology of both the liver and lung disease. In addition, the reduction in circulating PiZ has the potential to further minimize lung inflammation and dysfunction. Importantly, because BEAM-302 corrects the native AAT gene in its normal genetic location, AAT levels have been observed to increase physiologically in response to infection and inflammation in treated patients. This is a critical aspect of AAT’s normal function to regulate the body’s inflammatory response, which does not occur with currently approved protein replacement therapies. Correction of the PiZ mutation has been durable in patients treated in Beam's clinical trial.

About Alpha-1 Antitrypsin Deficiency (AATD)
AATD is an inherited genetic disorder that can cause early onset emphysema and liver disease. The most severe and common form of AATD arises when a patient has a point mutation in both copies of the SERPINA1 gene at amino acid 342 position (E342K, also known as the PiZ mutation or the “Z” allele). This point mutation causes alpha-1 antitrypsin, or AAT, to misfold, accumulating inside liver cells rather than being secreted, resulting in very low levels (10%-15%) of circulating AAT. In addition to resulting in lower levels, the PiZ AAT protein variant is also less enzymatically effective compared to wildtype AAT protein (also known as the “M” allele). As a consequence, the lung is left unprotected from neutrophil elastase, resulting in progressive, destructive changes in the lung, such as emphysema, which can result in the need for lung transplant. The mutant AAT protein also accumulates in the liver, causing liver inflammation and cirrhosis, which can ultimately cause liver failure or cancer requiring patients to undergo a liver transplant. It is estimated that more than 100,000 individuals in the U.S. have two copies of the Z allele, known as the PiZZ genotype, although only about 10% of all patients are thought to have been diagnosed. Although augmentation therapy has been approved in the U.S. for the treatment of AATD-associated lung disease, there are currently no curative treatments and significant unmet need exists for patients with AATD.

About Beam Therapeutics
Beam Therapeutics (Nasdaq: BEAM) is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Beam’s suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of potential therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing lifelong cures to patients suffering from serious diseases.

Cautionary Note Regarding Forward-Looking Statements
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Investors are cautioned not to place undue reliance on these forward-looking statements, including, but not limited to, statements related to: the therapeutic applications and potential of our technology, including with respect to AATD; our plans, and anticipated timing, to advance our AATD program; the clinical trial designs and expectations for BEAM-302; our anticipated regulatory interactions and filings; and our ability to develop lifelong, curative, precision genetic medicines for patients through base editing. Each forward-looking statement is subject to important risks and uncertainties that could cause actual results to differ materially from those expressed or implied in such statement, including, without limitation, risks and uncertainties related to: our ability to develop, obtain regulatory approval for, and commercialize our product candidates, which may take longer or cost more than planned; our ability to raise additional funding, which may not be available; our ability to obtain, maintain and enforce patent and other intellectual property protection for our product candidates; the uncertainty that our product candidates will receive regulatory approval necessary to initiate or continue human clinical trials; that preclinical testing of our product candidates and preliminary or interim data from preclinical studies and clinical trials may not be predictive of the results or success of ongoing or later clinical trials; that initiation and enrollment of, and anticipated timing to advance, our clinical trials may take longer than expected; that our product candidates, including the delivery modalities we rely on to administer them, may cause serious adverse events; that our product candidates may experience manufacturing or supply interruptions or failures; risks related to competitive products; and the other risks and uncertainties identified under the headings “Risk Factors Summary” and “Risk Factors” in our Annual Report on Form 10-K for the year ended December 31, 2025, our Quarterly Report on Form 10-Q for the quarter ended March 31, 2026, and in any subsequent filings with the Securities and Exchange Commission. These forward-looking statements speak only as of the date of this press release. Factors or events that could cause our actual results to differ may emerge from time to time, and it is not possible for us to predict all of them. We undertake no obligation to update any forward-looking statement, whether as a result of new information, future developments or otherwise, except as may be required by applicable law.

Contacts:

Investors:
Holly Manning
Beam Therapeutics
[email protected]

Media:
Josie Butler
1AB
[email protected]
2026-06-12 14:35 1mo ago
2026-05-20 14:05 2mo ago
Beam Therapeutics Eyes Sickle Cell BLA as Alpha-1 Gene-Editing Program Advances
BEAM Beam Therapeutics
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3 Biotech Stocks That Could Benefit from the Patent CliffBeam Therapeutics NASDAQ: BEAM Chief Executive Officer John Evans said the company is advancing its base-editing platform across hematology and liver disease programs, with a potential biologics license application for its sickle cell disease candidate possible as early as the end of this year.

Speaking at RBC Capital Markets’ Global Healthcare Conference in a discussion with Senior Biotechnology Research Analyst Luca Issi, Evans described Beam as a “next-generation gene-editing company” focused on base editing, a form of CRISPR designed to make permanent single-letter changes in genes without creating a double-strand break.

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MarketBeat Week in Review – 3/4 – 3/8Evans said that distinction could allow Beam to make “more therapeutic edits” and “more precise edits,” including correcting mutations back to normal rather than only knocking genes out.

Alpha-1 Program Shows Dose Selection Progress A major focus of the discussion was BEAM-302, Beam’s program for alpha-1 antitrypsin deficiency. Evans said the program is designed to correct the single-letter misspelling in the alpha-1 gene back to normal, which he said is the first time anyone has been able to do so.

Beam Therapeutics Bolts Higher on Gene Therapy Licensing PaymentsEvans said earlier data showed that a 60-milligram dose achieved alpha-1 levels above 11 micromolar, a threshold he described as important because carriers who do not have the disease generally live above that line, while patients with progressive lung and liver damage are usually below it.

According to Evans, additional dose exploration around 60 milligrams, including a 75-milligram dose and a two-dose 60-milligram regimen, did not produce meaningful additional pharmacodynamic benefit. He said the results confirmed that 60 milligrams is the dose Beam wants to use.

Evans said the larger data set showed the 60-milligram dose produced an average alpha-1 level of 16 micromolar, with normal M protein levels above 90% and Z protein reduced by 84%.

“We had clearly and dramatically changed the disease physiology to at least a carrier physiology,” Evans said, adding that this supports Beam’s view that treated patients should not experience progressive disease going forward.

Safety and Redosing Discussed Issi asked about tolerability of a second 60-milligram dose, which Evans said was not as well tolerated as the first. Evans said it was difficult to know why, noting that preclinical data suggested eight weeks should have been enough time for the first lipid nanoparticle dose to clear. However, he said alpha-1 livers may differ in physiology and macrophage biology, potentially retaining some sensitivity.

Evans characterized the observed events as manageable. He said Beam saw higher infusion-related reactions, such as grade two events treated with Motrin, and one patient with a grade three AST/ALT elevation that was asymptomatic, did not require hospitalization, did not involve bilirubin changes and resolved quickly.

Evans said he did not believe the findings indicate that lipid nanoparticle redosing is not possible. He noted that Beam still plans to redose patients who previously received subtherapeutic 15-milligram and 30-milligram doses with the selected 60-milligram dose.

On liver enzyme elevations, Evans said the pattern Beam observed was consistent with a “classic LNP signal,” in which liver enzymes rise quickly and then fall quickly. He said the key safety considerations are rapid improvement within days and no bilirubin change, which he said Beam observed.

Bystander Editing and Protein Function Evans also addressed investor questions about bystander editing. He said BEAM-302 can create a mixture of corrected M protein and an M variant, a result Beam has known about and characterized over time.

Evans said Beam has shown that the variant is secreted normally, is functional and has a structure comparable to normal M protein. He also said the variant position is commonly varied in the human population and that the specific variant Beam creates is found in people and is not associated with disease.

He pointed to functional data showing direct inhibition of human neutrophil elastase using serum from treated patients, which he said demonstrated that the protein mixture created by the therapy is functional.

Regulatory Path and Liver Endpoints Evans said Beam has alignment with the FDA on an accelerated approval path for BEAM-302, describing it as a “classic accelerated approval” strategy rather than one reliant on newer regulatory mechanisms. He said the company is working with stable FDA review teams and that the agency’s main request was for 12 months of follow-up because alpha-1 levels can vary over time.

Evans said Beam plans to enroll 50 patients and follow them for one year before submitting the data. He said the biomarker package includes total alpha-1 levels, M protein levels, percentage of M protein, reduction in Z protein, protein functionality and inducibility.

On liver benefit, Evans said Beam believes BEAM-302 could help both lung and liver manifestations of alpha-1 antitrypsin deficiency by raising functional alpha-1 and lowering Z protein. He said Beam is conducting biopsies in Part B patients before treatment and at six and 12 months to assess whether aggregates resolve and whether fibrosis changes over time.

Evans said the Part B patients, who have more advanced liver disease, have so far tolerated the drug similarly to Part A patients, supporting an all-comer Cohort C.

Sickle Cell Program and Pricing Outlook Evans said Beam’s ex vivo sickle cell disease program, risto-cel, could have a BLA filing as early as the end of this year. He said Beam believes it has a strong manufacturing process, with a vein-to-vein time of just over four months, which he said could allow patients to be treated quickly and predictably.

Evans said risto-cel is aimed at severe sickle cell patients who may be candidates for a transplant-based option, while Beam also continues to work on in vivo approaches that could reach a broader sickle cell population over time.

On pricing, Evans said Beam would price a one-time alpha-1 therapy higher than one year of augmentation therapy, but said payers are sophisticated and evaluate long-term pharmacoeconomic value. He cited sickle cell disease as an example where high lifetime costs have supported genetic medicine pricing, while noting that it is too early to discuss specific pricing for alpha-1.

Evans said Beam believes alpha-1 antitrypsin deficiency has a strong value story because a one-time therapy could potentially address both lung and liver disease.

About Beam Therapeutics NASDAQ: BEAMBeam Therapeutics, Inc NASDAQ: BEAM is a biotechnology company dedicated to developing precision genetic medicines through its pioneering base editing platform. Headquartered in Cambridge, Massachusetts, with additional research facilities in Philadelphia, the company focuses on engineering molecular editors capable of making precise single-nucleotide changes in DNA. By harnessing its proprietary base editing technology, Beam aims to correct or disrupt disease-causing genetic variants at their source, offering the potential for novel therapies in areas with significant unmet medical need.

Founded in 2017 as a spin-out from Harvard University and the Broad and Whitehead Institutes, Beam was co-founded by leading academic researcher David R.

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 14:35 1mo ago
2026-05-25 13:37 2mo ago
Beam Therapeutics Inc. (BEAM) Presents at RBC Capital Markets Global Healthcare Conference 2026 Transcript
BEAM Beam Therapeutics
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Original source text
Beam Therapeutics Inc. (BEAM) Presents at RBC Capital Markets Global Healthcare Conference 2026 Transcript