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What Coherus' $40M sale of its Humira biosimilar says about the crowded market

Coherus BioSciences is selling its Humira biosimilar for just $40 million, only three years after it won FDA approval, showing just how crowded the market has become for Humira and its nine biosimilar...

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House panel advances bill to allow Medicare to cover obesity drugs

The House Ways and Means Committee on Thursday cleared a bill that would direct Medicare to cover obesity treatments — but only for a small sliver of beneficiaries. The committee voted 36-4 to pass an...

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Lykos takes another hit as ICER lays out 'insufficient' evidence for...

A key independent drug pricing organization has concluded that the available evidence for Lykos Therapeutics’ MDMA-assisted psychotherapy is “insufficient” and it can’t be compared to other...

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Immunology biotech Alumis secures $250M in shrunken IPO

Alumis, an immunology drug developer on the cusp of Phase 3, will go public Friday in a smaller IPO than it originally projected. The Bay Area startup sold 13.12 million shares $ALMS at $16 apiece to...

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Autoimmune brain disease startup Arialys gets new leader; Intellia, Arvinas...

Peter Flynn Peter Flynn has taken the helm from Avalon BioVentures managing partner Jay Lichter at Arialys Therapeutics, a startup that is developing treatments in the field of immunoneuropsychiatry —...

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FDA rejects Rocket Pharma’s ultra-rare immune disease gene therapy over...

The FDA rejected Rocket Pharmaceuticals’ gene therapy for leukocyte adhesion deficiency-I (LAD-I), requesting “limited additional” manufacturing information. The company announced the rejection on...

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Savara’s $100M offering; New biotech to test Eisai drug in Ph2

Plus, news about Daiichi Sankyo, Seagen, Lantheus, Life Molecular Imaging, Astellas Gene Therapies, Eli Lilly and Aparito: Savara prices $100M offering: The Langhorne, PA-based biotech will secure...

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J&J details Phase 3 success of autoimmune disease drug, touting broader range...

Johnson & Johnson’s experimental autoimmune treatment lowered the impact of myasthenia gravis on daily life compared to placebo in antibody-positive patients in a late-stage study. The drug is part...

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Rovi teases acquisition offers for its CDMO unit potentially worth €2B to €3B

Rovi has attracted multiple buyout bids for its contract manufacturing business after the company said it was weighing its options for the division several months ago. The Spanish drugmaker said...

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Inside BARDA's multibillion-dollar effort to fund long-shot biotechs for Covid

In 2023, Vaxart halted work on its oral vaccine for Covid-19, and didn’t even have enough money to finish 2024. Now, the US government is lending a big hand. The Biomedical Advanced Research and...

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Why the Supreme Court's overrule of Chevron has major implications for the FDA

The Supreme Court on Friday overruled a longstanding legal doctrine that gives federal agencies latitude to interpret federal law, which legal scholars and industry have warned could destabilize the...

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CMS spells out how states can join new cell and gene therapy access pilot

The Centers for Medicare and Medicaid Services plans to begin testing whether outcomes-based agreements might improve access to two new gene therapies approved for sickle cell disease. Cell and gene...

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Federal grand jury indicts Cassava collaborator for allegedly defrauding NIH

A Maryland federal grand jury on Thursday indicted neuroscientist Hoau-Yan Wang, a longtime Cassava Sciences collaborator, for allegedly defrauding the NIH out of about $16 million in federal grant...

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Merck calls ACIP's pneumococcal recommendation a 'missed opportunity,'...

The CDC’s Advisory Committee on Immunization Practices (ACIP) has recommended Merck’s recently approved 21-valent pneumococcal vaccine Capvaxive for adults 65 years and older, and for certain younger...

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EMA's CHMP recommends 10 new drugs as Pierre Fabre overactive bladder med...

Pierre Fabre’s overactive bladder medication won approval in Europe on Friday as a panel of experts at the European Medicines Agency separately recommended 10 others for first-time nods. The approval...

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Alnylam's big Phase 3 win; LGBTQ+ leaders charting paths; Chevron overturned;...

Welcome back to Endpoints Weekly, your review of the week’s top biopharma headlines. Want this in your inbox every Saturday morning? Current Endpoints readers can visit their reader profile to add...

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Artiva refiles for IPO three years after original plans in a vastly different...

Artiva Biotherapeutics, a clinical-stage NK cell therapy biotech, is trying again for the public markets, it revealed Friday afternoon in an SEC filing. The San Diego biotech is going for a Nasdaq...

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#EAN24: Dianthus teases preclinical data for autoimmune drug as it starts...

Dianthus Therapeutics has unveiled in vitro results of its drug candidate in a pair of autoimmune disease models, supporting recent efforts to start mid-stage studies. The first data set from the blood...

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Eisai takes over development of ADC after Bristol Myers ends $650M collaboration

Due to Bristol Myers Squibb’s portfolio prioritization efforts, Eisai is taking back an antibody-drug conjugate that they originally teamed up on in 2021. Eisai will now develop and commercialize the...

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Aerovate plans to lay off nearly all employees after trial failure

Aerovate Therapeutics plans to lay off nearly all its employees two weeks after its lead asset flunked a mid-stage trial. The company disclosed the workforce reduction on Friday evening in an SEC...

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