Pharma: Page


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    Regeneron makes obesity push; Atai, Alto ink brain drug deals

    Regeneron licensed a weight loss drug and revealed study data for a pair of muscle-preserving medicines. Elsewhere, two neuroscience biotechs cut deals and Bluebird officially went private.

    By BioPharma Dive staff • June 4, 2025
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    Merck, Daiichi pull approval application for ADC in lung cancer

    A therapy at the center of their $22 billion alliance failed to extend survival in a type of lung tumor, leading the companies to abandon a U.S. submission.

    By May 29, 2025
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    Trendline

    Top 5 stories from BioPharma Dive

    Looming patent expiries this decade and intensifying competition from China are forcing drugmakers to adapt, while new opportunities open up in oncology and in neuroscience.

    By BioPharma Dive staff
  • Behind the Breakthroughs: How Almac Powers Clinical Trial Success With Care – A partnership with BioPharma Dive, highlighting Almac’s commitment to patient-centric clinical trial support.
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    Sponsored by Almac Clinical Services

    [Podcast] Behind the Breakthroughs: How Almac Powers Clinical Trial Success with Care

    Agile biopharma firms are driving breakthroughs. Learn how they ensure clinical trial success in this podcast.

    By BioPharma Dive's studioID • May 28, 2025
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    Biogen strikes RNAi deal with City; Aurion withdraws IPO

    City will receive $46 million from Biogen under the alliance. Elsewhere, Angelini Pharma licensed a rare disease therapy and the FDA refused to review a Savara lung drug.

    By BioPharma Dive staff • May 27, 2025
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    ASCO / Nick Agro

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    ASCO25

    Zepzelca, Tecentriq combo extends survival in hard-to-treat lung cancer

    Still, the therapies’ modest benefit as a maintenance therapy points to how better treatments are needed for small cell lung cancer, according to one physician.

    By May 22, 2025
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    FDA advisers pan Pfizer’s PARP drug; Sarepta to resume Duchenne study

    An eight-member panel voted unanimously against wider use of Pfizer’s Talzenna in advanced prostate cancer. Elsewhere, U.K. regulators cleared Sarepta to restart an Elevidys study and Altos Labs bought a startup.

    By BioPharma Dive staff • May 22, 2025
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    FDA panel backs Darzalex for early stage multiple myeloma

    Agency drug reviewers had questioned patient risk criteria and the efficacy endpoint used in a key trial supporting J&J's drug.

    By May 21, 2025
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    Tourmaline shares fall on Phase 2 data; Schrödinger cuts staff

    Tourmaline Bio disclosed results for a potential rival to a Novo Nordisk drug. Elsewhere, data emerged for a psychedelic and CRISPR Therapeutics expanded its toolkit.

    By BioPharma Dive staff • May 20, 2025
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    China competition

    Pfizer buys into PD-1/VEGF competition with 3SBio deal

    Pfizer will pay China’s 3SBio $1.25 billion up front to access a cancer drug that could rival Akeso and Summit’s closely watched immunotherapy ivonescimab.

    By May 20, 2025
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    Permission granted by PHIL
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    Sponsored by PHIL

    Bridging the data gaps that impact retail and specialty-lite success

    Learn how to leverage predictive analytics and measure top KPIs to maximize patient outcomes, provider engagement and brand performance on this webinar from PHIL and Syneos Health.

    May 19, 2025
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    Regeneron defeats Amgen in PCSK9 case; 2 cell therapy biotechs cut staff

    A federal jury found Amgen liable for violating antitrust and tort laws. Elsewhere, Allogene and Kyverna trimmed staff and the FDA scheduled an advisory meeting.

    By May 16, 2025
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    Novo CEO to depart as obesity drugmaker’s challenges rise

    Lars Fruergaard Jørgensen will step down after eight years helming the Danish drugmaker, shares of which have shed half their value in the past 12 months.

    By Ned Pagliarulo • Updated May 16, 2025
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    Pharma reshoring

    Sanofi to pour more than $20B into US drug research and manufacturing

    The French drugmaker joined several peers in promising new investments in U.S. drug production, but cautioned plans could change amid shifting Trump administration policies.

    By Kristin Jensen • May 15, 2025
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    Stopping a ‘moral obscenity’: Senate Judiciary Committee expresses support for PBM reform

    Sen. Chuck Grassley, R-Iowa, suggested Congress could once again move to overhaul PBMs’ controversial business practices after legislators pass President Donald Trump’s conservative megabill this summer.

    By Rebecca Pifer Parduhn • May 15, 2025
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    Trump revives ‘most favored nation’ plan in effort to cut US drug prices

    The proposal would see the HHS set price targets other countries pay for certain medicines, kicking off a round of discussions with substantial ramifications for drugmakers. It’s likely to be challenged in court, however.

    By , Ned Pagliarulo • Updated May 12, 2025
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    Eli Lilly extends Purdue alliance; EMA investigates Valneva shot

    The big pharma will spend up to $250 million over the next eight years of the collaboration. Elsewhere, CRISPR Therapeutics unveiled new data and Vivo Capital raised funds.

    By BioPharma Dive staff • May 9, 2025
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    Pharma reshoring

    Gilead, bracing for tariffs, joins peers in US drug production push

    The company added to a recent flurry of pledges by pharmaceutical companies, promising $11 billion in new capital and operational investments in U.S. drug manufacturing.

    By Kristin Jensen • May 8, 2025
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    Courtesy of Novo Nordisk
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    Obesity drugs

    Novo cuts forecasts as compounded GLP-1s weigh on sales

    The maker of Ozempic and Wegovy expects lower sales and profit growth this year despite recent victories against compounders.

    By Ned Pagliarulo • May 7, 2025
  • U.S. President Donald Trump, accompanied by Food and Drug Administration Commissioner Marty Makary (L), National Institutes of Health Director Jayanta Bhattacharya (2nd-L), Health and Human Services Secretary Robert F. Kennedy Jr. (2nd-R) and Domestic Policy Council Director Vince Haley (R), signs an executive order in the Oval Office at the White House on May 05, 2025 in Washington, DC
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    Trump orders FDA to help speed building of new drug factories

    Yet regulatory relief for U.S. expansion could be accompanied by new tariffs and drug pricing rules.

    By May 6, 2025
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    Bluebird pleads for deal support; Unity, Mersana lay off staff

    Bluebird urged shareholders to back a take-private deal that could close imminently. Elsewhere, Unity Biotechnology began a strategic review and Mersana announced plans to cut more than half its workforce.

    By BioPharma Dive staff • May 6, 2025
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    Amgen’s Stelara biosimilar gets off to fast start

    Sales of the company’s copycat to J&J’s blockbuster reached $150 million in the first quarter, adding to a surge in revenue for Amgen's biosimilar business.

    By May 2, 2025
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    Pharma reshoring

    Pharma downplays tariff threat, even as risks remain unclear

    Drugmaker executives have projected confidence they can mitigate the impact of any levies Trump imposes on the industry. Yet they're adjusting inventory and production nonetheless.

    By Ned Pagliarulo , May 1, 2025
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    CVS strikes Wegovy deal with Novo Nordisk

    The deal could expand access to its in-demand obesity drug at the expense of Eli Lilly, whose shares fell by double digits on Thursday.

    By Rebecca Pifer Parduhn • May 1, 2025
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    AstraZeneca quietly exits neuroscience

    The company removed experimental drugs for Alzheimer’s, migraine and pain from its pipeline to focus more resources on “core therapeutic areas” and “high value” programs.

    By May 1, 2025
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    J&J secures FDA OK for immune drug touted as future blockbuster

    The company has predicted that Imaavy — now approved for myasthenia gravis — could eventually earn more than $5 billion in annual sales at its peak.

    By Ned Pagliarulo • April 30, 2025