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24 July, 2026 |
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We're on Day 2 of a marathon peptide advisory committee meeting. Shelby Livingston has been keeping track of the arguments presented, how the votes broke down, and what's ahead based on the recommendations of the group. Read the full coverage here. |
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Lydia Ramsey Pflanzer |
Deputy Editor, Endpoints News
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by Nicole DeFeudis
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Amgen shared a new analysis with the FDA that the company said supports keeping its controversial rare disease drug Tavneos on the market. The submission... | |
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by Shelby Livingston
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An FDA advisory committee voted to recommend expanding access to popular peptides used by health and wellness enthusiasts for repairing muscles, healing injuries, boosting metabolism... | |
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by Anna Brown
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Minoryx Therapeutics finally scored backing from EU regulators for its neurological drug that’s faced multiple hurdles. Meanwhile, Zevra’s rare disease drug got a setback in... | |
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by ENDPOINTS |
Plus news about Abbvie and Genmab, Johnson & Johnson and Mannkind. Novo urges court to block Lilly’s GLP-1 ads: Novo Nordisk asked a New Jersey... | |
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by Elizabeth Cairns
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Sanofi has decided to stop working on a drug for eczema it had hoped would be a successor to its immunological megablockbuster Dupixent. The French... | |
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