Sanofi and Cheplapharm announce mature medicines partnership
Sanofi plans to transfer 20 mature medicines and three manufacturing sites to Cheplapharm in exchange for a 26.4% equity stake in the German company.
SEC filing
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Sanofi plans to transfer 20 mature medicines and three manufacturing sites to Cheplapharm in exchange for a 26.4% equity stake in the German company.
SEC filing
The company confirmed the September 14 board appointment in a September 16 statement that included executive comments and details on Whitaker's background.
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The former FDA official and regulatory consultant joins as a Class II director effective September 15, 2026.
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The company appointed R. Duane Clark II and James Sapirstein to its board on September 8, 2026, as Ebstrocel nears potential commercialization.
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The combined company begins trading as KRSA on Nasdaq September 9, with cash expected to fund operations into 2029 as it advances its Alzheimer's antibody program.
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Cardiovascular gene-editing company reports first clinical data expected in H1 2027 and cash runway into H1 2029 after $155.5 million IPO and Sanofi private placement.
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The company announced a call and webcast on August 14, 2026 featuring its CEO, COO, CFO, and IR head.
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The company grew its board to nine seats and named Reed, who oversees Johnson & Johnson's innovative medicine research and development, to a Class II director term.
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Belgium-based Agomab Therapeutics plans to add the two as non-executive directors, pending a shareholder vote in September 2026.
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The European Commission extended MenQuadfi's indication to cover infants as young as six weeks against invasive meningococcal disease, expanding on the prior 12-months-and-older approval.
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Novavax lifted its full-year revenue framework to $235-$275 million and said Sanofi is in advanced regulatory talks over its combination COVID-flu trial timing.
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Second-quarter update details 88% viral suppression in hepatitis delta trial, Astellas collaboration progress, and $1.0 billion cash position.
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Faster-than-planned enrollment in the STAT6 degrader's Phase 2b trial pulls the readout forward to year-end 2026 and sets up an earlier Phase 3 start.
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Regeneron's second-quarter release recaps June 2026 FDA and EMA acceptance of cemdisiran filings for generalized myasthenia gravis and a Phase 3 fianlimab trial that missed its primary endpoint.
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Teva reported a $576 million net loss tied to the Emalex acquisition and ecopipam NDA filing, while raising its 2026 revenue outlook for AUSTEDO, AJOVY and UZEDY.
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The clinical-stage CRISPR company will sell 8,580,000 shares on Nasdaq under "SCTX," with a Sanofi affiliate committing to a concurrent private placement.
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The company's chief medical officer will speak on changing treatments in bladder cancer at the BTIG Virtual Biotechnology Conference on July 28, 2026.
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Paulo Fontoura steps down from Lakefront Biotherapeutics' board following his appointment to a top research role at Sanofi.
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