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4 March, 2026 |
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Our man in Miami, Max Bayer, talked yesterday with BIO's John Crowley, who runs the lobbying and trade group. Crowley isn't the only one trying to make sense of a changing FDA that, in the eyes of some biopharma leaders, feels harder to understand and less consistent — or at the very least, in a period of significant change. |
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Drew Armstrong |
Executive Editor, Endpoints News
@ArmstrongDrew
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by Max Bayer
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John Crowley, CEO of the trade group BIO, says he still supports FDA Commissioner Marty Makary even after a series of regulatory decisions on his watch have caused frustration and consternation among the biotech industry. In an interview with Endpoints News on Tuesday, Crowley said the FDA “needs to continue to succeed” and that
responsible regulatory risk is critical to fostering a healthy ecosystem for drug developers, particularly for rare disease treatments. He hasn’t seen as much of that. “Some of the decisions have been head-scratchers.” Crowley said. “We need some sharp review and focus, but the pattern here has been trouble in the rare diseases, particularly in cell and gene therapy.” | |
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by ENDPOINTS |
📉 Bayer workforce cuts continue: The German conglomerate reported 88,078 employees at the end of December, down from 88,500 as the third quarter concluded. When CEO Bill Anderson came aboard in 2023 and kickstarted a multiyear restructuring, the company had more than 100,000 staffers across its three divisions. Meanwhile, Bayer said it was discontinuing a Phase 1 Pompe disease AAV gene therapy, codenamed ACTUS-101, which was obtained from its 2020 AskBio buy. — Reynald Castaneda 🗞️ AnaptysBio's spinoff update: The biotech named its spinoff company First Tracks Biotherapeutics and will launch it in the second quarter. First Tracks will run AnaptysBio’s immunology portfolio, including its Phase 2 antibody rosnilimab for rheumatoid arthritis, as well as preclinical antibodies ANB033 and ANB101. AnaptysBio announced its spinoff plans in September. — Anna Brown |
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by Elizabeth Cairns
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Sanofi has paid $135 million upfront to license a potential therapy to tamp down transplant rejection from the Hong Kong-based company Sino Biopharmaceutical. The French pharma will get exclusive worldwide rights to develop, make and sell rovadicitinib, in a deal made via Sino’s subsidiary Chia Tai Tianqing Pharmaceutical. Sanofi is on the
hook for up to $1.4 billion in milestone payments, plus possible double-digit tiered royalties, according to a Wednesday securities filing. Sino described rovadicitinib as its “breakout star” in the field of rare diseases. It is a first-in-class inhibitor of both JAK, through which it exerts anti-inflammatory effects, and another enzyme called ROCK. ROCK blockade suppresses
overactivated T helper cells and boosts regulatory T cells, helping the patient achieve immune homeostasis. | |
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Jay Mei, Antengene CEO (Endpoints/PharmCube) |
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by Kyle LaHucik
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UCB is teaming up with Chinese biotech Antengene to develop a T cell engager in Amgen's arena, alongside bubbling competition from AstraZeneca, Merck and others. The Belgian pharma is stepping into the CD19xCD3 space in a pact with Antengene that features $60 million upfront and $20 million in near-term milestones. The biotech could collect another $1.1 billion across development, regulatory and sales milestones under the deal announced Tuesday evening. At the heart of the deal is ATG-201, which is part of Antengene's
sprawling pipeline of T cell engagers. Antengene will run Phase 1 trials of ATG‑201 and then hand over the development duties to UCB. The biotech said it will ask Chinese and Australian health regulators to approve the studies in the second quarter of this year. | |
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