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Considering the significant unmet need for those with pancreatic cancer, the European Medicines Agency said yesterday it will speed up its review of Revolution Medicines' pan-RAS inhibitor daraxonrasib, which has been hailed as a breakthrough after doubling survival times in a Phase 3 trial when it was compared with chemo. The EMA said the sped-up review for daraxonrasib, which also will see an expedited review in the US thanks to the FDA's Commissioner's National Priority Voucher program, "will serve as an example for some of the provisions of the reformed EU pharmaceutical legislation which is expected to strengthen the use of phased reviews." Stay tuned for more. |
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Zachary Brennan |
Senior Editor, Endpoints News
@ZacharyBrennan
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Photo by Annabelle Gordon/Sipa USA via AP Images |
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by Zachary Brennan
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The Trump administration is pushing the FDA to cement the details behind its proactive public release of rejection letters sent to pharma companies. The rulemaking... | |
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by Zachary Brennan
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There's an answer emerging on the multibillion-dollar question of whether the Trump administration's gutting of FDA staff in April 2025 would slow down drug approvals... | |
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by Max Bayer
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Acting FDA CDER director Michael Davis has promoted a longtime FDA staffer as an acting deputy director at the drug center. Lisa Yanoff, an agency... | |
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by Nicole DeFeudis
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A proposed rule would cut the rates by which Medicare pays hospitals for 340B drugs by more than a third, reviving a similar policy introduced... | |
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by Zachary Brennan
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An FDA warning letter sent late last month to Genzyme's Ireland-based manufacturing site, now owned by Sanofi, raises significant quality- and data-related issues. On data... | |
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Nate Fernhoff, Orca Bio CEO |
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by Lei Lei Wu
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The FDA gave the go-ahead to Orca Bio’s T cell therapy that would reduce transplant-related complications for blood cancer patients. The therapy will be branded... | |
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