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FDA proposes to withdraw Amgen's rare autoimmune disease drug

FDA proposes to withdraw Amgen's rare autoimmune disease drug

ReutersTue, April 28, 2026 at 1:04 AM UTC

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The Amgen logo is seen in this illustration taken August 3, 2025. REUTERS/Dado Ruvic/Illustration

April 27 (Reuters) - The U.S. Food and Drug ‌Administration's Center for Drug ‌Evaluation and Research on Monday ​proposed withdrawing approval of Amgen's drug for a group of rare autoimmune diseases, ‌citing ⁠a lack of proven effectiveness and untrue ⁠statements in the application that led to its ​approval.

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In March, ​the ​FDA said it ‌identified 76 cases of drug-induced liver injury with evidence suggesting a causal link to Tavneos, including seven ‌cases of ​vanishing bile duct ​syndrome (VBDS), ​a rare condition ‌that can cause permanent ​liver ​damage. Eight deaths were reported among those cases.

(Reporting ​by ‌Natalia Bueno Rebolledo in ​Mexico City; Editing by ​Rashmi Aich)

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