FDA: Post-Approval Trial Of Fast-Tracked Myeloma Drug Shows Increased Death Risk

Mealey's (August 3, 2021, 3:10 PM EDT) -- SILVER SPRING, Md. — The Food and Drug Administration on July 28 told patients and health care professionals that post-approval clinical trial results show an increased risk of death associated with Pepaxto brand melphalan flufenamide, a drug approved in February under an accelerated approval process, to treat patients with multiple myeloma....

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