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Just 16 months after Johnson & Johnson scored its initial FDA app | Sixteen months after Johnson & Johnson scored its initial FDA approval for Imaavy, the pharma giant has tacked on a label expansion for the monoclonal antibody. The U.S. regulator has signed off on Imaavy to treat warm autoimmune hemolytic anemia, a rare disorder which destroys red blood cells.
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J&J’s Imaavy wins label expansion; Two approvals in Japan

Johnson & Johnson Secures FDA Approval For First Rare Anemia Treatment - Johnson & Johnson (NYSE:JNJ)

FDA approves IMAAVY® (nipocalimab-aahu) as first-ever treatment for warm autoimmune hemolytic anemia (wAIHA), representing a landmark advancement for patients

First Drug OK'd for Warm Autoimmune Hemolytic Anemia