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Wednesday, August 14, 2024

FDA Approves Incyte's (INCY) Niktimvo for cGVHD

 On August 14, 2024, the Food and Drug Administration approved axatilimab-csfr (Niktimvo, Incyte Corporation), a colony stimulating factor-1 receptor-blocking antibody, for the treatment of chronic graft-versus-host disease (cGVHD) after failure of at least two prior lines of systemic therapy in adult and pediatric patients weighing at least 40 kg.

https://www.streetinsider.com/Corporate+News/FDA+Approves+Incytes+%28INCY%29+Niktimvo+for+cGVHD/23601071.html

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