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FDA approves Niktimvo for chronic graft-versus-host disease, a first for this condition.
The FDA has approved Niktimvo (axatilimab-csfr) in 9 mg and 22 mg vial sizes, developed by Incyte and Syndax Pharmaceuticals, as the first treatment for chronic graft-versus-host disease (GVHD).
It targets CSF-1R to reduce inflammation and fibrosis.
Approved for adults and pediatric patients over 40 kg who have tried at least two other treatments, Niktimvo will be available for order in early February.
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La FDA aprueba Niktimvo para la enfermedad de injerto contra huésped crónica, una primera para esta afección.