NoticiasVisión general del mercadoGSK dice que la FDA extiende el período de revisión para el fármaco experimental momelotinib

GSK dice que la FDA extiende el período de revisión para el fármaco experimental momelotinib

(Reuters) – British drugmaker GSK Plc on Friday said the U.S. Food and Drug Administration has extended the review period for its experimental drug momelotinib, which is designed to treat anaemic patients with a type of bone marrow cancer called myelofibrosis.

Momelotinib is not currently approved in any market.

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