FDA Extends Review Period for Selinexor in Myeloma
March 15, 2019 - The FDA has added 3 months to the review period for a new drug application (NDA) for selinexor for the treatment of patients with penta-refractory multiple myeloma, making the new action date July 6, 2019. Karyopharm Therapeutics, Inc, the manufacturer of ...Leggi tutto