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"The FDA has approved the supplemental biologics license application for blinatumomab (Blincyto, Amgen) to include new data supporting the treatment of pediatric patients with Philadelphia chromosome-negative (Ph–) relapsed or refractory B-cell precursor acute lymphoblastic leukemia (ALL). This indication is approved under accelerated approval, and continued approval may be contingent upon verification of clinical benefit in subsequent trials.", www.ptcommunity.com
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