FDA Expands Indication of Pfizer's Besponsa to Include Pediatric Patients with B-cell Precursor Acute Lymphoblastic Leukemia

FDA Expands Indication of Pfizer's Besponsa to Include Pediatric Patients with B-cell Precursor Acute Lymphoblastic Leukemia

Besponsa (inotuzumab ozogamicin) was initially approved in August 2017 for adults with relapsed or refractory CD22-positive B-cell precursor acute lymphoblastic leukemia.

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