BL 761040
BL 761040
U.S. License Holder:
Wyeth Pharms. Inc.
Date of License:
August-17-2017
Last Update:
May-23-2023
FDA-Approved IndicationsBESPONSA (inotuzumab ozogamicin) is a CD22-directed antibody-drug conjugate (ADC) indicated for the treatment of adults with relapsed or refractory B-cell precursor acute lymphoblastic leukemia (ALL).
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