BL 761309
BL 761309
U.S. License Holder:
Genentech Inc.
Date of License:
June-15-2023
Last Update:
Dec-15-2024
FDA-Approved IndicationsCOLUMVI (glofitamab-gxbm) is a bispecific CD20-directed CD3 T-cell engager indicated for the treatment of adult patients with relapsed or refractory diffuse large B-cell lymphoma, not otherwise specified (DLBCL, NOS) or large B-cell lymphoma (LBCL) arising from follicular lymphoma, after two or more lines of systemic therapy.
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