Drug intelligence / Profile preview

blinatumomab + glofitamab + teclistamab + talquetamab + epcoritamab + elranatamab

Development stage
Unknown
Lead developer
Amgen
Modality
Bispecific Antibodies → Multispecific Antibodies → Engineered Antibody Formats → Antibody-Based Therapeutics
Administration
Intravenous, Subcutaneous
01

Overview

**Blinatumomab + glofitamab + teclistamab + talquetamab + epcoritamab + elranatamab** is a hypothetical combination regimen of six bispecific T-cell engager antibodies targeting B-cell antigens for potential use in hematologic malignancies. Blinatumomab (BiTE®, CD19/CD3) is FDA-approved for CD19-positive B-cell precursor acute lymphoblastic leukemia (B-ALL) across multiple lines including consolidation. The others—glofitamab (CD20/CD3), teclistamab and elranatamab (BCMA/CD3), epcoritamab (CD20/CD3), talquetamab (GPRC5D)—are approved or in late development primarily for relapsed/refractory multiple myeloma (RRMM) or non-Hodgkin lymphoma (NHL). This multi-TCE mix aims to engage T cells against diverse tumor antigens (CD19, CD20, BCMA, GPRC5D) to overcome resistance via antigen loss, though no clinical trials or approvals exist for this exact combination, posing risks of overlapping cytokine release syndrome, neurotoxicity, and B-cell aplasia.

02

Targets

CD19 (B lymphocyte antigen CD19)CD20 (B-lymphocyte antigen CD20)CD3 (T-cell surface glycoprotein CD3)BCMA (B-cell maturation antigen)

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