Drug intelligence / Profile preview

becotatug vedotin + zimberelimab

Development stage
Unknown
Lead developer
Lepu Biopharma
Modality
Cytotoxic ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

Becotatug vedotin + zimberelimab is an investigational combination therapy comprising an epidermal growth factor receptor (EGFR)-targeted antibody-drug conjugate (ADC) and a programmed cell death protein 1 (PD-1) inhibitor. Becotatug vedotin (MRG003) consists of a humanized anti-EGFR monoclonal antibody conjugated to the potent microtubule-disrupting agent monomethyl auristatin E (MMAE) via a protease-cleavable valine-citrulline linker. Upon binding to EGFR on the surface of cancer cells, the ADC is internalized, releasing MMAE to induce cell cycle arrest and apoptosis. Zimberelimab is a fully human monoclonal antibody that targets PD-1, preventing its interaction with PD-L1 and PD-L2 to restore and enhance T-cell-mediated anti-tumor immune responses. This combination is being evaluated for its potential synergistic efficacy in treating recurrent or metastatic squamous cell carcinomas of the cervix, vulva, and vagina, particularly in patients who have failed prior standard-of-care therapies.

Other names
MRG003 + zimberelimabMRG003 + GLS-010
02

Targets

PDCD1 (Programmed cell death protein 1 receptor)EGFR T790M (Epidermal growth factor receptor T790M mutant)

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