Drug intelligence / Profile preview

vobramitamab tavatecan + pembrolizumab

Development stage
Phase 1
Lead developer
MacroGenics
Modality
Cytotoxic ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

MGC026 + pembrolizumab is an investigational combination regimen pairing vobramitamab tavatecan (MGC026), a B7-H3-directed antibody-drug conjugate (ADC), with pembrolizumab, an anti-PD-1 monoclonal antibody. Vobramitamab tavatecan consists of a humanized anti-B7-H3 monoclonal antibody (MGA017) site-specifically conjugated to a cleavable exatecan-based topoisomerase I (TOP1) inhibitor payload (SYNtecan E) with a drug-to-antibody ratio (DAR) of 4. Pembrolizumab is a well-established immune checkpoint inhibitor that blocks the interaction between PD-1 and its ligands, PD-L1 and PD-L2, thereby revitalizing T-cell-mediated antitumor immune responses. The combination is being developed by MacroGenics for the treatment of advanced solid tumors, with plans to initiate a Phase 1 expansion cohort in early 2027 for front-line patients with PD-L1-positive recurrent or metastatic squamous cell carcinoma of the head and neck (SCCHN).

Other names
MGC026 + KeytrudaMGC026 + pembrolizumabMGC026 and pembrolizumabMGC-026 and pembrolizumabMGC 026 and pembrolizumabMGC026/pembrolizumabvobramitamab tavatecan + Keytrudavobramitamab tavatecan and pembrolizumabvobramitamab tavatecan/pembrolizumab
02

Targets

B7-H3PDCD1 (Programmed cell death protein 1 receptor)

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