Drug intelligence / Profile preview

sacituzumab govitecan + tislelizumab

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

Overview

This drug combination consists of sacituzumab govitecan (Trodelvy) and tislelizumab (Tevimbra). Sacituzumab govitecan is a trophoblast cell-surface antigen 2 (Trop-2)-directed antibody-drug conjugate (ADC) that utilizes a hydrolyzable linker to deliver SN-38, a potent topoisomerase I inhibitor, directly to cancer cells. Tislelizumab is a humanized IgG4 monoclonal antibody designed to bind to the programmed cell death protein 1 (PD-1) receptor, thereby blocking its interaction with PD-L1 and PD-L2 to restore T-cell mediated anti-tumor immune responses. The combination is being investigated in the TREND-02 trial, sponsored by the First Hospital of China Medical University, as a neoadjuvant therapy for early-stage triple-negative breast cancer (TNBC). The rationale for the combination is based on the potential for the ADC to induce immunogenic cell death, which may synergize with the checkpoint inhibition provided by tislelizumab.

Brand names
Trodelvy + Tevimbra
Other names
sacituzumab govitecan plus tislelizumabSG plus tislelizumab
02

Targets

PDCD1 (Programmed cell death protein 1 receptor)TACSTD2 (Tumor-associated calcium signal transducer 2)TOP1 (DNA Topoisomerase I)

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