Drug intelligence / Profile preview

TQB2102 + benmelstobart + chemotherapy

Development stage
Unknown
Lead developer
Chia Tai-Tianqing Pharmaceutical Group
Modality
Small Molecules, Cytotoxic ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous, Oral
01

Overview

TQB2102 + benmelstobart + chemotherapy is a combination therapy regimen under development by Chia Tai Tianqing Pharmaceutical Group and Nanjing Shunxin Pharmaceutical Co., Ltd. for the treatment of HER2-positive gastroesophageal adenocarcinoma. TQB2102 is a biparatopic antibody-drug conjugate (ADC) that simultaneously targets two non-overlapping epitopes (ECD2 and ECD4) of the HER2 protein. It is linked to a topoisomerase I inhibitor payload via an enzyme-cleavable linker, designed to enhance HER2 internalization and signaling blockade. Benmelstobart (TQB2450) is a humanized IgG1 monoclonal antibody targeting PD-L1, which blocks the interaction of PD-L1 with PD-1 and CD80 receptors to restore anti-tumor immune responses. The chemotherapy component, typically capecitabine, provides additional cytotoxic activity. This combination is currently being evaluated in Phase II clinical trials to leverage the synergistic effects of HER2-targeted therapy, immune checkpoint inhibition, and traditional chemotherapy in patients with advanced or metastatic disease.

Other names
TQB2102 + TQB2450 + chemotherapyTQB2102 + benmelstobart + capecitabine
02

Targets

ERBB2 (Erb-b2 receptor tyrosine kinase 2)CD274 (Programmed cell death protein 1 ligand 1)TOP1 (DNA Topoisomerase I)

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