Drug intelligence / Profile preview

SHR-A1811 + SHR-1316 + capecitabine

Development stage
Unknown
Lead developer
Jiangsu Hengrui Medicine
Modality
Small Molecules, Cytotoxic ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous, Oral
01

Overview

SHR-A1811 + SHR-1316 + capecitabine is an investigational combination therapy comprising two novel biologic agents and a standard chemotherapeutic. SHR-A1811 is an antibody-drug conjugate targeting Human epidermal growth factor receptor 2 (HER2), designed to deliver cytotoxic agents directly to HER2-expressing tumor cells, thereby enhancing antitumor efficacy while limiting systemic toxicity. It has demonstrated promising activity in advanced HER2-mutant non-small cell lung cancer and HER2-positive breast cancer[6][8]. SHR-1316, also known as adebrelimab, is a monoclonal antibody that targets Programmed death-ligand 1 (PD-L1), blocking its interaction with PD-1 and restoring T-cell mediated immune responses against tumors. It has shown efficacy in extensive-stage small cell lung cancer (ES-SCLC) and esophageal squamous cell carcinoma when combined with chemotherapy[3][4][5][7]. Capecitabine is an oral prodrug of 5-fluorouracil (5-FU), a widely used small molecule chemotherapeutic agent that inhibits thymidylate synthase, disrupting DNA synthesis in rapidly dividing cells.

Other names
Adebrelimab (for SHR-1316)
02

Targets

ERBB2 (Erb-b2 receptor tyrosine kinase 2)CD274 (Programmed cell death protein 1 ligand 1)TS (Thymidylate synthase)

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