Drug intelligence / Profile preview

SHR-A2102 + disitamab vedotin

Development stage
Unknown
Lead developer
Hengrui Pharmaceutical
Modality
Cytotoxic ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

SHR-A2102 + disitamab vedotin is an investigational combination therapy comprising two distinct antibody-drug conjugates (ADCs) targeting Nectin-4 and HER2, respectively. SHR-A2102, developed by Hengrui Pharmaceutical, consists of a humanized IgG1 monoclonal antibody against Nectin-4 conjugated to a topoisomerase I inhibitor payload via a cleavable linker. Disitamab vedotin (RC48), developed by RemeGen, is a HER2-directed ADC featuring a humanized antibody conjugated to the microtubule-disrupting agent monomethyl auristatin E (MMAE). The combination is designed to provide synergistic anti-tumor activity by targeting two different cell-surface antigens frequently co-expressed in solid tumors and delivering two distinct cytotoxic payloads. It is currently being evaluated in a Phase 1b/2 clinical trial (NCT06417554) for patients with advanced solid tumors, including urothelial carcinoma, non-small cell lung cancer, and esophageal cancer.

Other names
SHR-A2102 + RC48
02

Targets

TOP1 (DNA Topoisomerase I)TUBB (Tubulin (alpha and beta subunits))PVRL4 (Nectin cell adhesion molecule 4)ERBB2 (Erb-b2 receptor tyrosine kinase 2)

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