Drug intelligence / Profile preview

CRB-701

Development stage
Phase 3
Lead developer
Corbus Pharmaceuticals
Modality
Small Molecules, Cytotoxic ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

CRB-701 (SYS6002) is a next-generation antibody-drug conjugate (ADC) designed to target Nectin-4, a clinically validated tumor-associated antigen highly expressed in several solid tumors, including urothelial and cervical cancers. The drug consists of a novel anti-Nectin-4 monoclonal antibody linked via a site-specific, cleavable linker to the cytotoxic payload monomethyl auristatin E (MMAE), with a homogenous drug-antibody ratio of 2. This third-generation linker technology aims to reduce dose-limiting toxicities seen with earlier ADCs such as enfortumab vedotin by enabling more stable systemic circulation and efficient intra-tumoral drug release. CRB-701 is being developed primarily for advanced solid tumors expressing high levels of Nectin-4, including metastatic urothelial carcinoma and relapsed/refractory metastatic cervical cancer. It has received FDA fast track designation for relapsed/refractory metastatic cervical cancer and is currently under investigation in Phase 1/2 clinical trials in the US, UK, and China[1][3][5][6].

Other names
SYS6002SYS-6002SYS 6002CRB-701CRB701CRB 701
02

Targets

PVRL4 (Nectin cell adhesion molecule 4)TUBB (Tubulin (alpha and beta subunits))

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