Drug intelligence / Profile preview

ZYSM005

Development stage
Preclinical
Lead developer
Yantai Rongchang Pharmaceutical
Modality
Small Molecules
Administration
Oral
01

Overview

ZYSM005 is a small molecule inhibitor developed by Yantai Rongchang Pharmaceutical that specifically targets the active (ON-state) of the KRAS G12D mutant protein. KRAS G12D is a common oncogenic driver mutation found in a variety of solid tumors, most notably in pancreatic, colorectal, and lung cancers. Unlike many first-generation KRAS inhibitors that bind to the inactive (OFF-state) of the protein, ZYSM005 is designed to bind to the GTP-bound active form, potentially providing more direct and potent inhibition of downstream signaling pathways. The program is currently in the lead optimization and preclinical candidate (PCC) selection stage for the treatment of advanced solid tumors.

02

Targets

KRASG12D (Kirsten rat sarcoma viral oncogene homolog (KRAS) G12D mutant)

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