Drug intelligence / Profile preview

SHCW-8602

Development stage
Phase 1
Lead developer
Kunming Yuanrui Pharmaceutical
Modality
Small Molecules
Administration
Oral
01

Overview

SHCW-8602 (also known as SP-C01) is an orally bioavailable, small-molecule dual modulator that acts as a soluble epoxide hydrolase (sEH) inhibitor and a peroxisome proliferator-activated receptor gamma (PPARγ) partial agonist. Developed by Guangdong Hongshanhu Pharmaceutical (also known as Guangdong Red Coral Pharmaceutical) in collaboration with Shenyang Pharmaceutical University and Kunming Yuanrui Pharmaceutical, SHCW-8602 is designed to treat inflammatory and neuropathic pain. By simultaneously inhibiting sEH (which prevents the degradation of anti-inflammatory epoxyeicosatrienoic acids) and partially activating PPARγ, the drug exerts synergistic anti-inflammatory and analgesic effects while potentially mitigating the side effects typically associated with full PPARγ agonists, such as fluid retention and weight gain. SHCW-8602 is currently in Phase 1 clinical development for the treatment of pain.

02

Targets

EPHX2 (Soluble epoxide hydrolase)PPARG (Peroxisome proliferator-activated receptor gamma)

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