Drug intelligence / Profile preview

RCI002

Development stage
Preclinical
Lead developer
Rudacure
Modality
Small Molecules
Administration
Intraperitoneal
01

Overview

RCI002 is a small molecule drug candidate developed by Rudacure for the treatment of various chronic pain conditions, including complex regional pain syndrome (CRPS), osteoarthritis, and neuropathic pain. It employs a unique biased dual-targeting mechanism, acting as a potent and selective TRPV1 antagonist and a biased ligand of the mu-opioid receptor (MOR). Unlike traditional TRPV1 antagonists that often cause hyperthermia by blocking all modes of channel activation, RCI002 specifically inhibits capsaicin-induced activation while sparing pH and heat-induced activation, potentially improving its safety profile. Preclinical studies have demonstrated its efficacy in reducing hypersensitivity in models of chemotherapy-induced peripheral neuropathy (CIPN), showing superiority to pregabalin. The drug is currently in IND-enabling development.

02

Targets

TRPV1 (Transient receptor potential cation channel subfamily V member 1)

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