PREVENTION OF NEUROPATHIC PAIN WITH EXPECTED REDUCED SIDE-EFFECT.
Chemotherapy-induced peripheral neuropathic pain is a major public health problem because available treatments produce incomplete relief, and have dose limiting side effects.
Our research team has developed a new asset that consists in :
1 | Repurposing of Riluzole, a non-selective TREK1 activator with known neuroprotective action initially prescribed in amyotrophic lateral sclerosis (ALS) as a solution to prevent and cure neuropathic pain induced by neurotoxic chemotherapies.
2 | Reduction of associated comorbidities
Competitive Advantages
● Response to unmet therapeutic need
● Attractive to speed up drug development
● Contribute to Health-Related Quality of Life improvement
● Non-opioid preventive pain relief
Development Status
● In vivo POC in oxaliplatin, taxane and vinca-alkalo.ds induced neuropathic mouse and rat models. Also, Riluzole didn’t affect the anticancer effect of oxaliplatinin the mouse model of colorectal cancer (ApcMin)
● Validation of a MoA based on TREK1 channel activation and inhibition of synaptic glutamate release without affecting the antineoplasic properties
● Ongoing Clinical Phase II, multicenter, randomized, double-blind, placebo-controlled clinical trial on 210 patients with stage II/III colorectal cancer