Ensysce Biosciences Phase 2 Protocol for CY200 - A Neuroplastigen for the Treatment of CRPS - Submitted to the UK MHRA
Ensysce Biosciences announced it submitted the protocol (CYBIO_001) for a Phase 2a clinical study of CY200 to the UK Medicines and Healthcare products Regulatory Agency (MHRA). The randomised, double-blind, placebo-controlled proof-of-concept study is designed to evaluate CY200's efficacy, safety, and tolerability in adults with Complex Regional Pain Syndrome Type 1.
Why it matters — This submission marks a key regulatory step toward initiating the first Phase 2 study of the newly acquired CY200 candidate, advancing Ensysce's CRPS-focused neuroplastogenic pipeline.