Ensysce Biosciences Inc., a clinical-stage pharmaceutical company, has announced the full enrollment of Part 2 of the PF614-MPAR-102 clinical study. This phase of the study aims to examine the effect of food on the company's MPAR technology, which is designed to enhance opioid safety. The PF614-MPAR, which has been awarded the FDA's Breakthrough Therapy designation, incorporates Ensysce's proprietary TAAP™ and MPAR® technologies to provide overdose protection while maintaining pain relief efficacy. The study is supported by a three-year grant from the National Institute on Drug Abuse, with funding secured through May 2027. Results of this clinical trial have not yet been presented.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Ensysce Biosciences Inc. published the original content used to generate this news brief via ACCESS Newswire (Ref. ID: 1042177) on June 24, 2025, and is solely responsible for the information contained therein.
Comments