Ensysce describes PF614-MPAR's automatic overdose protection.
The opioid reduces exposure above therapeutic thresholds, holds FDA Breakthrough Therapy designation, and addresses 80,000 annual U.S. overdose deaths with NIDA support.
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Biotech company developing abuse-deterrent opioid therapies
ensysce.comLast updated
In short: Ensysce advanced its clinical-stage overdose-protection opioid programs while securing federal funding and addressing compliance issues.
The opioid reduces exposure above therapeutic thresholds, holds FDA Breakthrough Therapy designation, and addresses 80,000 annual U.S. overdose deaths with NIDA support.
The FDA recognized it as a substantial improvement over existing therapies for oral overdose protection. Ensysce has enrolled the first patient in Part 3 of the PF614-MPAR-102 study.
It is the only opioid to receive this designation for oral overdose protection, with MPAR technology built into the molecule. Ensysce is working to bring it to clinical reality.
Part 3 of PF614-MPAR-102 is the last stage, building on prior reduced opioid exposure results and moving closer to a complete dataset for MPAR overdose-protection.
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Funds Advance FDA-Designated Breakthrough Therapy First-in-Class Opioid with Oral Overdose-Protection · SAN DIEGO, CA / ACCESS Newswire / July 14, 2026 / Ensysce Biosciences, Inc.
Detailed price information for Ensysce Biosciences Inc (ENSC-Q) from The Globe and Mail including charting and trades.
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