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Ensysce Biosciences To Present Oral Overdose Protection For Opioids At The 5th Annual NIH HEAL Meeting

Author: Benzinga Newsdesk | January 25, 2024 09:04am
Ensysce Biosciences, Inc. ("Ensysce" or the "Company") (NASDAQ:ENSC), a clinical-stage biotech company applying transformative chemistry to improve prescription drug safety to reduce abuse and overdose, today announced

Ensysce Biosciences, Inc. ("Ensysce" or the "Company") (NASDAQ:ENSC), a clinical-stage biotech company applying transformative chemistry to improve prescription drug safety to reduce abuse and overdose, today announced that Geoff Birkett, Chief Commercial Officer of Ensysce, will present a poster entitled "PF614-MPAR: A Novel Trypsin Activated Abuse Protected (TAAP™) Extended-Release Oxycodone Prodrug with Overdose Protection" at the Annual National Institutes of Health (NIH) "Helping to End Addiction Long-term" (HEAL) Initiative Scientific Meeting being held on February 7 and 8, 2024, in Bethesda, MD.

PF614-MPAR, the lead product under Ensysce's oral overdose protection platform, MPAR® (Multi-Pill Abuse Resistance), was just granted Breakthrough Therapy Designation by the U.S. Food and Drug Administration (FDA) and has been supported by funding from the National Institute on Drug Abuse (NIDA). The endorsements by both agencies have aided the clinical development of the first opioid with both abuse deterrent properties and importantly, oral overdose protection. We believe that no opioid on the market has these dual properties. The trial being presented was undertaken to optimize the PF614-MPAR combination drug product and successfully met its overdose protection endpoints.

"Noting the latest CDC data on prescription overdoses citing that we lose two people every hour has my team laser focused on ensuring Ensysce's drug products can be effective in reducing these numbers," said Dr. Lynn Kirkpatrick, Chief Executive Officer of Ensysce Biosciences. "We are grateful for the support of the NIH HEAL Initiative program and NIDA, and the corresponding funding which has been instrumental in advancing our efforts into combatting abuse and protecting against oral opioid overdose. The FDA BTD will also greatly assist in accelerating the development of PF614-MPAR, potentially a first-in-class ‘Next Generation' opioid designed to treat severe pain with these essential protective properties."

Geoff Birkett, CCO, added, "The Ensysce team is pleased with the exceptional data we were able to generate for our MPAR® platform and our lead agent, PF614-MPAR. The US opioid crisis has not been impacted by a new approach to address abuse for over the last two decades. Ensysce intends to change that with what we believe are disruptive platforms, TAAP and MPAR. We also believe our safer medications will address the growing issue of patients' lack of access to analgesics to treat severe pain, a situation caused by the opioid crisis."

Posted In: ENSC

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