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Opiant Pharmaceuticals announces development of OPNT003 for treatment of opioid overdose

Santa Monica, California
Wednesday, February 14, 2018, 11:00 Hrs  [IST]

Opiant Pharmaceuticals, a specialty pharmaceutical company developing pharmacological treatments for addictions, announced positive data from a phase I clinical study of its product candidate OPNT003 (intranasal nalmefene), and provided an update on a meeting held February 8, 2018 with the US Food and Drug Administration (FDA) regarding its planned development program. OPNT003 is in development as a long-lasting opioid antagonist for the treatment of opioid overdose. Based on feedback from the FDA in connection with this meeting, Opiant intends to pursue a 505(b)(2) development path, and anticipates the potential to submit a New Drug Application (NDA) for the drug and intranasal delivery device combination in 2020. Nalmefene for injection was previously approved by the FDA for treating suspected or confirmed opioid overdose. The 505(b)(2) pathway allows companies to rely in part on the FDA's findings of safety and efficacy of a previously approved product and to supplement these findings with a more limited set of their own studies to satisfy FDA requirements, as opposed to conducting the full array of preclinical and clinical studies that would typically be required.

Data generated in a phase I study completed under a clinical trial agreement with the National Institute on Drug Abuse (NIDA) provided the basis for the FDA meeting. These data demonstrate that an intranasal nalmefene formulation containing a proprietary absorption enhancer (Intravail, from Aegis Therapeutics) resulted in rapid increases in plasma levels with an onset faster than an intramuscular injection and a comparatively long half-life (6.7-7.8 hours). Naloxone, the only FDA medication currently approved to treat opioid overdose, has a half-life of approximately 2 hours.

"We are pleased with the positive outcome of this meeting and the beneficial guidance received from the FDA," said Roger Crystal, M.D., chief executive officer of Opiant. "We now have a well-defined development and regulatory pathway to pursue approval of OPNT003 in the US for the treatment of opioid overdose. Following the feedback received from the FDA, we are focused on leveraging the 505(b)(2) development pathway that allows certain information required for NDA approval to be derived from studies not conducted by Opiant. We anticipate submitting an NDA for OPNT003 in 2020. Based on its profile and the phase I trial results, we believe OPNT003 has the potential to be a transformative treatment for opioid overdose, a growing US health epidemic."

"Opiant has full commercial rights to OPNT003 and has submitted a grant application to the National Institutes of Health (NIH) to fund its development to an NDA ready stage," continued Dr. Crystal. "Based on the NIH calling for longer-acting overdose-reversal drugs, we are optimistic that this grant will be funded."

Synthetic opioids, such as fentanyl, are now responsible for more overdose deaths than either heroin or prescription opioids, with over 20,000 synthetic opioid overdose deaths in 2016. Fentanyl and derivatives, such as carfentanil, are especially dangerous because of a long half-life of seven to ten hours that may require repeated dosing of naloxone to overdose victims to prevent relapse. A long-lasting overdose-reversal drug may reduce this burden.

NIH leadership recently called for the development of " stronger, longer-acting formulations of antagonists to counteract the very high potency synthetic opioids that are now claiming thousands of lives each year." (Volkow and Collins, NEJM 2017)

An easy-to-use nasal formulation of nalmefene with a rapid onset and long duration of action would be a ready-to-use tool for non-medically trained persons to administer. If approved by the FDA, OPNT003 may be especially useful in rural areas, where a rapidly growing number of overdoses are occurring, and where access to emergency medical response may be delayed by hours.

 

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