Drug intelligence / Profile preview

O'Neil long-acting naltrexone implant

Development stage
Unknown
Lead developer
Go Medical Industries
Modality
Small Molecules
Administration
Subcutaneous, Implant
01

Overview

The O'Neil Long-Acting Naltrexone Implant (OLANI) is a biodegradable, subcutaneous implant developed by the Australian pharmaceutical company Go Medical Industries, in collaboration with Dr. George O'Neil. The active ingredient is naltrexone, a small-molecule opioid receptor antagonist that blocks opioid receptors in the brain, reducing or eliminating opioid effects and cravings to prevent relapse. The implant is inserted subcutaneously into the abdominal tissue and is designed to slowly release a controlled, constant dose of naltrexone for up to 6 to 18 months before biodegrading and being fully absorbed by the body. It is intended to treat opioid dependence (opioid use disorder) and alcohol dependence. The OLANI has been evaluated in Phase 2 and Phase 3 clinical trials, including a Phase 3 single-group Australian trial assessing safety and efficacy in people with substance dependence over 12 months post-implantation. The FDA granted an Investigational New Drug (IND) application for the Naltrexone Subcutaneous Implant in 2018.

Other names
OLANIO'Neil Long-Acting Naltrexone ImplantO'Neil Long Acting Naltrexone ImplantNaltrexone Subcutaneous Implant
02

Targets

DOR (Opioid Receptor Delta 1)MOR (Mu opioid receptor)KOR (Kappa opioid receptor)

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