Abstract
There is an urgent need for new pharmacological treatments for substance use disorders, including opioid use disorder, particularly for use in relapse prevention. A combination of buprenorphine with naltrexone has shown particular promise, with clinical studies indicating a substantial improvement over treatment with naltrexone alone. OREX-1019 (formerly BU10119) is a compound that mimics the pharmacology of the buprenorphine/naltrexone combination. This study evaluated, in rhesus monkeys, the therapeutic potential of OREX-1019 for treating opioid use disorder. Pretreatment with OREX-1019 (0.01-0.3 mg/kg s.c.) dose-dependently decreased responding for the m opioid receptor agonist remifentanil in rhesus monkeys but did not maintain levels of responding above vehicle when it was available for self-administration. OREX-1019 (0.01-1.0 mg/kg s.c.) also decreased cue- plus heroin-primed reinstatement of extinguished responding in monkeys that self-administered remifentanil but did not alter cue- plus cocaine-primed reinstatement of responding in monkeys that self-administered cocaine. OREX-1019 (0.3 mg/kg s.c.), like naltrexone (0.1 mg/kg s.c.), increased heart rate and blood pressure, produced overt observable signs, and eliminated food-maintained responding in monkeys treated chronically with morphine. These results confirm that OREX-1019 has little or no efficacy at m opioid receptorsand has low abuse potential, and, combined with promising safety (clean profile vs. other off-target proteins including the hERG (human ether-a-go-go-related gene) K 1 channel) and pharmacokinetic data (supporting administration by subcutaneous or sublingual routes, but with low oral bioavailability), suggest it could be a safe and effective alternative to current treatments for opioid use disorders particularly as applied to relapse prevention.
Original language | English |
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Pages (from-to) | 205-215 |
Journal | Journal of Pharmacology and Experimental Therapeutics |
Volume | 372 |
Issue number | 2 |
Early online date | 20 Nov 2019 |
DOIs | |
Publication status | Published - 1 Feb 2020 |
Bibliographical note
Funding Information:The majority of this work was supported by Orexigen Therapeutics and, in part, supported by the National Institutes of Health National Institute on Drug Abuse [Grant R01DA07315 (S.M.H.)]. B.B. and P.F. were employed by Orexigen Therapeutics while engaged in this research project. S.M.H. is an inventor on the patent that describes OREX-1019/BU10119 and was a consultant to Orexigen Therapeutics during this project. https://doi.org/10.1124/jpet.119.261511. s This article has supplemental material available at jpet.aspetjournals.org.
Publisher Copyright:
© 2020 by The American Society for Pharmacology and Experimental Therapeutics
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