A study for people looking to transition from Buprenorphine maintenance to VIVITROL

A study for people looking to transition from Buprenorphine maintenance to VIVITROL
Recruiting
18 years - 60 years
All
Phase 3
1 Location

Brief description of study

Up to 9 weeks, including Screening (up to 3 weeks), up to 2 weeks for Lead-in Period and residential Treatment Period receiving decreasing doses of Buprenorphine and increasing doses of either active or placebo Naltrexone, 4-5 days for VIVITROL induction and post-VIVITROL monitoring, and a 4-week outpatient follow-up period.

Eligibility of study

You may be eligible for this study if you meet the following criteria:

  • Conditions: Opioid Addiction, Opioid-Related Disorders
  • Age: 18 years - 60 years
  • Gender: All
Updated on 19 Feb 2024. Study ID: 825716

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