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

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.

Clinical Study Identifier: TX4766

Contact research investigator to learn more about this study by filling out the form below.


To: Research Study Investigator
Subject: I am interested in participating in your Research Study
Dear Investigator,
I'm interested in learning more about and participating in your research study named: A study for people looking to transition from Buprenorphine maintenance to VIVITROL
I am hoping to hear back from you and discuss details of the study

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