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CompletedNCT05878210

Evaluating the SUBLOCADE Treatment Exit Strategy

A Phase IV Study to Evaluate the SUBLOCADE Treatment Exit Strategy

Status
Completed
Phase
Study type
Observational
Enrollment
12 (actual)
Sponsor
Indivior Inc. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to observe and assess the successful taper and opioid withdrawal experience after participants stop receiving SUBLOCADE because their healthcare provider determines their disease symptoms have been controlled for at least 9 months and they, together with their healthcare provider, plan to discontinue MOUD.

Detailed description

This is a Phase IV, observational, multicentre, open-label, study in participants with a history of OUD, who have been on SUBLOCADE treatment for at least 12 injections, have had disease symptoms controlled for at least 9 months in the opinion of the healthcare provider, and both healthcare provider and participant plan to discontinue MOUD treatment.

Conditions

Timeline

Start date
2023-11-24
Primary completion
2025-05-09
Completion
2025-05-09
First posted
2023-05-26
Last updated
2026-01-22

Locations

2 sites across 2 countries: United States, Canada

Source: ClinicalTrials.gov record NCT05878210. Inclusion in this directory is not an endorsement.

Evaluating the SUBLOCADE Treatment Exit Strategy (NCT05878210) · Clinical Trials Directory