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Buprenorphine Extended-Release Subcutaneous Injection (RBP-6000) in High-risk Users

Completed · Phase 4 · NCT04995029

Conditions: Moderate to Severe Opioid-use Disorder

At a glance

Research payments reported, 2025
$201,905
U.S. investigators named
6
Sites paid
10
Planned or actual enrollment
785

About the trial

Sponsor
Indivior Inc.
Tested
Transmucosal Buprenorphine (drug), Extended-release Buprenorphine (drug)
Dates
Started 2021-10-26; completion 2024-06-26
Results posted
Yes

The primary objective of the induction phase of the study is to compare treatment retention of participants following rapid induction or standard of care (SoC) induction onto extended-release buprenorphine. The primary objective of the maintenance phase is to compare the efficacy of 100 mg and 300 mg maintenance doses of extended-release buprenorphine administered every 4 weeks.

From ClinicalTrials.gov, last updated 2026-02-06. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Indivior Inc. reported $201,905 in research payments for this study in 2025 (586 payments).

Products named: Sublocade

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.