Oral Buprenorphine as a Novel Low-dose Induction Strategy for Opioid Use Disorder

PHASE1CompletedINTERVENTIONAL
Enrollment

18

Participants

Timeline

Start Date

June 4, 2024

Primary Completion Date

October 1, 2025

Study Completion Date

October 1, 2025

Conditions
Opioid Use Disorder
Interventions
DRUG

Buprenorphine

At each visit, the participant will receive a single dose of buprenorphine, either 0.15mg IV, 8mg PO, or 16mg PO. The order for the first dose administered will be fixed to the IV dose, and the subsequent doses will be randomized and counterbalanced to 8mg or 16mg PO.

Trial Locations (1)

02115

Brigham and Women's hospital, Boston

All Listed Sponsors
collaborator

University of Utah

OTHER

lead

Brigham and Women's Hospital

OTHER

NCT06086275 - Oral Buprenorphine as a Novel Low-dose Induction Strategy for Opioid Use Disorder | Biotech Hunter | Biotech Hunter