drugset / Trial / NCT03993392

SUBLOCADE Rapid Initiation Study

NCT03993392

Phase 4 Completed 26 enrolled Indivior Inc.
NaSingle-groupOpen-labelTreatment

Summary

This study is to evaluate the safety and tolerability of initiating SUBLOCADE™ treatment following a shorter period of transmucosal (TM) buprenorphine treatment.

Timeline

Start
2019-08-29
Primary completion
2019-12-26
Completion
2019-12-26

Drugs

EvaluationDrugModalityDoseRoute
Subject Buprenorphine Other / unclassified 300 mg Subcutaneous
Subject Buprenorphine Other / unclassified 4 mg Other

Indications