drugset / Trial / NCT04070157

Randomized, Double-Blind, Placebo-Controlled Pilot Study on the Safety and Effectiveness of LUCEMYRA During an Opioid Taper in Treatment of Withdrawal

NCT04070157 ↗

Phase 2 Terminated 4 enrolled USWM, LLC (dba US WorldMeds)
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Stopping prescription opioid pain medications can be difficult due to withdrawal symptoms. This study will test if LUCEMYRA helps reduce withdrawal symptoms and helps more people reduce their opioid dose compared to placebo.

Timeline

Start
2019-08-02
Primary completion
2019-11-27
Completion
2019-11-27

Outcome

Outcome not reported

Stopped (Enrollment): “COVID pandemic and enrollment issues necessitating an adjustment to the study design.”

Drugs

EvaluationDrugModalityDoseRoute
Subject Lofexidine Small molecule 0.18 mg —