drugset / Trial / NCT02801357

Study to Evaluate the Exposures of Lofexidine and Its Major Metabolites in Subjects Seeking Buprenorphine Dose Reduction

NCT02801357

Phase 1 Completed 10 enrolled USWM, LLC (dba US WorldMeds)
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the relative exposures of lofexidine and its major metabolites in subjects seeking buprenorphine dose reduction.

Timeline

Start
2016-06
Primary completion
2016-08
Completion
2016-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Lofexidine Small molecule 0.8 mg