drugset / Trial / NCT02045693

Drug Interaction & Methadone & Buprenorphine

NCT02045693

Phase 1 Completed 32 enrolled Bristol-Myers Squibb
Non-randomizedParallel-groupOpen-label

Summary

The purpose of this study is to assess the effects of steady state DCV/ASV/BMS-791325 fixed dose combination (FDC) + 75mg BMS-791325 on the Pharmacokinetics (PK) of Methadone in subjects with the stable dose of Methadone and on the PK of Buprenorphine in subjects with the stable dose of Buprenorphine.

Timeline

Start
2014-02
Primary completion
2014-04
Completion
2014-04

Drugs

EvaluationDrugModalityDoseRoute
Comparator Buprenorphine Other / unclassified 8 mg Oral
Comparator Buprenorphine Other / unclassified 24 mg Oral
Subject Methadone Other / unclassified 40 mg Oral
Subject Methadone Other / unclassified 120 mg Oral
Background Asunaprevir Small molecule 200 mg Oral
Background Beclabuvir Small molecule 75 mg Oral
Background Daclatasvir Small molecule 30 mg Oral
Comparator Naloxone Small molecule 2 mg Oral
Comparator Naloxone Small molecule 6 mg Oral