drugset / Trial / NCT01911845

An Open-label, Single Arm, Phase 2 Study to Evaluate ABT-450/r/ABT-267 and ABT-333 With Ribavirin (RBV) in Adults With Genotype 1 HCV Infection Taking Methadone or Buprenorphine

NCT01911845

Phase 2 Completed 38 enrolled AbbVie
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the safety and efficacy of ABT-450/ritonavir/ABT-267 (ABT-450/r/ABT-267; ABT-450 also known as paritaprevir; ABT-267 also known as ombitasvir) and ABT-333 (also known as dasabuvir) coadministered with ribavirin (RBV) in hepatitis C virus (HCV) genotype 1-infected adults taking methadone or buprenorphine ± naloxone.

Timeline

Start
2013-04
Primary completion
2013-12
Completion
2014-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Ribavirin Small molecule 500 mg Oral
Subject Ribavirin Small molecule 600 mg Oral
Subject Ritonavir Other / unclassified 100 mg Oral
Subject dasabuvir Small molecule 250 mg Oral
Subject ombitasvir Small molecule 25 mg Oral
Subject paritaprevir Small molecule 150 mg Oral