drugset / Trial / NCT02386098

Strategy-confirming Study of BMS-955176 to Treat HIV-1 Infected Treatment-experienced Adults

NCT02386098

Phase 2 Terminated 86 enrolled ViiV Healthcare GlaxoSmithKline · collab
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate whether the combination of BMS-955176 with atazanavir (ATV) \[with or without ritonavir (RTV)\] and dolutegravir (DTG) is efficacious, safe, and well-tolerated in HIV-1 infected treatment experienced adults.

Timeline

Start
2015-07-08
Primary completion
2017-06-07
Completion
2017-06-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Atazanavir Other / unclassified 300 mg Oral
Subject Atazanavir Other / unclassified 400 mg Oral
Subject BMS-955176 Other / unclassified 120 mg Oral
Subject BMS-955176 Other / unclassified 180 mg Oral
Subject Tenofovir Small molecule 300 mg Oral
Background Dolutegravir Other / unclassified 50 mg Oral
Background Ritonavir Other / unclassified 100 mg Oral