drugset / Trial / NCT01384734

HIV Attachment Inhibitor to Treat Human Immunodeficiency Virus 1 (HIV-1) Infections

NCT01384734

Phase 2 Completed 254 enrolled ViiV Healthcare
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to assess the safety, efficacy, tolerability and pharmacokinetics of four doses of BMS-663068 with Raltegravir (RAL) + Tenofovir Disoproxil Fumarate (TDF). At least 1 dose of BMS-663068 can be identified which is safe, well tolerated, and efficacious when combined with RAL + TDF for treatment-experienced HIV-1 infected subjects. PHENOSENSE® is a registered trademark of Monogram Biosciences.

Timeline

Start
2011-07-26
Primary completion
2013-02-18
Completion
2017-05-12

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Atazanavir Other / unclassified 300 mg Oral
Subject Fostemsavir Other / unclassified 400 mg Oral
Subject Fostemsavir Other / unclassified 600 mg Oral
Subject Fostemsavir Other / unclassified 800 mg Oral
Subject Fostemsavir Other / unclassified 1200 mg Oral
Comparator Ritonavir Other / unclassified 100 mg Oral
Background Raltegravir Other / unclassified 400 mg Oral
Background Tenofovir Small molecule 300 mg Oral