CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 51 enrolled
Drug / intervention
GSK1349572 (Cohort I) +1 moredrug
Likely dose
GSK1349572 (Cohort I) 50 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00950859
NCT00950859Phase 2Completed

A Pilot Study to Assess the Antiviral Activity of GSK1349572 Containing Regimen in Antiretroviral Therapy (ART)-Experienced, HIV-1-infected Adult Subjects With Raltegravir Resistance

ViiV Healthcare·interventional·Posted Aug 3, 2009·Updated Dec 4, 2015

In Brief

A Phase 2 clinical trial evaluating GSK1349572 (Cohort I) and GSK1349572 (Cohort II) for Infection, Human Immunodeficiency Virus. Completed, enrolled 51 participants across 26 sites in 5 countries.

Detailed Summary

Integrase is an enzyme produced by HIV so that the virus can multiply in the human body. GSK1349572 is a new drug in the integrase inhibitor class that prevents the enzyme from working properly and therefore prevents the virus from multiplying. GSK1349572 has shown to be effective against viruses in a short-term monotherapy study in adults with no previous exposure to integrase inhibitors. The purpose of this study is to determine whether GSK1349572 is effective in the treatment of HIV-infected patients who no longer respond to treatment with the approved integrase inhibitor raltegravir and carry viruses with resistance to this drug. The safety and efficacy of GSK1349572 50mg once daily in combination with the background HIV drugs previously administered (unless discontinuation of a particular drug is required) will be assessed over 10 days (functional monotherapy phase), followed by the evaluation of the safety and efficacy of GSK1349572 given with a new optimised background regimen from Day 11 through at least Week 24.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesCanada, France, Italy, Spain, United States
CollaboratorsGlaxoSmithKline

Timeline

Phase 2CompletedFinished
20102011201220132014201520162017201820192020202120222023202420252026
First PostedAug 3, 2009
Enrollment StartAug 1, 2009
Primary CompletionNov 1, 2010
Study CompletionJan 1, 2015
TodayJul 2, 2026
Enrollment to primary: 1.3 yearsPosted 16.9 years ago

Interventions

GSK1349572 (Cohort I)drug

50 mg once daily

GSK1349572 (Cohort II)drug

50 mg twice daily