Clinical trial
A Randomized, Double-Blind Study of the Safety and Efficacy of GSK1349572 Plus Abacavir/Lamivudine Fixed-Dose Combination Therapy Administered Once Daily Compared to Atripla Over 96 Weeks in HIV-1 Infected Antiretroviral Therapy Naive Adult Subjects
NCT01263015 is registered in ClinicalTrials.gov with ViiV Healthcare as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Randomized, Double-Blind Study of the Safety and Efficacy of GSK1349572 Plus Abacavir/Lamivudine Fixed-Dose Combination Therapy Administered Once Daily Compared to Atripla Over 96 Weeks in HIV-1 Infected Antiretroviral Therapy Naive Adult Subjects
- Lead sponsor
- ViiV Healthcare
- Phase
- Phase 3
- Overall status
- Completed
- Start date
- February 1, 2011
- Completion date
- December 3, 2015
- Enrollment
- 844 (actual)
- Sites
- 145
Conditions
As the registry lists them; a condition with its own page is linked.
infection, human immunodeficiency virus i