| Literature DB >> 23392460 |
Andrew Zolopa1, Paul E Sax, Edwin DeJesus, Anthony Mills, Calvin Cohen, David Wohl, Joel E Gallant, Hui C Liu, Andrew Plummer, Kirsten L White, Andrew K Cheng, Martin S Rhee, Javier Szwarcberg.
Abstract
We report week 96 results from a phase 3 trial of elvitegravir/cobicistat/emtricitabine/tenofovir disoproxil fumarate (EVG/COBI/FTC/TDF, n = 348) vs efavirenz/emtricitabine/tenofovir disoproxil fumarate (EFV/FTC/TDF, n = 352). At week 48, EVG/COBI/FTC/TDF was noninferior to EFV/FTC/TDF (88% vs 84%, difference +3.6%, 95% confidence interval: -1.6% to 8.8%). Virologic success (HIV-1 RNA <50 copies/mL) was maintained at week 96 (84% vs 82%, difference +2.7%, 95% CI: -2.9% to 8.3%). Discontinuation due to adverse events was low (5% vs 7%). Median changes in serum creatinine (mg/dL) at week 96 were similar to week 48. These results support the durable efficacy and long-term safety of EVG/COBI/FTC/TDF.Entities:
Mesh:
Substances:
Year: 2013 PMID: 23392460 DOI: 10.1097/QAI.0b013e318289545c
Source DB: PubMed Journal: J Acquir Immune Defic Syndr ISSN: 1525-4135 Impact factor: 3.731