| Literature DB >> 23807156 |
Richard Elion1, Jean-Michel Molina, José Ramón Arribas López, David Cooper, Franco Maggiolo, Edmund Wilkins, Brian Conway, Ya-Pei Liu, Nicolas Margot, Martin Rhee, Steven L Chuck, Javier Szwarcberg.
Abstract
: This 96-week, double-blind, active-controlled, phase 3 study, randomized subjects to elvitegravir once daily or raltegravir twice daily with a fully active, ritonavir-boosted protease inhibitor plus a third agent. The proportion of subjects randomized to elvitegravir that achieved and maintained HIV-1 RNA < 50 copies/mL through week 96 was 47.6% (167/351) compared with 45.0% (158/351) for raltegravir with a treatment difference of 2.6% (95% confidence interval: 4.6% to 9.9%). Both regimens were well tolerated, with comparable rates of adverse events and laboratory abnormalities through week 96. Once-daily elvitegravir was noninferior to twice-daily raltegravir, showed durable long-term efficacy, and was well tolerated in HIV+ treatment-experienced patients.Entities:
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Year: 2013 PMID: 23807156 DOI: 10.1097/QAI.0b013e318298469c
Source DB: PubMed Journal: J Acquir Immune Defic Syndr ISSN: 1525-4135 Impact factor: 3.731