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. Disposition of individuals at Week 48.
AE, adverse event; MVC, maraviroc; DRV/r, darunavir/ritonavir; TDF/FTC, tenofovir/emtricitabine. aOf the AEs leading to discontinuation, 12 in each group were considered to be related to study treatment. bInvestigator decision to discontinue for lack of efficacy; individual did not necessarily meet criteria for protocol-defined virologic failure.
