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On February 28, 2008, the National Institute of Allergy and Infectious Diseases (NIAID) reported that the protocol for ACTG 5202 is being modified because of reduced virologic response in a subset of patients who were receiving abacavir/3TC. This highly anticipated, phase III, multicenter trial involves 1858 HIV-infected adults in the U.S. who were randomized to begin antiretroviral therapy with one of four regimens:
Efavirenz + tenofovir/FTC
Efavirenz + abacavir/3TC
Ritonavir-boosted atazanavir + tenofovir/FTC
Ritonavir-boosted atazanavir + abacavir/3TC
The comparison between NRTI backbones is double-blinded, with patients taking a placebo pill for whichever NRTI combination they are not receiving. The comparison between efavirenz and boosted a…