Abstract
Doravirine is a nonnucleoside reverse transcriptase inhibitor that has been approved for the treatment of HIV-1. In a phase 1 trial, doravirine exposure was transiently decreased when treatment was started immediately after the cessation of efavirenz treatment. In a post hoc subgroup analysis of participants who switched from an efavirenz-based regimen to doravirine-lamivudine-tenofovir disoproxil fumarate in the phase 3 DRIVE-SHIFT trial, doravirine plasma levels at week 4 were similar to noninduced levels, and HIV-1 suppression was maintained at weeks 24 and 48.
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Greaves, W., Wan, H., Yee, K. L., Kandala, B., Vaddady, P., & Hwang, C. (2019). Doravirine exposure and HIV-1 suppression after switching from an efavirenz-based regimen to doravirine-lamivudine-tenofovir disoproxil fumarate. Antimicrobial Agents and Chemotherapy, 63(12). https://doi.org/10.1128/AAC.01298-19
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