Bictegravir
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Bictegravir (INN; BIC, formerly known as GS-9883) is a second-generation integrase inhibitor (INSTI) class that was structurally derived from an earlier compound dolutegravir by scientists at Gilead Sciences. See also Bictegravir. In 2016, bictegravir was in a Phase 3 trial as part of a single tablet regimen in combination with tenofovir alafenamide (TAF) and emtricitabine (FTC) for the treatment of HIV-1 infection[1] and the combination drug bictegravir/emtricitabine/tenofovir alafenamide (Biktarvy) was approved for use in the United States in 2018.[2] Structure of the STLV intasome:B56 complex bound to the strand-transfer inhibitor bictegravir (7ouh). Bictegravir inhibits integrase.
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This page was last modified 12:32, 29 August 2023.