The first quarter of the year saw two notable FDA approvals for HIV therapies. In early February, Gilead Sciences gained approval for its triple combination product Biktarvy, which brings together the novel HIV-1 integrase inhibitor bictegravir with the established dual nucleoside reverse transcriptase inhibitor (NRTI) backbone of emtricitabine and tenofovir alafenamide in a once-daily, oral tablet formulation. Biktarvy is set to be one of 2018’s biggest launches and Gilead’s largest growth driver, with forecast sales of more than US$5 billion in 2022…

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Fonte: NATURE REVIEWS | DRUG DISCOVERY VOLUME 17 | MAY 2018 | 309