California’s Gilead Sciences (Nasdaq: GILD) has announced 48-week data from a Phase III study looking at the efficacy and safety of switching HIV patients to a fixed-dose combination of bictegravir plus emtricitabine/tenofovir alafenamide.
Patients in the ongoing study, who were switched from a multi-tablet regimen, did not have inferior outcomes, and demonstrated no treatment-emergent resistance.
Gilead, which has seen business drop off at its key HCV division as the number of new patients starts to decline, has been looking to boost sales in other areas.
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