Gilead Sciences

Stories

FDA approves Gilead's Bixlenvo, a single-tablet option for HIV patients on complex regimens

Developer and marketer of Bixlenvo

Roughly 5% of Americans living with HIV take their antiretrovirals as several pills a day, because resistance, side effects, or other medications rule out standard single tablets. On Thursday the FDA approved a pill built for that group.

Updated Aug 27

FDA clears Trodelvy as a first-line treatment for triple-negative breast cancer

New Capabilities

Maker of Trodelvy; holds the new first-line approval

Triple-negative breast cancer is aggressive and short on options. On June 24, 2026, the U.S. Food and Drug Administration cleared Gilead Sciences' Trodelvy as a first-line treatment, moving a drug once used only after other therapies failed to the front of the line. Six days earlier, the European Commission had done the same for patients in the EU who are ineligible for immunotherapy.

Updated Jun 25