On February 3, 2023, the U.S. Food and Drug Administration (FDA) approved Trodelvy^® (sacituzumab govitecan-hziy) for the treatment of adult patients with unresectable locally advanced or metastatic hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative (IHC 0, IHC 1+ or IHC 2+/ISH–) breast cancer who have received endocrine-based therapy and at least two additional systemic therapies in the metastatic setting.

Click here to review the data.

Please see full Prescribing Information including BOXED WARNING.

TRODELVY, the TRODELVY logo, GILEAD, and the GILEAD logo are trademarks of Gilead Sciences, Inc., or its related companies.

©2023 Gilead Sciences, Inc. All rights reserved. US-TROP-0782 02/23