TRODELVY® (Sacituzumab Govitecan-hziy)

The FDA on February 3, 2023, approved TRODELVY® for 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. TRODELVY® is a product of Gilead Sciences, Inc.