The ink was barely dry on Gilead Sciences, Inc.’s latest earnings report when the company announced another important milestone, the US Food and Drug Administration approval of Trodelvy (sacituzumab govitecan-hziy) based on survival data from the closely watched TROPiCS-02 trial in pretreated HR-positive/HER-negative metastatic breast cancer (HR+/HER2- mBC). The nod is the latest victory the drug maker has chalked up thanks to the large R&D program it also highlighted in its earnings report.
Gilead announced on 3 February the approval of Trodelvy for HR+/HER2 mBC in patients who have received endocrine-based therapy and...







