Tag: Trodelvy
Sacituzumab Govitecan Expected to Become Gilead’s Blockbuster Following Expanded Approval
In early February this year, the U.S. Food and Drug Administration (FDA) approved sacituzumab govitecan-hziy (Trodelvy®; Gilead Sciences) for the treatment of adult patients with...
Gilead Agrees to Collaborate on the Strata Precision Indications for Approved...
Gilead Sciences and Strata Oncology have signed an agreement in which Gilead has agreed to collaborate on the Strata Precision Indications for Approved THerapies (Strata PATH™; NCT05097599) study by providing sacituzumab govitecan-hziy (Trodelvy®) for eligible patients with cancer.
Sacituzumab Govitecan Demonstrates Clinical Efficacy Across Trop-2 Expression Levels in HR+/HER2-...
Results from a post-hoc analysis from the Phase 3 TROPiCS-02 study evaluating sacituzumab govitecan-hziy (Trodelvy®; Gilead Sciences) versus comparator chemotherapy (physicians’ choice of chemotherapy, TPC) in patients...
What to Expect at ESMO 2022: Sacituzumab Govitecan Show PFS Benefits...
New data from a post hoc subgroup analysis from the Phase 3 TROPiCS-02 study evaluating sacituzumab govitecan-hziy* (Trodelvy®, Gilead Sciences) versus comparator chemotherapies (physicians’...
Sacituzumab Govitecan Approved in China for Second-Line Metastatic Triple-Negative Breast Cancer
China's National Medical Products Administration (NMPA) has approved sacituzumab govitecan (Trodelvy®; Gilead Sciences) for the treatment of adult patients with unresectable locally advanced or metastatic...
Sacituzumab Govitecan Increases PFS for Patients With Most Common Type of...
Treatment with sacituzumab govitecan (Trodelvy®; Gilead Sciences), an antibody-drug conjugate (ADC), resulted in longer progression-free survival (PFS) compared to physician’s choice of chemotherapy in...
Sacituzumab Govitecan Receives European Marketing Authorization for the Treatment of mTNBC...
The European Commission (EC) has granted marketing authorization for sacituzumab govitecan (Trodelvy®; Gilead Sciences) a first-in-class topoisomerase inhibitor antibody-drug conjugate (ADC) directed to the...
Shanghai Fudan-Zhangjiang’s FDA018-ADC Enters Phase I Clinical Trials
The National Medical Products Administration of the People's Republic of China has accepted Shanghai Fudan-Zhangjiang Bio-Pharmaceutical’s request to allow FDA018-ADC to enter in phase...
Withdrawal of FDA’s Accelerate Approved Therapeutic Agents may harm Patients
The United States Food and Drug Administration’s (FDA) program to accelerate approval of some promising therapeutic agents has recently come under fire due to...
Sacituzumab Govitecan Receives Accelerated Approval for Advanced or Metastatic Urothelial Cancer...
The U.S. Food and Drug Administration (FDA) has granted accelerated approval to Gilead Sciences* Sacituzumab Govitecan** (Trodelvy®) for use in adult patients with locally...
