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  • sacituzumab...

Tag: sacituzumab govitecan hziy

You Searched For "sacituzumab govitecan-hziy"
Trodelvy plus Keytruda effective for aggressive breast cancer type: Gilead Sciences

Trodelvy plus Keytruda effective for aggressive breast cancer type: Gilead Sciences

Ruchika Sharma23 April 2025 10:30 AM IST
Foster City: Gilead Sciences, Inc. has announced positive topline results from the Phase 3 ASCENT-04/KEYNOTE-D19 study, demonstrating that...
small cell lung cancer treatment

Gilead Sciences earns USFDA Breakthrough Therapy Designation for lung cancer treatment Trodelvy

Ruchika Sharma19 Dec 2024 1:30 PM IST
Foster City: Gilead Sciences, Inc. has announced that Trodelvy (sacituzumab govitecan-hziy) has received Breakthrough Therapy...
HIV drug kickbacks: Gilead Sciences to pay  USD 202 million to settle lawsuit

Gilead Sciences Trodelvy, Keytruda combo study demonstrates promising clinical activity in first-line Metastatic Non-Small Cell Lung Cancer

Ruchika Sharma12 Sept 2023 2:30 PM IST
Foster City: Gilead Sciences, Inc. has announced promising early data from the global, open-label, Phase 2 EVOKE-02 study evaluating Trodelvy...
Gilead Sciences Trodelvy under USFDA priority review for adult patients with pretreated metastatic breast cancer

Gilead Sciences Trodelvy under USFDA priority review for adult patients with pretreated metastatic breast cancer

Ruchika Sharma14 Oct 2022 2:30 PM IST
Trodelvy (sacituzumab govitecan-hziy) is a first-in-class Trop-2 directed antibody-drug conjugate.
Gilead Sciences cancer drug Trodelvy gets speedy USFDA approval

Gilead Sciences cancer drug Trodelvy gets speedy USFDA approval

Ruchika Sharma14 April 2021 4:11 PM IST
Foster City: Drugmaker, Gilead Sciences, has recently announced that the U.S. Food and Drug Administration (USFDA) has granted accelerated...
Gilead Sciences application for breast cancer therapy gets EMA validation

Gilead Sciences application for breast cancer therapy gets EMA validation

Ruchika Sharma28 March 2021 11:00 AM IST
Foster City: Gilead Sciences has recently announced that the European Medicines Agency (EMA) has validated the Marketing Authorization Application...

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