FDA approves Gilead Trodelvy for first-line metastatic triple-negative breast cancer treatment

Gilead Sciences, Inc.

Gilead Sciences, Inc.

GILD

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  • FDA cleared Gilead’s Trodelvy for first-line unresectable locally advanced or metastatic triple-negative breast cancer across PD-L1 status.
  • Label covers monotherapy for PD-(L)1-ineligible patients; combination with Merck’s Keytruda for PD-L1 CPS ≥10 tumors.
  • Decision based on Phase 3 ASCENT-03 and ASCENT-04 data showing 38% and 35% lower risk of progression or death versus comparators.


Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Gilead Sciences Inc. published the original content used to generate this news brief via Business Wire (Ref. ID: 202606241629BIZWIRE_USPR_____20260519_BW132009) on June 24, 2026, and is solely responsible for the information contained therein.

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