AstraZeneca says FDA approves Etcamah-CDK4/6 combo for first-line advanced HR-positive breast cancer

Reuters2026/09/04 20:34

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FDA granted accelerated clearance for AstraZeneca’s Etcamah with a CDK4/6 inhibitor in first-line advanced HR-positive, HER2-negative breast cancer.
Use targets patients who develop an emergent ESR1 mutation during aromatase inhibitor treatment, confirmed via an FDA-authorized test.
SERENA-6 data showed a 56% lower risk of progression or death versus standard care; median PFS 16 months versus 9.2.

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. AstraZeneca plc published the original content used to generate this news brief on September 04, 2026, and is solely responsible for the information contained therein.

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AstraZeneca says FDA approves Etcamah-CDK4/6 combo for first-line advanced HR-positive breast cancer

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