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FDA Approves Companion Diagnostic for Capivasertib Plus Fulvestrant in Advanced HR+/HER2–Breast Cancer

The FDA has approved the FoundationOneĀ® CDx for use as a companion diagnostic to identify patients with advanced hormone receptorā€“positive, HER2-negative advanced breast cancer who may be eligible for treatment with the combination of capivasertib and fulvestrant.

U S FDA Approves FoundationOne®CDx as a Companion Diagnostic for AstraZeneca s Truqaptm (capivasertib) in combination with Faslodex® (fulvestrant) to Identify Patients with HR-Positive, HER2-Negative Advanced Breast Cancer

U S FDA Approves FoundationOne®CDx as a Companion Diagnostic for AstraZeneca s Truqaptm (capivasertib) in combination with Faslodex® (fulvestrant) to Identify Patients with HR-Positive, HER2-Negative Advanced Breast Cancer
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