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FDA Approves Foundation Medicine Liquid Biopsy Test As Companion Diagnostic For Lynparza

 
• By Marion Webb

The US FDA expanded the use of FoundationOne Liquid CDx as a companion diagnostic for certain prostate cancer patients eligible for treatment with olaparib.

Lab technician assistant analyzing a blood sample in test tube at laboratory

Foundation Medicine Inc. announced on 9 November that the US Food and Drug Administration has approved its FoundationOne Liquid CDx test for use as a companion diagnostic with AstraZeneca PLC and Merck & Co., Inc.’s Lynparza (olaparib)

Cambridge, MA-based Foundation Medicine, a Roche Holding AG subsidiary, said it will use a blood-based biopsy to detect BRCA1, BRCA2, or ATM genomic alterations in men with metastatic castration-resistant prostate cancer (mCRPC) who are eligible for treatment with olaparib

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