FDA Approves MyChoice CDx to Expand Access to Niraparib in Ovarian Cancer
The U.S. Food and Drug Administration has approved MyChoice® CDx as the first companion diagnostic test to identify patients with HRD-positive advanced ovarian cancer who can benefit from the PARP inhibitor niraparib. MyChoice CDx uses advanced genetic sequencing to analyze BRCA1/2 genes and signs of genomic instability, helping find about 34% more eligible patients compared […]
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