Agendia’s MammaPrint First and Only Genomic Assay to Receive Level 1A Clinical Utility Evidence for Chemotherapy Benefit in Early Breast Cancer Patients
Clinical high-risk patients with a low-risk MammaPrint® result, including 48 Read More
Clinical high-risk patients with a low-risk MammaPrint® result, including 48 Read More
Company will also host a lunch symposium on genomic assays Read More
Agendia is disappointed with the recent update to the American Read More
IRVINE, CA and AMSTERDAM, THE NETHERLANDS – Agendia, Inc. and Read More
Satellite Symposium and Dinner Presentation Will Offer Latest Insights on Genomic Read More
Researchers Present Data at Breast Cancer Symposium Showing MammaPrint/BluePrint Can Identify Read More
IRVINE, CA and AMSTERDAM – Agendia, Inc., a world leader Read More
Respected Panel Cites RASTER, the Only Published Prospective Outcome Data Read More
Company Also Highlights FDA Clearance of MammaPrint in FFPE IRVINE, Read More