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  • Friday, 23 October 2020

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FoundationOne�CDx Receives FDA-Approval as a Companion Diagnostic for VITRAKVI�(larotrectinib) to Identify Patients with NTRK Fusions ...

Posted 2020-10-23, Business Wire

CAMBRIDGE, Mass.--(BUSINESS WIRE)--Foundation Medicine, Inc. today announced that it has received approval from the U.S. Food and Drug Administration (FDA) for

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FDA approves FoundationOne®CDx as companion diagnostic for Vitrakvi™ (larotrectinib) to aid in identifying NTRK fusion-positive patients

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Sumitomo Dainippon Pharma Oncology Announces First Patient Dosed in the Dubermatinib Arm of The Leukemia & Lymphoma Society's Beat AML Master Clinical Trial in Patients with Acute Myeloid Leukemia

CAMBRIDGE, Mass., Oct. 23, 2020 /PRNewswire/ -- Sumitomo Dainippon Pharma Oncology, Inc., a developer of novel cancer therapeutics, today announced the first patient has...

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FoundationOne®CDx Receives FDA-Approval as a Companion Diagnostic for VITRAKVI®(larotrectinib) to Identify Patients with NTRK Fusions ...

The Marshall News Messenger 2020-10-23

FDA Approves FoundationOne�CDx as Companion Diagnostic for Vitrakvi� (larotrectinib), to Aid in Identifying NTRK Fusion-Positive Patients

Business Wire 2020-10-23

FDA Approves FoundationOne®CDx as Companion Diagnostic for Vitrakvi® (larotrectinib), to Aid in Identifying NTRK Fusion-Positive Patients

The Marshall News Messenger 2020-10-23

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