Industry News

FDA Approves FoundationOne CDx for Entrectinib

On June 9, 2022, the U.S. Food and Drug Administration (FDA) approved the FoundationOne®CDx as a companion diagnostic for two entrectinib indications:

  1. To identify patients with ROS1-positive non-small cell lung cancer

  2. To identify patients with neurotrophic tyrosine receptor kinase fusion-positive solid tumors.

Both indications are for patients who may be appropriate for treatment with entrectinib.

For more information, read Foundation Medicine's announcement and Roche's announcement.

Posted 6/9/2022

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