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Home › FDA Grants IDE Approval for Almac Diagnostic Services' CDx for Use in Cancer Drug Study

FDA Grants IDE Approval for Almac Diagnostic Services' CDx for Use in Cancer Drug Study

May 06, 2019
|
staff reporter

NEW YORK (GenomeWeb) – Turning Point Therapeutics and Almac Diagnostic Services today announced approval by the US Food and Drug Administration of an investigational device exemption for use of an Almac diagnostic assay to determine whether cancer patients are eligible to enroll in a Phase II clinical study.

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