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FDA Grants Marketing Approval to FoundationOne CDx In Vitro Diagnostic

A next generation sequencing for detection of genetic mutations in solid tumours
04 Dec 2017
Targeted Therapy

On 30 November 2017, the US Food and Drug Administration (FDA) granted marketing approval to the FoundationOne CDx (F1CDx, Foundation Medicine, Inc.), a next generation sequencing (NGS) based in vitro diagnostic (IVD) to detect genetic mutations in 324 genes and two genomic signatures in any solid tumour type.

The test can also identify which patients with non-small cell lung cancer (NSCLC), melanoma, breast cancer, colorectal cancer, or ovarian cancer may benefit from 15 different FDA-approved targeted treatment options.

Clinical performance of the test was established through a least burdensome means by comparing the F1CDx to previously FDA-approved companion diagnostic tests that are currently used to determine patient eligibility for certain treatments. Results indicated that the test’s ability to detect select mutation types (substitutions and short insertions and deletions) representative of the entire 324 gene panel is accurate approximately 94.6% of the time.

This is the first device with the FDA’s Breakthrough Device designation to complete the premarket approval (PMA) process, and it is the second IVD authorised under the FDA and Centers for Medicare & Medicaid Services’ (CMS) Parallel Review programme. Under this programme, the CMS issued a proposed US national coverage determination of the F1CDx for Medicare beneficiaries with recurrent, metastatic, or advanced stage IV cancer who have not been previously tested using NGS technology and who continue to remain candidates for further therapy.

The FDA reviewed the F1CDx application using a coordinated, cross-agency approach. The FDA Center for Devices and Radiological Health (CDRH) conducted the clinical review with support from the FDA Oncology Center of Excellence, while CDRH conducted all other review aspects and made the final product approval determination.

Healthcare professionals should report all serious adverse events suspected to be associated with the use of any medicine or device to FDA’s MedWatch Reporting System.

Last update: 04 Dec 2017

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