U.S. FDA approves NADiA ProsVue prognostic test for prostate cancer

According to a media release issued on Thursday by IRIS International, the U.S. Food & Drug Administration (FDA) has approved the company’s NADiA® ProsVue™ test as a prognostic marker that can “aid in identifying” men at reduced risk for recurrence of prostate cancer in the first 8 years after a prostatectomy.

A prognostic test for low risk of progression post-surgery

IRIS Molecular Diagnostics has submitted an application to the U.S. Food and Drug Administration to market a prostate cancer prognostic test called NADiA® ProsVue™.  The company says that this test is “designed to help physicians identify patients at low risk of cancer recurrence post radical prostatectomy.”

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