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TEST:
cobas® HPV test

Company:
Roche
Type:
FDA Approved
Related tests:

Details

Evidence
cobas® HPV test is a qualitative in-vitro real-time PCR test designed to detect 14 high-risk human papillomavirus (HPV) genotypes in cervical samples. It is indicated for use for routine cervical cancer screening according to professional medical guidelines. This includes testing patients with abnormal cervical cells, co-testing (adjunctive screen) with tests that use cells to diagnose or screen for cancer, and screening patients older than 25 years old for cervical cancer. It is for use on the fully automated, high-throughput cobas® 6800/8800 Systems.
Cancer:
Cervical Cancer
Method:
PCR
Approvals
Date
Cancer
Gene
Drug
By
04/19/11
FDA
11/06/23
FDA
Confirmatory trial(s)