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FDA OKs expanded use of Roche cervical cancer test

September 16, 2020

The FDA approves expanded use of Roche’s (OTCQX:RHHBY) CINtec PLUS Cytology test to be used as triage for positive cobas HPV tests performed on the automated cobas 6800 and 8800 systems in primary screening or co-testing programs.

The company says CINtec PLUS is more sensitive than a PAP smear and allows physicians to determine which HPV-positive women require further diagnostic procedures to prevent disease progression.

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