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Digene finally able to take DNA HPV (human papillomavirus) test to $400 million market

This article was originally published in Clinica

Executive Summary

The US FDA has approved Digene's DNA test for the human papillomavirus as a primary screening tool for the detection of cervical cancer in women aged 30 and over. It is intended to be used in combination with the 50-year-old Pap smear, the FDA said.

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