US diagnostics firm Third Wave Technologies says that a clinical trial for its two human papillomavirus products is underway and the company says it continues to anticipate submitting the applications for approval of those products to the US Food and Drug Administration in 2007.
Clinical trial site initiations and the enrollment of women for the study began in late July and more than 20 sites have been qualified to date. Arthur Waldbaum, president of Downtown Women's Health Care in Denver, USA, one of the clinical sites participating in the trial, noted that "the clinical trial design we are using is well constructed and straightforward, fitting very nicely within our normal procedures for screening women for cervical cancer.
According to Third Wave, the global market for HPV testing is approximately $150.0 million and growing at more than 30% a year. The firm recently announced that, in 2007, it will extend its product range into the chlamydia and gonorrhea tests market, which is worth $200.0 million.
This article is accessible to registered users, to continue reading please register for free. A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.
Login to your accountTry before you buy
7 day trial access
Become a subscriber
Or £77 per month
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed
Chairman, Sanofi Aventis UK
Copyright © The Pharma Letter 2025 | Headless Content Management with Blaze