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Published on 7 December 2009

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Visanne cleared for market launch in Europe

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Bayer Schering Pharma AG, Germany, has successfully
completed the decentralised part of drug approval procedure in Europe for a new treatment of endometriosis called Visanne.

Visanne is a once-daily oral tablet containing dienogest 2mg that has been developed specifically for the treatment of endometriosis.

A dedicated clinical study programme has proven that Visanne relieves endometriosis pain with high efficacy, reduces endometriosis lesions and demonstrates a favourable safety
and tolerability profile. Market launch of the product is planned from the second quarter 2010 onwards.

“With Visanne, we will be able to offer women a new treatment option which can reduce the substantial burden of endometriosis,” said Phil Smits, MD, Head of Bayer Schering
Pharma’s Business Unit Women’s Healthcare. “Surgical treatment of endometrosis is associated with high relapse rates and many currently available medical therapy options have side effects which do not allow for long-term use. Patients often need to use different combinations of the available treatment options and even undergo repeat surgical procedures.

There is therefore a high medical need for new treatment options.” The current standard therapy (regarding efficacy), GnRH analogue, can only be used for the short-term relief of symptoms associated with endometriosis, as safety concerns such as decreased bone mineral density and side effects such as hot flushes limit its long-term use. Visanne has been shown to be as effective as GnRH analogue and to be superior to
placebo in reducing pain related to endometriosis. Pain relief is sustained over time (shown in a clinical study lasting 15 months) and includes dysmenorrhea-like pain, premenstrual
pain, diffuse pelvic pain and dyspareunia.

Bayer



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