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NeoVista, Inc. Announces the Launch of VIDION ANV Therapy System in UK for Treating Wet Age-Related Macular Degeneration
Date:11/16/2009

chance of preserving some or much of their central vision.

About MERLOT Study:
The MERLOT Trial is a multi-centre, randomized, controlled clinical study of the VIDION® ANV Therapy System. It is designed to test the hypothesis that epimacular brachytherapy will reduce the frequency of injections needed by patients to control their disease. A total of 363 patients will be enrolled into the trial.

MERLOT tests the VIDION® ANV® Therapy System in patients who continue to require ongoing and frequent injections to control their disease in the UK. These patients may have a poor quality of life due to repeated frequent visits to hospital. They have the most to gain from a device that may reduce their life long burden of treatment. The study compares the VIDION® ANV® Therapy System to the ongoing standard treatment with intravitreal injection therapy.

About NeoVista, Inc.:
NeoVista, Inc. is a privately held medical device company based in Fremont, California. NeoVista’s epimacular brachytherapy procedure is currently being studied in a definitive Phase III clinical study to support eventual filing for regulatory approval to market the product in the United States. For more information about the company, the clinical trial or this novel wet AMD therapy, please visit the company’s Website at www.neovistainc.com.

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Read the full story at http://www.prweb.com/releases/2009/11/prweb3211804.htm.


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