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FDA Grants NeoVista's Request to Utilize Novel Wet AMD Treatment in Compassionate Case
Date:12/10/2008

safety and efficacy of NeoVista's epiretinal brachytherapy delivered concomitantly with the FDA-approved anti-VEGF therapy Lucentis(R) (ranibizumab) versus Lucentis alone.

About NeoVista, Inc.

NeoVista, Inc. is a privately held development-stage medical device company based in Fremont, California. NeoVista's epiretinal beta radiation therapy 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 Web site at www.neovistainc.com. For detailed information about the CABERNET clinical trial, please visit the study Web site at www.cabernetstudy.com.

    Contact:  Tony Moses
          O:  510.933.7600
          C:  510.402.3394
          tmoses@neovistainc.com


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