Bayer & Regeneron Start Phase 3 Clinical Program in Diabetic Macular Edema
The two companies are extending their development program for VEGF Trap-Eye in DME after promising results in the global Phase 2 DME program.
Bayer HealthCare and Regeneron Pharmaceuticals, Inc. have launched the first of two Phase 3 clinical trials to evaluate the efficacy and safety of VEGF Trap-Eye (aflibercept ophthalmic solution), an investigational new agent for the treatment of certain eye diseases, in the treatment of Diabetic Macular Edema (DME).
The first Phase 3 trial in DME, named VIVID-DME, is being led by Bayer HealthCare and has started in Australia. The trial will also be conducted in Europe and Japan. A second study led by Regeneron, named VISTA-DME, is expected to begin later in 2011 in the U.S, Canada, and other countries.
The Phase 3 program in DME expands the companies’ global development collaboration for VEGF
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