Amylin Pharmaceuticals Withdraws Swiss Regulatory Application for SYMLIN(R)
"We are currently evaluating our SYMLIN(R) regulatory options in markets in other countries, including resubmission in Switzerland. However, at this time our priority is to gain regulatory approval in the U.S.," said Joann L. Data, MD, PhD, Senior Vice President of Regulatory Affairs and Quality Assurance for Amylin Pharmaceuticals, Inc. "Currently, Amylin's primary focus is to work with the FDA to answer questions posed in the SYMLIN(R) approvable letter received in December 2003."
The revision in Amylin's Swiss regulatory strategy for SYMLIN(R) does not affect regulatory strategies being pursued in the U.S. In December 2003, Amylin received a second Approvable Letter from the Food and Drug Administration (FDA) for both type 1 and insulin-using subjects with type 2 diabetes. Final approval is subject to the outcome of further discussions with the FDA.
Amylin Pharmaceuticals is committed to improving the lives of people with diabetes and other metabolic disorders through the discovery, development and commercialization of innovative, cost-effective medicines. Further information on Amylin Pharmaceuticals and its pipeline in metabolism is available at www.amylin.com .
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