FDA Accepts Zealand's GLP-1 Drug Lixisenatide for Review
By Cormac Sheridan
Wednesday, February 20, 2013
The FDA accepted for review a new drug application for lixisenatide, the once-daily glucagon-like peptide-1 (GLP-1) receptor agonist Zealand Pharma A/S has developed in partnership with Sanofi SA, paving the way for a possible U.S. approval in Type II diabetes by early 2014.
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