Endocrinologic and Metabolic Drugs Advisory Committee (May 25)
The committee will discuss the safety and efficacy of new drug applications (NDAs) 208673 for insulin glargine and lixisenatide injection, a fixed ratio drug product consisting of insulin and a GLP-1 receptor agonist, and 208471 for lixisenatide injection, a GLP-1 receptor agonist, submitted by Sanofi Aventis c/o Sanofi U.S. Services Inc., proposed for the treatment of adults with type 2 diabetes mellitus.
Helene Clayton-Jeter, O.D.
Office of Health and Constituent Affairs
Food and Drug Administration
cardio.endo@fda.hhs.gov
Office of Health and Constituent Affairs
Food and Drug Administration
cardio.endo@fda.hhs.gov
For more information about the Cardiovascular & Endocrine Liaison Program visit the FDA Patient Network
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