Sanofi Submits NDA to FDA and MAA to EMA

For sotagliflozin, for use in combination with insulin therapy to improve glycemic control in adults with type 1 diabetes

Lexicon Pharmaceuticals announced that its collaborator, Sanofi, has submitted a New Drug Application (NDA) to the U.S. Food and Drug Administration and a Marketing Authorization Application (MAA) to the European Medicines Agency (EMA) for sotagliflozin, an investigational dual SGLT1 and SGLT2 inhibitor, for use in combination with insulin therapy to improve glycemic control in adults with type 1 diabetes mellitus.   “The NDA and MAA submissions for sotagliflozin represent important mile...

Continue reading this story and get 24/7 access to Contract Pharma for FREE


Already a subscriber? Sign in

Keep Up With Our Content. Subscribe To Contract Pharma Newsletters