Lexicon Pharmaceuticals has not completely given up on sotagliflozin after the US Food and Drug Administration issued a “deficiencies preclude discussion” letter regarding the new drug application (NDA) seeking approval to treat adults with type 1 diabetes and chronic kidney disease (CKD). However, Lexicon said on 22 November that it will restructure, shuttering its commercial organization and ending promotion of sotagliflozin in its approved heart failure indication.
Key Takeaways
- The US FDA said there were deficiencies in Lexicon’s NDA for Zynquista (sotagliflozin) as a treatment for type 1 diabetes patients with CKD that preclude...
The Woodlands, TX-based Lexicon received notification from the FDA that there were deficiencies in the NDA for Zynquista (sotagliflozin) as an adjunct to insulin in type 1 diabetes patients with...
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