FDA accepts Zynquista NDA for review

23 May 2018

The US Food and Drug Administration (FDA) has accepted a regulatory filing for Zynquista (sotagliflozin) from French pharma major Sanofi (Euronext: SAN) and partner Lexicon Pharmaceuticals (Nasdaq: LXRX).

The investigational oral treatment would be used in addition to insulin therapy to improve blood sugar control in adults with type 1 diabetes.

In March this year the European Medicines Agency accepted the companies’ regulatory submission for the dual inhibitor of SGLT-1 and SGLT-2.

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