New data show empagliflozin meets endpoint as adjunct to insulin in type 1 diabetes

4 October 2018

Boehringer Ingelheim and Eli Lilly (NYSE: LLY) announced today that empagliflozin met the primary efficacy endpoint, defined as a change from baseline in A1C versus placebo after 26 weeks of treatment, for all doses investigated (2.5, 10 and 25 mg) in the Empagliflozin as Adjunctive to inSulin thErapy (EASE) Phase III program in adults with type 1 diabetes.

The EASE program results were published online in Diabetes Care ahead of print and presented at the 54th European Association for the Study of Diabetes (EASD) Annual Congress in Berlin today. Empagliflozin is currently not approved for use in type 1 diabetes.

Based on the totality of the EASE data, Boehringer Ingelheim has initiated regulatory discussions for empagliflozin as adjunct to insulin for adults with type 1 diabetes.

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