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Eli Lilly Reports the US FDA’s Acceptance of sNDA for Jardiance to Treat Type 2 Diabetes

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Eli Lilly

Eli Lilly Reports the US FDA’s Acceptance of sNDA for Jardiance to Treat Type 2 Diabetes

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  • The US FDA has accepted an sNDA for Jardiance in children aged ≥10yrs. with T2D. The sNDA was based on the P-III trial (DINAMO) evaluating Jardiance (10/25mg) and Tradjenta (5mg) vs PBO in 175 patients aged 10-17yrs.
  • The results showed a reduction in the 1EPs of change from baseline in A1c @26wks. over PBO. Jardiance (10 & 25mg) pooled doses reduced A1c by 0.84% when added to other baseline treatments, reduction in A1c in patients treated with Tradjenta (linagliptin) was not statistically significant over PBO
  • A numerical reduction of 0.34% was seen & the results were presented during the International Diabetes Federation World Diabetes Congress 2022. The safety data were consistent with the prior known safety profile of Jardiance

Ref: Eli Lilly Image: Eli Lilly

Related News:- NICE Failed to Recommend Boehringer Ingelheim and Lilly’s Jardiance (empagliflozin) for Heart Failure

Click here to­ read the full press release 

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Neha is a Senior Editor at PharmaShots. She is passionate and very enthusiastic about recent updates and developments in the life sciences and pharma industry. She covers Biopharma, MedTech, and Digital health segments along with different reports at PharmaShots. She can be contacted at connect@pharmashots.com.

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