Conference Coverage

FDA panel advises approval of semaglutide to lower HbA1c in patients with type 2 diabetes


 

AT AN FDA ADVISORY COMMITTEE MEETING

 

The Food and drug Administration’s Endocrinologic and Metabolic Drugs Advisory Committee (EMDAC) recommended the approval of a once-weekly semaglutide injection for adults with type 2 diabetes mellitus. The vote was 16-0 in favor of approval, with one committee member abstaining.

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The committee based its approval recommendation mainly on data from a global phase 3 clinical trial program known as SUSTAIN (clinical trial number NCT01720446) that included evaluations of cardiovascular outcomes, safety, and efficacy in adults with type 2 diabetes, including some with renal disease and increased cardiovascular risk.

The researchers found some increase in diabetic retinopathy in the SUSTAIN trials, but a post-hoc analysis found that “To the extent that the data suggest a signal that there was progression of diabetic retinopathy in patients with significant decreases in HbA1c, these events should be expected because they are consistent with treatments that decrease HbA1c. While this decrease may result in an initial increase in retinopathy, ocular health is ultimately benefited by decreasing HbA1c.”

Novo Nordisk submitted the application for semaglutide in December 2016; the drug also is being reviewed in Europe and Japan.

The FDA is not obligated to follow the committee’s recommendation but considers it as part of the review process of new drug applications.  

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