US FDA reviewers question Novo Nordisk's IDegLira for type 2 diabetes

23 May 2016

A US Food and Drug Administration (FDA) advisory panel briefing document has questioned the effectiveness of IDegLira, Novo Nordisk’s (NOV: N) insulin degludec (IDeg) Tresiba and liraglutide (Victoza) treatment for type 2 diabetes mellitus (T2DM).

The Danish diabetes giant had the therapy approved in Europe, under the name Xultophy, but it will now be anxiously awaiting the outcome of Tuesday’s advisory panel meeting.

Tresiba and Victoza have both received US FDA approval, and IDegLira has been developed by Novo Nordisk to provide the combined benefits of the two components in a single daily injection.

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