Merck Sharp & Dohme Release: Expanded Labelling for Januvia Approved by European Commission

WHITEHOUSE STATION, N.J.--(BUSINESS WIRE)--Jan. 21, 2008--Merck Sharp & Dohme (MSD) today announced that the European Commission has approved 'Januvia' (sitagliptin) for two additional uses for patients with type 2 diabetes. This now makes sitagliptin the only dipeptidyl peptidase-4 inhibitor (DPP-4 inhibitor) approved as an add-on therapy to a sulphonylurea ('dual therapy'), or a sulphonylurea plus metformin ('triple therapy'), in the European Union (EU). It remains the only DPP-4 inhibitor indicated for once-daily use.
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