A Post Marketing Safety Study of Sitagliptin (JANUVIA®) (MK-0431-234)

• Status: Completed
• Trial end date: 2010-05-01
• Target enrollment: 0
• Participant gender: All

Summary

The primary objective of this study is to obtain safety information on the use of sitagliptin (JANUVIA®) from endocrinologists, diabetologists, internists, and general practitioners.

• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Merck Sharp & Dohme Corp.
• Treatments: Sitagliptin Phosphate

Criteria

Inclusion Criteria:

• Must be taking sitagliptin (JANUVIA™) for the treatment of type 2 diabetes

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• Treating physician must agree to provide information regarding the participants treatment