Sitagliptin (JANUVIA®)
DrugParticipants prescribed Sitagliptin (JANUVIA®) in routine clinical practice.
NCT Number: NCT01354990
The primary objective of this study is to obtain safety information on the use of sitagliptin (JANUVIA®) from endocrinologists, diabetologists, internists, and general practitioners.
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Observational
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
mellitus
Participants prescribed Sitagliptin (JANUVIA®) in routine clinical practice.
Time frame: Up to approximately 28 months
Time frame: Up to approximately 28 months
Time frame: Up to approximately 28 months
Time frame: Up to approximately 28 months
Merck Sharp & Dohme LLC
Industry
Sitagliptin (JANUVIA®) Post Marketing Surveillance Protocol
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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