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Therapeutic Areas: Endocrinology | Family Medicine
 Disease Category: Diabetes Mellitus, Type 2
Location: United States, ND

Trial Information

Type 2 Diabetes and Acute Coronary Syndrome

A study to evaluate cardiovascular outcomes following treatment with Alogliptin in addition to standard of care in subjects with Type 2 Diabetes and Acute Coronary Syndrome.

Patient Inclusion Criteria:

  • Men and women with a diagnosis of T2DM who either are receiving monotherapy or combination antidiabetic therapy.
  • Patients must have an HbA1c level between 7.0% and 10.0%, inclusive, at screening.
  • Patients must have a diagnosis of ACS within 15 to 60 days prior to randomization.

Patient Exclusion Criteria:

  • Signs of Type 1 Diabetes Mellitus including any history of ketoacidosis or requirements for insulin with in 1 year of first diagnosis of diabetes mellitus.
  • Patient is currently receiving a GLP-1 analogue for glycemic control of T2DM at screening.
  • Patient has received a DPP-4 inhibitor for either more than 14 days total or within the 3 months prior to screening.
  • Patient has had an ACS event less than 15 days prior to randomization.

Dr. Thomas Davis, Director
Legacy Pharma Research
601 N. 5th St.
Bismarck, ND 58501
Phone: 701-255-6685
Fax: 701-751-1131
Email: tdavis.legacy@midconetwork.com

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Research Center Information: Legacy Pharma Research

If you would like to learn more about participating in this study, please send an email message using the form below.

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