Safety, Tolerability, Pharmacokinetics And Pharmacodynamics Study Of PF-06291874 As Oral Monotherapy To Treat Adults With Type 2 Diabetes Mellitus

Completed · Phase 2 · Has a placebo group

Conditions studied: Diabetes Mellitus, Type II

In brief

This study is going to assess the safety and tolerability of PF-06291874 in adults with Type 2 Diabetes Mellitus as monotherapy, to evaluate the significance of overall glycemic control in these subjects.

Key facts

Study ID

NCT02175121

Run by

Pfizer

People needed

172

Starts

2014-08-01

Expected to finish

2015-03-01

Last updated by the study team

2016-06-15

Who can join

Age: 18 and older, up to 70. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Male subjects and non-childbearing potential female subjects between the ages of 18 and 70 years old.
• Body Mass Index of 18.0 to 45.4 kg/m2; and a total body weight of >50 kg
• HbA1c value at the screening visit meeting once of the following criteria:
• Currently taking acceptable oral antiglycemic drug therapy within 6.5 to 9.5%
• Not currently taking any oral antiglycemic drug therapy within 7 to 10.5%
• Fasting plasma glucose concentrations<270mg/dL at the screening and run-in visit, confirmed by a single repeat, if deemed necessary.
• Subjects must be willing and able to perform self-tests of blood glucose at least 4 times per day, and maintain a diary for the duration of participation in the study; and therefore, subjects must be literate.

You may not qualify if…

• History of Type 1 diabetes mellitus or secondary forms of diabetes
• One or more self-reported hypoglycemic episodes of sever intensity within 3 months of screening; or 2 or more self-reported hypoglycemic episodes of severe intensity within the previous 6 months.
• History of myocardial infarction, unstable angina, arterial revascularization, stroke, New York Heart Association Functional Class II-IV heart failure, or transient ischemic attach within 6 months of screening.
• History or evidence of diabetic complications with significant end organ damage, such as
• Proliferative retinopathy and/or macular edema;
• Diabetic neuropathy complicated by neuropathic ulcers;
• Screening seated systolic blood pressure >160 mm Hg and/or diastolic blood pressure >100 mm Hg after at least a 5 minute seated rest. If the blood pressure exceeds this limit, the blood pressure may be repeated 2 more times following approximately 2 minutes of rest between measurements and the median of the 3 values should be used to determine subject eligibility;
• Male subjects with partners currently pregnant; or male subjects capable of conceiving children who are unwilling or unable to use a highly effective method of contraception as outlined in this protocol for the duration of the study and for at least 28 days after the last dose of investigational product.

Where it is running

• Anaheim Clinical Trials, LLC — Anaheim, California, United States
• Profil Institute for Clinical Research, Inc. — Chula Vista, California, United States
• Diablo Clinical Research, Inc. — Walnut Creek, California, United States
• Avail Clinical Research, LLC — DeLand, Florida, United States
• SeaView Research, Inc. — Miami, Florida, United States
• SeaView Research, Inc. — Miami, Florida, United States
• Compass Research, LLC — Orlando, Florida, United States
• Miami Research Associates, Inc. — South Miami, Florida, United States
• MRA Clinical Research, LLC — South Miami, Florida, United States
• MRA Clinical Research — South Miami, Florida, United States
• Louisville Metabolic and Atherosclerosis Research Center — Louisville, Kentucky, United States
• DaVita Clinical Research — Minneapolis, Minnesota, United States
• Clinilabs, Inc. — Eatontown, New Jersey, United States
• PRA International — Marlton, New Jersey, United States
• Buffalo Clinical Research Center, LLC — Buffalo, New York, United States
• High Point Clinical Trials Center, LLC — High Point, North Carolina, United States
• Community Research — Cincinnati, Ohio, United States
• Clinical Trials of Texas, Inc. — San Antonio, Texas, United States
• Rainier Clinical Research Center, Inc. — Renton, Washington, United States

Full record on ClinicalTrials.gov

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