Safety Comparison of Pioglitazone and Glyburide in Type 2 Diabetes Subjects With Mild to Moderate Congestive Heart Failure

• Status: Terminated
• Trial end date: 2003-10-01
• Target enrollment: 0
• Participant gender: All

Summary

The purpose of this study is to compare the safety of Pioglitazone, once daily (QD), to Glyburide in Type 2 Diabetes Subjects with Mild to Moderate Congestive Heart Failure

• Phase: Phase 3
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Takeda
• Treatments: Glyburide; Pioglitazone

Criteria

Inclusion Criteria

• Females of childbearing potential must be using appropriate birth during the entire duration of the study or must be surgically sterile.

• Subjects with a clear diagnosis of type 2 diabetes mellitus using diagnostic criteria of the American Diabetes Association who have been taking a sulfonylurea and/or insulin for at least 30 days prior to Visit 1 or who have been withdrawn from metformin therapy, during the 30 days prior to Visit 1, due to congestive heart failure.

• Subjects with a clinical diagnosis of congestive heart failure, New York Heart Association Class II or early Class III. Subjects should not previously have been in Class IV heart failure.

• Diagnosis of left ventricular congestive heart failure as evidenced by a left ventricular ejection fraction less than 40% at screening based on an echocardiogram.

• Subjects who have demonstrated the need for oral hypoglycemic agents and have participated in dietary counseling.

• Glycosylated hemoglobin greater than 7.0% at screening.

• Subjects on optimal therapy for congestive heart failure. Medication doses should be stable for at least two weeks prior to randomization.

Exclusion Criteria

• Naïve to antidiabetic therapy.

• Within the past three months were treated with rosiglitazone, pioglitazone HCl, or troglitazone or those previously treated with rosiglitazone, pioglitazone HCl, or troglitazone but discontinued from therapy due to lack of efficacy or clinical or laboratory signs of intolerance.

• Type 1 (insulin-dependent) diabetes mellitus or a history of ketoacidosis.

• Has taken any other investigational drug during the 30 days prior to Visit 1 or who will receive such a drug during the timeframe of this study.

• History of chronic alcoholism or drug abuse during the six months prior to the study.

• Has had any of the following within three months prior to Visit 1: myocardial infarction, coronary angioplasty or bypass graft, unstable angina pectoris, transient ischemic attacks, or documented cerebrovascular accident that in the investigator's opinion would warrant exclusion from the study.

• Abdominal, thoracic, or vascular surgery during the three months prior to Visit 1 that in the investigator's opinion would warrant exclusion from the study.

• Subjects with a planned surgical or catheterization intervention within the six months following Visit 1.

• Subjects awaiting cardiac transplantation.

• Intercurrent illness severe enough to require hospitalization during the three weeks prior to Visit 1.

• Body mass index greater than 48 kg/m2 as calculated by [Weight (kg)/Height (m)2].

• Anemia having a hemoglobin less than 10.5 g/dL for males and less than 10 g/dL for females.

• Thyroid stimulating hormone greater than 3.5 mU/L or less than 0.3 mU/L. The thyroid stimulating hormone can be repeated at two months. The subject is eligible if the screening thyroid stimulating hormone is elevated, and the repeat value at two months is less than 3.5 mU/L.

• Triglyceride level greater than 500 mg/dL.

• Clinical evidence of active liver disease or alanine transaminase levels greater than 1.5 times the upper limit of normal.

• Serum creatinine greater than 2.0 mg/dL for males and greater than 1.8 mg/dL for females or urinalysis protein (albumin) excretion greater than 2 plus on Combistix or equivalent (if elevated, may be re-screened in one month).

• Unstable coronary syndromes which in the opinion of the investigator would warrant exclusion from the study.

• Systolic blood pressure of greater than 150 mmHg or diastolic blood pressure greater than 100 mmHg.

• Serious uncontrolled cardiac rhythm disturbances which in the opinion of the investigator would warrant exclusion from the study.

• Symptomatic orthostatic hypotension or systolic blood pressure less than 90 mm/Hg.

• Severe, advanced peripheral vascular disease (limb threatening ischemia) or claudication resulting in the inability to walk greater than 1 block or to climb 10 stairs without interruption.

• Lower extremity amputation.

• Any other serious disease or condition at screening or at randomization which might affect life-expectancy or make it difficult to successfully manage and follow the subjects according to the protocol.

• Unexplained clinically significant findings on chest x-ray.