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

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT00521820
Recruitment Status : Terminated (Higher incidence of hospitalization for congestive heart failure in pioglitazone-treated subjects compared to glyburide treated subjects.)
First Posted : August 28, 2007
Last Update Posted : February 28, 2012
Information provided by (Responsible Party):

Brief 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

Condition or disease Intervention/treatment Phase
Diabetes Mellitus Drug: Pioglitazone Drug: Glyburide Phase 3

Detailed Description:

Approximately 16 million people in the United States have been diagnosed with type 2 diabetes, a prevalence rate of approximately 6%, and the numbers are expected to increase with the increasing age of the general population. The risk factors associated with development of type 2 diabetes, such as age, obesity, and diet and exercise habits, also contribute to the development of cardiovascular disease. Additionally, patients with diabetes are at an increased risk for development of microvascular and macrovascular disease.

With regard to congestive heart failure, the risk of congestive heart failure is increased in subjects with diabetes in the absence of coronary artery disease; in subjects with diabetes and established coronary artery disease there is a higher overall risk and greater risk for more severe congestive heart failure. There is evidence that increasing insulin sensitivity and reducing hyperinsulinemia may reduce cardiovascular risks by reducing blood pressure, improving endothelial function, and through cardiac remodeling and function.

Pioglitazone is a thiazolidinedione for the treatment of type 2 diabetes, and is an agonist of the peroxisome proliferator-activated receptor. Pioglitazone received marketing approval in the United States in 1999. As part of the approval process, Takeda fulfilled a postmarketing study evaluating the effects of pioglitazone in the treatment of type 2 diabetes in subjects with congestive heart failure in a6-month clinical study.

An independent Data Safety Monitoring Board used to monitor the overall safety pattern of the study and to conduct unblinded reviews of data found a difference in the composite endpoint of time to first event that approached nominal statistical significance in favor of glyburide. As a result, the committee recommended that Takeda terminate the trial. Consistent with regulatory agency requirements, Takeda is submitting an abbreviated report that focuses on the safety data derived from the terminated study.

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 518 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Official Title: A Randomized, Double-Blind, Comparator-Controlled Study of Pioglitazone HCl vs Glyburide in the Treatment of Subjects With Type 2 (Non-Insulin Dependent) Diabetes Mellitus and Mild to Moderate Congestive Heart Failure
Study Start Date : June 2000
Actual Primary Completion Date : October 2003
Actual Study Completion Date : October 2003

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Heart Failure

Arm Intervention/treatment
Experimental: Pioglitazone QD Drug: Pioglitazone
Pioglitazone 30 mg (titrated to 45mg with tolerance), tablets, orally once daily and glyburide placebo-matching tablets, orally, once daily for up to 24 weeks.
Other Names:
  • Actos
  • AD-4833

Active Comparator: Glyburide QD Drug: Glyburide
Pioglitazone placebo-matching tablets, orally, once daily and glyburide 10 mg (titrated to 15mg with tolerance), capsules, orally, once daily for up to 24 weeks.

Primary Outcome Measures :
  1. Progression of Congestive Heart Failure. [ Time Frame: At First Event. ]

Secondary Outcome Measures :
  1. Change from baseline in Glycosylated Hemoglobin. [ Time Frame: Weeks 12, 20 and Final Visit. ]
  2. Change from baseline in Fasting Plasma Glucose. [ Time Frame: At All Visits. ]
  3. Change from baseline in Triglycerides. [ Time Frame: Weeks 8, 16 and Final Visit. ]
  4. Change from baseline in cholesterol (total cholesterol, high-density lipoprotein and low-density lipoprotein). [ Time Frame: Weeks 8, 16 and Final Visit. ]
  5. Change from baseline in 6 Minute Walking test distance [ Time Frame: At Final Visit ]
  6. Physician & Subject Congestive Heart Failure Global Assessment Score [ Time Frame: At Final Visit ]
  7. Change in New York Heart Association classification [ Time Frame: At All Visits. ]
  8. Minnesota Living with Heart Failure Questionnaire total score. [ Time Frame: At Final Visit. ]
  9. Changes in blood pressure and heart rate. [ Time Frame: At All Visits. ]
  10. All cause mortality. [ Time Frame: At First Event. ]

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

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.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT00521820

Sponsors and Collaborators
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Study Director: VP Clinical Science Strategy Takeda Global Research and Developmnet Center Inc

Additional Information:
Publications of Results:
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Responsible Party: Takeda Identifier: NCT00521820     History of Changes
Other Study ID Numbers: 01-00-TL-OPI-504
U1111-1114-1029 ( Registry Identifier: WHO )
First Posted: August 28, 2007    Key Record Dates
Last Update Posted: February 28, 2012
Last Verified: February 2012

Keywords provided by Takeda:
Glucose Metabolism Disorder
Dysmetabolic Syndrome
Type II Diabetes
Diabetes Mellitus, Lipoatrophic
Drug Therapy

Additional relevant MeSH terms:
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Diabetes Mellitus
Heart Failure
Glucose Metabolism Disorders
Metabolic Diseases
Endocrine System Diseases
Heart Diseases
Cardiovascular Diseases
Hypoglycemic Agents
Physiological Effects of Drugs