Status:

COMPLETED

Efficacy and Safety of Pioglitazone and Azilsartan in Treating Subjects With Type 2 Diabetes Mellitus

Lead Sponsor:

Takeda

Conditions:

Diabetes Mellitus

Eligibility:

All Genders

18+ years

Phase:

PHASE2

Brief Summary

The purpose of this study is to determine the efficacy of pioglitazone, once daily (QD), combined with azilsartan in the treatment of subjects with Type 2 Diabetes Mellitus.

Detailed Description

Diabetes is a chronic disease with multiple metabolic defects that result in hyperglycemia arising from inadequate insulin activity. Type 2 diabetes has a genetic predisposition, but lifestyle, body c...

Eligibility Criteria

Inclusion

  • Had type 2 diabetes, with a hemoglobin value of greater than or equal to 8.0% or less than 10.0% at Screening.
  • Females of childbearing potential who were sexually active agreed to use adequate contraception, and were neither pregnant nor lactating from Screening throughout the duration of the study.
  • Received antihypertensive therapy and must have been on a stable dose for a minimum of 8 weeks prior to Screening.
  • Had clinical laboratory evaluations (including clinical chemistry, hematology, and complete urinalysis) within the reference range for the testing laboratory unless the results were deemed not clinically significant for inclusion into this study by the investigator or sponsor.
  • Had been on stable diet and exercise program and oral anti-glycemic therapy including sulfonylurea or metformin for 8 weeks prior to Screening.

Exclusion

  • Had a hemoglobin value less than 8.0% or greater than 10.0% at Screening.
  • Was taking an angiotensin II receptor blocker.
  • Had uncontrolled hypertension defined as systolic blood pressure greater than 160 mm Hg and diastolic blood pressure greater than 100 mm Hg. - Had a systolic blood pressure less than or equal to 110 mm Hg and/or diastolic blood pressure less than or equal to 60 mm Hg.
  • Was taking or was expected to take the following medications:
  • antidiabetic agents (other than sulfonylurea or metformin)
  • tricyclic antidepressants
  • monoamine oxidase inhibitors
  • phenothiazines
  • diet medications
  • amphetamines or their derivatives
  • lithium
  • common cold medications with chronic use
  • nonsteroidal anti-inflammatory drugs with chronic use (including aspirin greater than 325 mg/day or cyclooxygenase 2 inhibitors).
  • Had unstable angina or heart failure of any etiology with functional class New York Heart Association III or IV.
  • Had a history of myocardial infarction.
  • Had clinically significant cardiac conduction defects (eg, second or third degree atrioventricular block, left bundle branch block, sick sinus syndrome, atrial fibrillation or flutter).
  • Had secondary hypertension of any etiology (eg, renovascular disease, pheochromocytoma, Cushing's syndrome).
  • Had a history of collagen vascular disorder (eg, systemic lupus erythematosus, scleroderma) within the last 5 years.
  • Had a body mass index greater than 39 kg/m2.
  • Had significant, moderate-to-severe renal dysfunction (creatinine greater than 2.4 mg/dL). If receiving metformin, a creatinine greater than 1.5 mg/dL for male subjects or greater than 1.4 mg/dL for female subjects led to exclusion.
  • Had a history of drug abuse or a history of alcohol abuse within the past 2 years.
  • Had a previous history of cancer, other than basal cell carcinoma, that had not been in remission for at least 5 years prior to the first dose of study drug.
  • Had type 2 diabetes with clinically important retinopathy or peripheral or autonomic neuropathy.
  • Had an alanine aminotransferase or aspartate aminotransferase level of greater than 2.5 times the upper limit of normal, active liver disease, or jaundice.
  • Was participating in another investigational study or had participated in an investigational study within 30 days prior to randomization.
  • Had any other serious disease or condition at Screening (or randomization) that might have compromised subject safety, affected life expectancy, or made it difficult to successfully manage and follow the subject according to the protocol.
  • Was hypersensitive to angiotensin II receptor blockers.
  • Was hypersensitive to thiazolidinediones.

Key Trial Info

Start Date :

July 1 2004

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

October 1 2005

Estimated Enrollment :

704 Patients enrolled

Trial Details

Trial ID

NCT00762736

Start Date

July 1 2004

End Date

October 1 2005

Last Update

February 28 2012

Active Locations (78)

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1

Birmingham, Alabama, United States

2

Huntsville, Alabama, United States

3

Sierra Vista, Arizona, United States

4

Sun City, Arizona, United States