Efficacy and Safety Study of Pioglitazone Combined With Metformin on Metabolic Syndrome in Subjects With Type 2 Diabetes

Phase

Condition

Hypertriglyceridemia

Metabolic Syndrome

Diabetes And Hypertension

Treatment

N/A

Clinical Study ID

NCT00772174

IT-PIO-108

PIOc/LAN07/TIF

U1111-1115-9278

2006-000725-54

Ages 35-75
All Genders

Study Summary

The purpose of this study was to determine the efficacy of pioglitazone taken with metformin on high-density lipoprotein cholesterol in subjects with Type 2 Diabetes.

Eligibility Criteria

Inclusion

Inclusion Criteria:

Diagnosis of Type 2 Diabetes Mellitus.
Has glycosylated hemoglobin levels between 6.0% and 8.0%.
Treatment with metformin (2,000 to 3,000 mg daily) for at least 3 months.
Has reduced high-density lipoprotein cholesterol levels less than 40 mg/dl in malesand less than 50 mg/dl in females, irrespective of treatment with statins.
Has central obesity defined as a waist circumference greater than or equal to 94 cmfor men and greater than or equal to 80 cm for females.
Females of childbearing potential who are sexually active must agree to use adequatecontraception, and can neither be pregnant nor lactating from Screening throughout theduration of the study.

Exclusion

Exclusion Criteria:

Has a diagnosis of Type 1 Diabetes Mellitus.
Required to take or intends to continue taking any disallowed medication, anyprescription medication, herbal treatment or over-the counter medication that mayinterfere with evaluation of the study medication, including:
other oral antidiabetic drugs than metformin or with insulin in the 3 monthspreceding study entry.
Fibrates
Rifampicin
Has any disease with malabsorption.
Has acute or chronic pancreatitis.
Has familial polyposis coli.
Has a medical history of myocardial infarction, transient ischemic attacks or strokein the past 6 months.
Has heart failure as defined by the New York Heart Association classification I-IV.
Has significant liver impairment, with an alanine aminotransferase level greater than 2.5 the upper limit of normal range.
Has significant renal impairment, with a serum creatinine level greater than 1.5 mg/dlfor men and greater than 1.2 mg/dl for women.
Has anemia of any etiology (defined as hemoglobin levels less than 10.5 g/dL) or anyother hematologic disease.
Has a diagnosis or suspicion of neoplastic disease.
History of chronic alcohol or drug abuse.
Known allergy, sensitivity or intolerance to the study drugs and their formulationingredients.
Participation in another trial in the 3 months preceding study entry.

Study Design

January 01, 2007

February 29, 2008

Study Description

Diabetes is none of the most common, chronic diseases worldwide and affects nearly 200 million people. It is the fourth or fifth leading cause of death in developed countries, and it is expected that diabetes will reach epidemic proportions, affecting 333 million people globally by 2025.

The metabolic syndrome is a cluster of the most dangerous cardiovascular risk factors and includes diabetes and pre-diabetes in addition to abdominal obesity, low high-density lipoprotein cholesterol, high triglycerides and hypertension. It is estimated that around a quarter of the world's adult population has metabolic syndrome, and are twice as likely to die and three times as likely to have a heart attack or stroke when compared to people without the syndrome. In addition, non-diabetic people with metabolic syndrome have a fivefold greater risk of developing type 2 diabetes. The clustering of cardiovascular risk factors that typifies the metabolic syndrome is now considered the driving force for a cardiovascular disease epidemic.

Metabolic syndrome has been recently defined by a Consensus Conference of the International Diabetes Federation as a cluster of clinical and laboratory signs characterized by the presence of abnormal deposition of fat tissue in the abdomen and visceral districts, and at least two other clinical and laboratory abnormalities, including altered glucose metabolism or type 2 diabetes and decreased levels of high-density lipoprotein cholesterol. One of the underlying pathophysiological mechanisms of metabolic syndrome is insulin resistance, characterized by an increased glucose output from the liver, and reduced glucose uptake in the muscle and adipose tissue cells. Drugs whose mechanism of action consists of increasing insulin sensitivity in the target tissues are able to reduce the clinical manifestations and consequences of metabolic syndrome.

While each individual component of metabolic syndrome confers an increased risk of cardiovascular-related complications or death, this risk is more pronounced when the syndrome itself is present. The more components of metabolic syndrome are evident, the higher is the cardiovascular mortality rate.