An Evaluation of Glycemic Control Effects of Mono Therapy CKD-501 in Patients With Type 2 Diabetes Mellitus

Chong Kun Dang

Status and phase

Completed

Phase 3

Conditions

Diabetes Mellitus, Type 2

Treatments

Drug: CKD-501 0.5mg

Drug: Placebo

Study type

Interventional

Funder types

Industry

Identifiers

NCT01001611

19DM09B

CKD-19DM09B

Details and patient eligibility

About

The purpose of this study is to evaluate and confirm hypoglycemic efficacy and safety of CKD-501 as mono therapy in patients with type 2 diabetes treated once daily for 24 weeks in comparison to placebo.

Full description

Diabetes Mellitus is classified into type 1 diabetes and type 2 diabetes mellitus according to the causes of diabetes onset and the treatment of symptoms.

In type 2 diabetes, the combination of insulin resistance and insulin deficiency is working. Diabetes mellitus causing many complications and hospitalization is one of chronic metabolic disorder and diabetes mortality rate has been gradually increasing percentage.

CKD-501 is highly selective peroxisome proliferator-activated receptor-gamma agonist that decreases insulin resistance in the periphery and liver resulting in increased insulin-dependent glucose disposal and decreased hepatic glucose output. In vivo, It demonstrates that CKD-501 improves even more glycemic and lipid control in comparison to rosiglitazone and pioglitazone.

The aim of this phase 3 study was to evaluate the efficacy and safety of CKD-501 once daily for 24 weeks as a monotherapy in type 2 diabetes mellitus. Furthermore, the extension study for additional 28 weeks is designed to confirm long term safety of CKD-501 as an oral hypoglycemic agent.

Enrollment

173 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Type Ⅱ diabetes mellitus
Between 18 years and 80 years old
The patient who has been taking oral hypoglycemic agent since 3 months with HbA1c 6.5 to 9% at screening test or who is drug naive or stopped taking oral hypoglycemic agent more then 3 months with HbA1c 7 to 10% at screening test
BMI between 21kg/㎡ and 40kg/㎡
Diagnosis of type Ⅱ diabetes before 3 months
C-peptide level is over 1.0 ng/ml
Condition for female having contraception methods, surgical sterilization or menopause
Condition for male agreeing to use of recommendatory and appropriate contraception method
Agreement with written informed consent

Exclusion criteria

Type I diabetes, gestational diabetes or secondary diabetes
Treatment with insulin or thiazolidinediones within 60 days
Fasting Plasma Glucose level is over 250 mg/dl
Triglyceride level is 500 mg/dl and over
Uncontrollable hypertension(Although treat with antihypertension agent, systolic blood pressure greater than 140 mmHg and diastolic blood pressure greater than 90 mmHg)
History of myocardial infarction, heart failure, cerebral infarction, hematencephalon or unstable angina within 6 months
Severe hepatic dysfunction: AST, ALT, Total bilirubin, ALP level over or equal to 2.5 times as high as upper normal limit(UNL)
Severe renal dysfunction: Renal failure or serum creatinine greater than 30% normal limit
Anemia for any reason
Needs treatment for acute disease, uncontrolled other diseae or diabetic complications
Abnormality of thyroid function(out of normal TSH range )
History of proliferative diabetic retinopathy
In treatment concomitant drug having severe risk drug interaction with investigational drug
History of cancer within 5 years
History of drug abuse or alcoholism
Hepatitis B Antigen(HBsAg) test is positive
Treatment systemic or inhalant corticosteroids within 1 month prior to Screening
Patient who have experience such as hypersensitivity reaction, serious adverse event or no effect by treatment with glitazones
Fertile women who not practice contraception with appropriate methods
Pregnant women or nursing mothers
Has a contraindication to treatment investigational drug from the medical and psychogenic side
An impossible one who participates in clinical trial by legal or investigator's decision
Participated in other trial within 4 weeks
Participating in other trial at present