A Clinical Study to Compare the Pharmacokinetic Characteristics of CKD-395 0.25/750 mg in Healthy Male Volunteers

Chong Kun Dang

Status and phase: Completed; Phase 1

Conditions: Diabetes Mellitus, Type II

Treatments: Drug: Duvie Tab. 0.5mg, Glucodaun OR Tab. 750mg; Drug: CKD-395 0.25/750mg

Study type: Interventional

Funder types: Industry

Identifiers

NCT02627027

158BE15004

Details and patient eligibility

About

This study is a randomized, open-label, single dose, 2-way crossover study to compare the pharmacokinetic characteristics of CKD-395 0.25/750 mg in healthy male volunteers.

Full description

To healthy male subjects of twenty six(26), following treatments are administered dosing in each period fed condition(high fat meals) and wash-out period is a minimum of 7 days.

Treatment A(Reference Drug): DuvieTM Tab. 0.5mg 1T + Glucodaun OR Tab. 750mg 2T Treatment B(Test Drug): CKD-395 0.25/750mg Tab. 2T Pharmacokinetic blood samples are collected up to 48hrs. Safety and pharmacokinetic are assessed.

Enrollment: 26 patients

Sex: Male

Ages: 19+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

1. Healthy man older than 19 years at the time of screening.
2. BMI more than 17.5kg/m2 and less than 30.5kg/m2 and weight more than 55kg
3. Subject without congenital or chronic diseases and no psychotic symptoms or findings from the medical examination.
4. Suitable subject who is determined by laboratory tests such as hematology tests,blood chemistry, urinalysis test according to the characteristics of the drug and screening tests such as ECG test.
5. Subject who fully understand the clinical trials after in-depth explanation given prior to the clinical study, decided to join the clinical trials by their will and signed consent form which approved by Chonbuk National University Hospital IRB.
6. Subjects who are able to comply with all scheduled visits, laboratory tests and other procedures.

Exclusion criteria

1. Subjects who has a history of blood, kidneys, endocrine, respiratory, gastrointestinal, urinary, cardiovascular, hepatic, psychiatric, neurological or allergic diseases that is clinically significant (Except untreated asymptomatic seasonal allergies at the time of administration)
2. Subjects who has a history of gastrointestinal disease or gastrointestinal surgery which can affect drug absorption.
3. Subjects who show AST or AST > 2 times upper limit of normal range.
4. Subjects who drink Alcohol > 210g/week within 6 months prior to the screening.
5. Subjects who take the medication involved in other clinical trials or bioequivalence tests within three months before the first dose medication characters.
6. Subjects who show Systolic Blood Pressure ≥ 140 mmHg or Diastolic Blood Pressure ≥ 90 mmHg at screening.
7. Subjects who have history of alcohol or drug abuse, within 1 year
8. Subjects who treated with metabolizing enzyme inducers or inhibitors such as barbitals within 30days prior to the first dosing.
9. Smoker ( ≥ 20cigarettes/day)
10. Subjects who takes ETC or OTC medicine within 10days before the first IP administration.
11. Subjects who do the whole blood donation within two months or component blood donation within 1month prior to the first dosing.
12. Subjects who can increase risk due to clinical test and administration of drugs or has Severe grade / chronic medical, mental condition or abnormal laboratory result that may interfere with the analysis of test results.
13. Patients with hypersensitivity to lobeglitazone or any other thiazolidinediones ( Rosiglitazone, Rioglitazone) and to Metformin or any other biguanides
14. Patients with severe heart failure or congestive heart failure of needing drug therapy
15. Patients with liver disease
16. Patients with severe renal disease
17. Patients with diabetes mellitus with ketoacidosis, diabetes coma and prior
18. Patients before or after surgery, with severe infections, severe trauma
19. Subjects with hereditary diseases of galactose intolerance, Lapp lactase deficiency or glucose-galactose malabsorption
20. Patients with renal disease or renal failure caused by cardiovascular collapse, acute myocardial infarction, sepsis (Serum creatinine ≥ 1.5mg/dL or abnormal creatine clearance)
21. Patients who had a test to injecting radioactive iodine in vein
22. Patients with severe infections or severe traumatic whole body injuries
23. Patients with undernourishment condition or starvation state or hyposthenia or hypopituitarism, or hypoadrenalism
24. Patients with respiratory failure, or stomach disease
25. Subjects who is not able to intake high fat meals
26. Subjects who is not able to comply with guidelines described in the protocol.
27. Subjects who is determined by investigator's decision as unsuitable for clinical trial participation.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Crossover Assignment

Masking: None (Open label)

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26 participants in 2 patient groups

RT group

Experimental group

Description:

R: Reference drug(Duvie Tab. 0.5mg 1T, Glucodaun OR Tab. 750mg 2T) T: Test drug(CKD-395 0.25/750 mg 2T)

Treatment:

Drug: CKD-395 0.25/750mg

Drug: Duvie Tab. 0.5mg, Glucodaun OR Tab. 750mg

TR group

Experimental group

Description:

T: Test drug(CKD-395 0.25/750 mg 2T) R: Reference drug(Duvie Tab. 0.5mg 1T, Glucodaun OR Tab. 750mg 2T)

Treatment:

Drug: CKD-395 0.25/750mg

Drug: Duvie Tab. 0.5mg, Glucodaun OR Tab. 750mg