A Clinical Study to Evaluate the Pharmacokinetics and Safety of CKD-396

Phase 1

• Conditions: Type2 Diabetes Mellitus
• Interventions: Drug: CKD-501 and D759; Drug: CKD-396

• Registration Number: NCT04246190
• Lead Sponsor: Chong Kun Dang Pharmaceutical

Brief Summary

The purpose of this study is to evaluate the pharmacokinetics and safety of CKD-396.

Detailed Description

Randomized, Open-label, Single-dose, Two-way Crossover Clinical Trial to Investigate the Pharmacokinetics and Safety After Oral Administration of CKD-396 and Co-administration of CKD-501 and D759 in Healthy Adults

Study Timeline

• Status Verified: 2020-01
• Study First Submitted: 2020-01-28
• Study First Submitted QC: 2020-01-28
• Study First Posted: 2020-01-29
• Last Update Submitted: 2020-01-30
• Last Update Posted: 2020-02-05
• Study Start: 2020-02-24
• Primary Completion: 2020-04-10
• Study Completion: 2020-07-16

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 26

Inclusion Criteria

1. Healthy adult who is 19 ~ 55 years at the time of screening
2. Body weight more than 55 kg for male and more than 50kg for female
3. BMI more than 18.5 kg/m2 or less than 27.0 kg/m2
4. Females must be menopause or surgical infertility
5. Males who have consented to the use of appropriate pregnancy contraceptive methods up to 28 days after the last investigational product and not to provide sperm
6. Subjects who voluntarily decided to participate and informed consent based upon understanding on the study.

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Exclusion Criteria

1. Subjects who have a history of clinically significant hepatic, renal, nervous, immune, respiratory, urinary, digestion, endocrine, hematooncology, cardiovascular systemic disease or psychosis disorder

2. Subjects who have diabetic ketoacidoisis, diabetic coma, diabetic precoma, Type 1 diabetes

3. Subjects who have genetic problems such as galactose intolerance, Lapp lactase deficiency or glucose-galactose malabsorption

4. Subjects who have a history of gastrointestinal disorders (Crohn's disease, ulcerative colitis, etc.) or surgery (except simple appendectomy or hernia surgery) that may affect the absorption of the drug

5. Subjects who have a history of clinically significant hypersensitivity to drugs or additives, including components of the investigational product(lobeglitazone, sitagliptin) and same class drug with thiazolidinediones

6. Subjects who have severe infectious disease and severe trauma before and after operation

7. Subjects who are deemed unsuitable as subjects in the screening test performed within 28 days before the administration of investigational product

   • AST, ALT> UNL(Upper Normal Limit)x1.25
   • Total bilirubin > UNL(Upper Normal Limit)x1.5
   • eGFR (Estimated Glomerular Filtration Rate) <60 mL/min/1.73m2 using the MDRD (Modification of Diet in Renal Disease) formula
   • Positive immunologic serological tests (hepatitis B test, hepatitis C test, human immunodeficiency virus (HIV) test, syphilis test)
   • After resting for more than 5 minutes, systolic blood pressure> 150 mmHg or < 90 mmHg, diastolic blood pressure> 100 mmHg or <50 mmHg

8. Subjects who have had a history of drug abuse within one year of screening or have tested positive on urine drug screening test

9. Pregnant or lactating women

10. Subjects who have consistently excessively smoked or consumed caffeine or alcohol (caffeine:> 5 cups / day, alcohol:> 210 g / week, cigarettes:> 10 cigarettes / day) or cannot stop smoking, consuming caffeine and alcohol during hospitalization

11. Subjects who judged to able to affect in the study or in the subject's safety by the investigator for the following reasons

    • Ethical-the-counter (ETC) drugs and herbal medicines within 14 days of the first administration of the investigational drug.
    • Over-the-counter (OTC) drugs, including health foods and vitamin preparations, within 7 days of the first dose of the investigational product

12. Subjects who have received the investigational product by participating in other clinical trials (including bioequivalence studies) within 180 days before the first dose of the investigational product (For biological agents, this may be based on a longer period of time, considering the half-life)

13. Subjects who donated whole blood within 60 days before the first dose of the investigational product or donated component blood donation within 30 days

14. Subjects who received a blood transfusion within 60 days before the first dose of the investigational product

15. Subjects who were deemed to be inappropriate to participate in the study by the investigator judgment

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: CROSSOVER

Arm && Interventions

Group	Intervention	Description
Group 2	CKD-396	* Period 1: CKD-396 * Period 2: CKD-501 and D759
Group 1	CKD-501 and D759	* Period 1: CKD-501 and D759 * Period 2: CKD-396
Group 1	CKD-396	* Period 1: CKD-501 and D759 * Period 2: CKD-396
Group 2	CKD-501 and D759	* Period 1: CKD-396 * Period 2: CKD-501 and D759

Primary Outcome Measures

Name	Time	Method
Cmax of CKD-501, D759 and CKD-396	0(predose)~48 hours	Maximum plasma concentration of CKD-501, D759 and CKD-396
AUClast of CKD-501, D759 and CKD-396	0(predose)~48 hours	Area under the plasma concentration-time curve to last concentration of CKD-501, D759 and CKD-396

Trial Locations

Locations (1)

Yonsei University Severance Hospital; 🇰🇷 Soeul, Korea, Republic of