A Clinical Trial to Evaluate the Pharmacokinetic Profiles and Safety of CKD-383.

NCT ID: NCT04810676

Last Updated: 2021-06-10

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 27 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-04-16
• Study Completion Date: 2021-05-26

Brief Summary

A clinical trial to evaluate the pharmacokinetic profiles and safety of CKD-383.

Detailed Description

A phase 1 clinical trial to evaluate pharmacokinetics and safety in healthy adult after oral administration of CKD-383 and co-administration of CKD-501, D745, D150.

Conditions

Type2 Diabetes Mellitus

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Sequence 1

Peroid 1: CKD-501, D745, D150 -PO

Peroid 2: CKD-383- PO

Group Type: EXPERIMENTAL

CKD-501, D745, D150

Intervention Type: DRUG

QD, PO

CKD-383

Intervention Type: DRUG

QD, PO

Sequence 2

Peroid 1: CKD-383- PO

Peroid 2: CKD-501, D745, D150 -PO

Group Type: EXPERIMENTAL

CKD-501, D745, D150

Intervention Type: DRUG

QD, PO

CKD-383

Intervention Type: DRUG

QD, PO

Interventions

CKD-501, D745, D150

QD, PO

Intervention Type: DRUG

CKD-383

QD, PO

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Healthy adult volunteers aged between 19 and 55 years old.

2. Weight ≥ 55kg(men) or ≥50kg(women),

3. Calculated body mass index(BMI) of 18.5 to 27.0kg/m2

• Body Mass Index(BMI) = Weight(kg) / [Height(m)]2

4. Women must meet one of the criteria written in below:

• Menopause (No menstruation for 2 years)
• Sterilization (hysterectomy or Oophorectomy, Tubal ligation etc.)

5. Men agree to contraception and not to donate sperm during the participation of clinical trial.

6. Those who voluntarily decide to participate and agree to comply with the cautions after fully understand of the detailed description of this clinical trial.

Exclusion Criteria

1. Those who have a clinically significant disease or medical history of hepatic-biliary system issues, Renal dysfunction, Neurological disorder, Immunity disorder, Respiratory disorder, Genitourinary system disorder, Digestive system disorder, Endocrine system disorder, Cardiovascular disorder, Blood tumor and/or mental health problems.

2. Those who have signs and symptoms of clinically significant dehydration or who are vulnerable to dehydration by poor oral intake.

3. Those who receive intravenous administration of radioactive iodine contrast agents (for Urography, venous cholangiography, angiography, computed tomography using contrast agents, etc.) within 48hours before the first administration of investigational product.

4. Those who have severe urinary tract infection or have a past medical history of it.

5. Those who have genetic problems such as galactose intolerance, Lapp lactose deficiency or glucose-galactose malabsorption.

6. Those who have past medical history of gastrointestinal disorder(Crohn's disease, ulcerative colitis, etc. except simple appendectomy or hernia surgery), which affect the absorption of drug

7. Those who have history of hypersensitivity to active pharmaceutical ingredient(Lobeglitazone, Empagliflozin, Metformin) or additives.

8. Those who have the test results written in below:

• AST/ALT > 1.25 times higher than upper normal level
• eGFR(estimated Glomerular Filtration Rate, which is calculated by MDRD) < 60 mL/min/1.73m2
• "positive" or "reactive" test result of Hepatitis B & C, HIV, PRP
• Under 5 min resting condition, systolic blood pressure >150mmHg or <90mmHg, Diastolic blood pressure >100mmHg, or <50mmHg

9. Those who have a drug abuse history within one year or positive reaction on urine drug screening test

10. Those who received following drugs, which may affect results of clinical trial and safety. Ethical-the-counter (ETC) drugs and herbal medicines within 14 days before the first administration of the investigational drug. Over-the-counter (OTC) drugs, health foods and vitamin preparations within 7 days before the first administration of the investigational product.

11. Those who take barbiturate and related (causing induction or inhibition of metabolism) drug within 1 month before the first administration of investigational product

12. Those who exceeding an alcohol and smoke consumption criteria or can't stop smoking, consuming alcohol and caffeine during hospitalization period (Criteria: Caffeine > 5 cups/day, Alcohol > 210 g/week, Smoke > 10 cigarettes/day)

13. Those who took grapefruit before the first administration of investigational product or can't stop taking grapefruit during hospitalization period

14. Those who received investigational product by participating in other clinical trial within 6 months before the first administration of investigational product

15. Those who donated whole blood within 2 months or apheresis within 1 month

16. Those who received transfusion within 1 month

17. Those who are pregnant or breastfeeding

18. Those who are deemed inappropriate to participate in clinical trial by investigators

• Minimum Eligible Age: 19 Years
• Maximum Eligible Age: 55 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Chong Kun Dang Pharmaceutical

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Min-soo Park, MD, PhD.

Role: PRINCIPAL_INVESTIGATOR

Severance Hospital

Locations

Severance Hospital

Seoul, Yonsei-ro, Seodaemun-gu 50-1, South Korea

Countries

South Korea

Other Identifiers

A101_02BE2020

Identifier Type: -

Identifier Source: org_study_id