Clinical Study to Evaluate the Pharmacokinetics, Safety and Tolerability of CKD-388 in Healthy Subjects

NCT ID: NCT04676893

Last Updated: 2020-12-21

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE1
• Total Enrollment: 56 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-02-26
• Study Completion Date: 2021-05-18

Brief Summary

This study is an open-label, randomized, single dose, crossover study to evaluate the pharmacokinetics, safety and tolerability of CKD-388 in healthy subjects

Detailed Description

To healthy subjects of fifty-six (56), following treatments are administered dosing in each period and wash-out period is a minimum of 14 days.

Reference drug: D418 Tab. / Test drug: CKD-388 Tab. Pharmacokinetic blood samples are collected up to 72hrs. The pharmacokinetic characteristics and safety are assessed.

Conditions

Chronic Hepatitis b

Study Design

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

Study Groups

Reference-Test

Group Type: EXPERIMENTAL

D418 Tab.

Intervention Type: DRUG

1T

CKD-388 Tab.

Intervention Type: DRUG

1T

Test-Reference

Group Type: EXPERIMENTAL

D418 Tab.

Intervention Type: DRUG

1T

CKD-388 Tab.

Intervention Type: DRUG

1T

Interventions

D418 Tab.

1T

Intervention Type: DRUG

CKD-388 Tab.

1T

Intervention Type: DRUG

Other Intervention Names

Reference; Test

Eligibility Criteria

Inclusion Criteria

1. Healthy male volunteers, aged between ≥ 19 and ≤ 45 years old at the time of screening.

2. Weight ≥ 50kg, with calculated body mass index (BMI) of ≥ 18.5 and ≤ 29.9 kg/m2

• BMI = Weight(kg)/ Height(m)2

3. Individuals who agreed proper contraception during the study and did consent to not donation of sperm 1 month after the last dose of Investigational Product (IP) administration

4. Individuals who voluntary decide to participate and agrees in writing to comply with the precautions after hearing and fully understanding the detailed explanation of this clinical tail

Exclusion Criteria

1. History or presence of clinically significant and sever active cardiovascular, respiratory, hepatobiliary, renal, hematological, gastrointestinal, endocrine, immune, dermatologic, neurologic, or psychiatric disorder.

2. With symptoms indicating acute illness within 28 days prior to the first Investigational Product (IP) administration.

3. Any medical history that may affect drug absorption, distribution, metabolism and excretion.

4. Individuals who had history of hypersensitivity to follow drugs, derivative drugs or others drugs(aspirin and antibiotics etc.) or had history of drug abuse

• Thiazolidinedione
• DPP-4 inhibitor
• Metformin

5. Any clinically significant chronic medical illness.

6. Any genetic disease including galactose intolerance, Lapp lactase deficiency or glucose-galactose malabsorption.

7. Individuals with one of the following laboratory test results in screening

• AST, ALT > UNL (upper normal limit) x 3
• Creatinine clearance ≤ 80 mL/min
• In ECG result, QTc > 450 msec
• hCG(+) (only women)

8. Individuals who had positive test results at HBs Ag, anti-HCV Ab, anti-HIV Ab, VDRL.

9. Use of any prescription drugs within 14 days prior to study drug administration.

10. Use of over-the-counter medications and herbal preparations within 7 days prior to study drug administration.

11. History of any clinically significant allergic reaction (However, mild allergic rhinitis or allergic dermatitis which do not required medication may be allowed).

12. Individuals who cannot eat standard meal provided from clinical trial center.

13. Donation of blood within 60 days prior to study drug administration or apheresis within 20 days prior to the first IP administration.

14. Individuals who had received a blood transfusion within 30 days prior to study drug administration.

15. Exposure to any investigational drug within 6 months prior to the first IP administration.

16. Individuals taking any drugs inducing or inhibiting drug metabolizing enzymes including barbiturates within 30 days prior to the first IP administration.

17. Individuals who had consumed grapefruit juice > 5cups/day or caffeine > 5cups/day within 30 days prior to the first IP administration or who cannot stopping consume grapefruit juice or caffeine during clinical study.

18. Individuals who had drinking (alcohol > 30 g/day) within 30 days prior to the first IP administration or who cannot stop drinking.

19. Heavy smoking (more than 10 cigarettes/day) within 30 days prior to screening or who cannot quit smoking during clinical study.

20. Pregnant or women who may be pregnant

21. Subjects having been deemed inappropriate for the trial as determined by the investigator.

• Minimum Eligible Age: 19 Years
• Maximum Eligible Age: 45 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Chong Kun Dang Pharmaceutical

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Korea University Anam Hospital

Seoul, , South Korea

Countries

South Korea

Central Contacts

Ji-Young Park, Professor

Role: CONTACT

Phone: +82-2-920-6288

Email: jypark21@korea.ac.kr

Facility Contacts

Ji-Young Park, Professor

Role: primary

Other Identifiers

A99_02BE2002

Identifier Type: -

Identifier Source: org_study_id