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Study to Compare the Safety and Pharmacokinetics of CKD-390 Tablet With Viread® Tablet

Primary Purpose

Chronic Hepatitis B

Status
Completed
Phase
Phase 1
Locations
Korea, Republic of
Study Type
Interventional
Intervention
CKD-390
Viread® tablet
Sponsored by
Chong Kun Dang Pharmaceutical
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Hepatitis B focused on measuring Chronic Hepatitis B virus, HIV-1 infection, Healthy Male Volunteer, Tenofovir Disoproxil Fumarate

Eligibility Criteria

19 Years - 45 Years (Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  1. Healthy male volunteer in the age of 19-45
  2. Body weight ≥ 55kg and in the range of calculated Ideal Body Weight ± 20%
  3. Subject without a hereditary problems, chronic disease and morbid symptom
  4. Subject who sign on an informed consent form willingly

Exclusion Criteria:

  1. Clinically significant disease with hepatobiliary, nephrological, gastrointestinal, respiratory, hepato-oncological, endocrine, urogenital, neurologic, psychiatric, musculoskeletal, immune, otorhinolaryngological, cardiovascular system
  2. Gastrointestinal disease(Crohn's disease, ulcer, acute/chronic pancreatitis) or gastrointestinal surgery(except for appendectomy or herniotomy)
  3. Hypersensitivity reaction or clinically significant hypersensitivity reaction in the history of drugs or additives
  4. Galactose intolerance, Lapp lactase deficiency or Glucose-galactose malabsorption
  5. Sitting systolic blood pressure > 140mmHg or < 100mmHg, sitting diastolic blood pressure ≥ 90mmHg or < 60mmHg, pulse ≥ 100 beats per minute
  6. Aspartate aminotransferase, Alanine aminotransferase, Total bilirubin > 2 x upper limit of normal range
  7. Have the result of Creatinine clearance is less than 50mL/min(Cockcroft-Gault equation applicable)
  8. The history of drug abuse or drug abuse showed a positive for urine drug test
  9. Subject treated metabolizing enzyme inducers or inhibitors including barbiturates within 1 month
  10. Subject treated ethical the counter or herbal medicine within 2 weeks, over-the-counter or vitamin within 1 week
  11. Taking drugs have received any other investigational drug within 3 months prior to the first dosing
  12. Whole blood donation within 2 months prior to the first dosing or component blood donation within 1 months prior to the first dosing or blood transfusion within 1 month
  13. Continuously taking excessive alcohol (> 21 units/week; 1 unit = 10g of pure alcohol) or cannot stop drinking from 24 hours before admission to discharge
  14. Cigarette > 10 cigarettes a day on average for recent 3 months
  15. Subjects with planning of dental treatment (tooth extraction, endodontic treatment etc.) and any surgery (aesthetic operation, laser in-situ keratomileusis, laser assisted sub-epithelial keratomileusis etc.) from signed on an informed consent form to post-study visit
  16. An impossible one who participants in clinical trial by investigator's decision including laboratory test result or another reason

Sites / Locations

  • Chungnam National University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Viread® tablet

CKD-390

Arm Description

Tenofovir Disoproxil Fumarate

Tenofovir Disoproxil Fumarate

Outcomes

Primary Outcome Measures

AUCt of Tenofovir

Secondary Outcome Measures

AUCinf
Blood pressure
tmax
t1/2β
Clearance/F
Electrocardiography
Physical Examination
Pulse rate
Temperature

Full Information

First Posted
October 6, 2015
Last Updated
January 11, 2016
Sponsor
Chong Kun Dang Pharmaceutical
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1. Study Identification

Unique Protocol Identification Number
NCT02589457
Brief Title
Study to Compare the Safety and Pharmacokinetics of CKD-390 Tablet With Viread® Tablet
Official Title
A Randomized, Open-label, Single-dosing, 2x2 Crossover Study to Compare the Safety and Pharmacokinetics of CKD-390 Tablet (Tenofovir Disoproxil Aspartate) With Viread® Tablet (Tenofovir Disoproxil Fumarate) in Healthy Male Volunteers
Study Type
Interventional

2. Study Status

Record Verification Date
January 2016
Overall Recruitment Status
Completed
Study Start Date
October 2015 (undefined)
Primary Completion Date
December 2015 (Actual)
Study Completion Date
December 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Chong Kun Dang Pharmaceutical

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to compare the safety and pharmacokinetics of CKD-390(Tenofovir Disoproxil Aspartate) and Viread® tablet(Tenofovir Disoproxil Fumarate) in healthy male volunteers.
Detailed Description
A Randomized, Open-label, Single-dosing, 2x2 Crossover Study to Compare the Safety and Pharmacokinetics of CKD-390 Tablet (Tenofovir Disoproxil Aspartate) With Viread® Tablet (Tenofovir Disoproxil Fumarate) in Healthy Male Volunteers

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Hepatitis B
Keywords
Chronic Hepatitis B virus, HIV-1 infection, Healthy Male Volunteer, Tenofovir Disoproxil Fumarate

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Viread® tablet
Arm Type
Active Comparator
Arm Description
Tenofovir Disoproxil Fumarate
Arm Title
CKD-390
Arm Type
Experimental
Arm Description
Tenofovir Disoproxil Fumarate
Intervention Type
Drug
Intervention Name(s)
CKD-390
Intervention Description
Tenofovir Disoproxil Aspartate 1T PO
Intervention Type
Drug
Intervention Name(s)
Viread® tablet
Intervention Description
Tenofovir Disoproxil Fumarate 1T PO
Primary Outcome Measure Information:
Title
AUCt of Tenofovir
Time Frame
0(Pre-dose) up to 72hr
Secondary Outcome Measure Information:
Title
AUCinf
Time Frame
0(Pre-dose) up to 72hr
Title
Blood pressure
Time Frame
1 day, 2 day, 3 day, 4 day, 15 day 16 day, 17 day 18 day, 25 day
Title
tmax
Time Frame
0(Pre-dose) up to 72hr
Title
t1/2β
Time Frame
0(Pre-dose) up to 72hr
Title
Clearance/F
Time Frame
0(Pre-dose) up to 72hr
Title
Electrocardiography
Time Frame
1 day, 2 day, 3 day, 4 day, 15 day 16 day, 17 day 18 day, 25 day
Title
Physical Examination
Time Frame
1 day, 2 day, 3 day, 4 day, 15 day 16 day, 17 day 18 day, 25 day
Title
Pulse rate
Time Frame
1 day, 2 day, 3 day, 4 day, 15 day 16 day, 17 day 18 day, 25 day
Title
Temperature
Time Frame
1 day, 2 day, 3 day, 4 day, 15 day 16 day, 17 day 18 day, 25 day

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
19 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Healthy male volunteer in the age of 19-45 Body weight ≥ 55kg and in the range of calculated Ideal Body Weight ± 20% Subject without a hereditary problems, chronic disease and morbid symptom Subject who sign on an informed consent form willingly Exclusion Criteria: Clinically significant disease with hepatobiliary, nephrological, gastrointestinal, respiratory, hepato-oncological, endocrine, urogenital, neurologic, psychiatric, musculoskeletal, immune, otorhinolaryngological, cardiovascular system Gastrointestinal disease(Crohn's disease, ulcer, acute/chronic pancreatitis) or gastrointestinal surgery(except for appendectomy or herniotomy) Hypersensitivity reaction or clinically significant hypersensitivity reaction in the history of drugs or additives Galactose intolerance, Lapp lactase deficiency or Glucose-galactose malabsorption Sitting systolic blood pressure > 140mmHg or < 100mmHg, sitting diastolic blood pressure ≥ 90mmHg or < 60mmHg, pulse ≥ 100 beats per minute Aspartate aminotransferase, Alanine aminotransferase, Total bilirubin > 2 x upper limit of normal range Have the result of Creatinine clearance is less than 50mL/min(Cockcroft-Gault equation applicable) The history of drug abuse or drug abuse showed a positive for urine drug test Subject treated metabolizing enzyme inducers or inhibitors including barbiturates within 1 month Subject treated ethical the counter or herbal medicine within 2 weeks, over-the-counter or vitamin within 1 week Taking drugs have received any other investigational drug within 3 months prior to the first dosing Whole blood donation within 2 months prior to the first dosing or component blood donation within 1 months prior to the first dosing or blood transfusion within 1 month Continuously taking excessive alcohol (> 21 units/week; 1 unit = 10g of pure alcohol) or cannot stop drinking from 24 hours before admission to discharge Cigarette > 10 cigarettes a day on average for recent 3 months Subjects with planning of dental treatment (tooth extraction, endodontic treatment etc.) and any surgery (aesthetic operation, laser in-situ keratomileusis, laser assisted sub-epithelial keratomileusis etc.) from signed on an informed consent form to post-study visit An impossible one who participants in clinical trial by investigator's decision including laboratory test result or another reason
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jang Hee Hong, MD, PhD
Organizational Affiliation
Chungnam National University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Chungnam National University Hospital
City
Daejeon
State/Province
Jung-gu
ZIP/Postal Code
301-721
Country
Korea, Republic of

12. IPD Sharing Statement

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Study to Compare the Safety and Pharmacokinetics of CKD-390 Tablet With Viread® Tablet

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