A clinical trial to evaluate the effects of food on the bioavailability of CKD-397 in healthy male subjects

Not Applicable

Active, not recruiting

• Conditions: Diseases of The genitoruinary system

• Registration Number: KCT0001862
• Lead Sponsor: Chong Kun Dang

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 11 March 2019

Recruitment & Eligibility

• Status: Active, not recruiting
• Sex: Male
• Target Recruitment: 16

Inclusion Criteria

1. Healthy male subject older than 19 years at the time of screening.
2. Subjects who BMI more than 17.5kg/m2 and less than 30.5kg/m2 and weight more than 55kg
3. Subjects who signed the informed consent form after understanding fully to hear a detailed explanation in the clinical trial

Exclusion Criteria

1. Subjects who have 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 have 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 or estimated Glomerular Filteration Rate(eGFR) < 60 mL/min/1.73m2
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 =100 or =150 mmHg or Diastolic Blood Pressure =60 or =100 mmHg at screening
7. Subjects who have orthostatic hypotension
8. Subjects who have history of drug abuse or drug abuse positive at screening
9. Subjects who treated with metabolizing enzyme inducers or inhibitors such as barbitals within 30days prior to the first dosing.
10. Smoker ( = 20cigarettes/day)
11. Subjects who takes Ethical The Count(ETC) or herb medicine within two weeks or Over The Count(OTC) or vitamin supplement within 1 week before the first IP administration
12. Subjects who do the whole blood donation within two months or component blood donation within 1month prior to the first dosing or receive blood transfusion within 1month prior to the first dosing
13. 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
14. Subjects who take organic nitrate medicine regularly or intermittently
15. Patients with genetic degenerative retimal disease including retinitis pigmentosa
16. Subjects who have hypersensitivity to medicines including tadalafil/tamsulosin component or any other medicines(aspirin, antibiotics etc.) or medical history of clinically significant hypersensitivity
17. Patients who lost sight of one eye by Non-arteritic anterior ischemic optic neuropathy(NAION)
18. Subjects with hereditary diseases of galactose intolerance, Lapp lactase deficiency or glucose-galactose malabsorption
19. Subjects who use a trustworthy method of contraception
20. Subjects who is not able to comply with guidelines described in the protocol
21. Subjects who is determined by investigator's decision including laboratory test result or another reason as unsuitable for clinical trial participation

Study & Design

• Study Type: Interventional Study
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
AUC0-t, Cmax of Tadalafil and Tamsulosin

Secondary Outcome Measures

Name	Time	Method
AUCinf, Tmax, t1/2, CL/F, Vd/F of Tadalafil and Tamsulosin