A clinical trial to investigate the pharmacokinetic drug-drug interaction of Cilnidipine 10 mg and Valsartan 160 mg in healthy male volunteers

Not Applicable

Completed

• Conditions: Not Applicable

• Registration Number: KCT0000763
• Lead Sponsor: Ildong pharmaceutical

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: Completed
• Sex: Male
• Target Recruitment: 54

Inclusion Criteria

1) Healthy male volunteers, age 20 to 40 years
2) The result of Body Mass Index(BMI) is not less than 18.5 kg/m2 , no more than 25 kg/m2 and body weight are least 55 kg
3) Subjects who have no congenital or chronic disease and no abnormal symptom or opinion
4) Acceptable serum test, hematologic test, blood chemistry examination, urin test and ECG, physical examination during screening
5) Subjects who have ability to comprehend the objectives, contents of study and property of study drug before participating in trial and have willingness to sign of informed consent in writing

Exclusion Criteria

1) A subject with clinical evidence or history of hepatic (including carrier of hepatitis virus), renal, respiratory, endocrine, neurologic, immunologic, hematologic, oncologic, psychiatric, or cardiovascular disease
2) A subject with a history of gastrointestinal disease or surgery (except simple appendectomy or repair of hernia), which can influence the absorption of the study drug
3) A subject with history of drug allergies (aspirin, antibiotics, including study drug etc.), or history of clinically significant allergies
4) Systolic blood pressure <100mmHg or Diastolic blood pressure < 60 mmHg, systolic blood pressure = 150 mmHg or diastolic blood pressure = 100mmHg(Sitting blood pressure) during the screening procedure.
5) Presence or history of drug abuse or positive result in urine drug screening test
6) Use any prescriptive medication, Korean traditional medication not considered acceptable by the clinical investigator during the last 14 days period before first dosing, or use any OTC medication not considered acceptable by the clinical investigator during the last 7 days period before first dosing (if used medication is considered acceptable by investigator, patients can be included)
7) Participation in clinical trials of any drug within 60 days prior to the participation of the study
8) Blood donation during 2 months or apheresis during 1 month before the study
9) Use of alcohol over 21 units/weeks
10) Smoker who smoke more than 20 cigarettes per day
11) A subject who takes grapefruit, grapefruit juice, or grapefruit-containing products within 3 days prior to the participation of the study
12) A subject who takes St John's wort or some food including the ingredient within 14 days prior to the participation of the study
13) Judged to be inappropriate for the study by the investigator after reviewing clinical laboratory results or other reasons.

Study & Design

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

Primary Outcome Measures

Name	Time	Method
Cmax , AUClast of Cilnidipine 10 mg and Valsartan 160 mg

Secondary Outcome Measures

Name	Time	Method
Tmax, AUCinf, CL/F of Cilnidipine 10 mg and Valsartan 160 mg