Healthy
Conditions
Brief summary
The main objective is to evaluate the food effect on the pharmacokinetic profile of YH4808 100 mg b.i.d and YH4808 300 mg after oral administration in healthy male subjects.
Interventions
DRUGYH4808 100 mg
Period1: YH4808 100 mg bid fasting condition for 7days Period2: YH4808 100 mg bid fed condition for 7days
DRUGYH4808 300 mg
Period1: YH4808 300 mg fasting condition Period2: YH4808 300 mg fed condition(standard meal) Period3: YH4808 300 mg fed condition(high fat meal)
Sponsors
Yuhan Corporation
Study design
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
MALE
Age
20 Years to 45 Years
Healthy volunteers
Yes
Inclusion criteria
* Subjects who signed written consent after receiving thorough explanation on trial purpose, content, and characteristics of investigational drug * Healthy male volunteers in the age between 20 to 45 years old * Weight: over 50kg, within ±20% of ideal body weight * Subjects who were determined to be appropriate through screening
Exclusion criteria
* Clinically significant disorder in liver, kidney, cardiovascular, respiratory system, endocrine system and CNS in the physical examination and clinical laboratory tests or a medical history of malignant tumor or psychological disease * Medical history of gastrointestinal disease or acid restraining surgery, gastric/esophagus surgery (excluding appendectomy, hernia surgery) * A history of hypersensitivity to drugs or clinically significant allergic disease * Clinically significant abnormal values in blood chemistry(≥ 1.5 fold of normal upper limit in the levels of SGOT, SGPT) * Subjects who had a history of drug abuse or who had a positive results on urine drug screening * Subjects who had taken usual dose of any prescription drugs within 14 days before the treatment or who had used usual dose of OTC drugs within 7 days before the treatment(cf, be able to be enrolled in this study according to an investigatory consideration) * Subjects who participated in another clinical trial within 2 months before enrolling in this study * Subjects who donated whole blood within 2 months or component blood within 1 month or who are donated within 1 month before the treatment * Subjects who drank Over 21 units/week of alcohol or subjects who were unable to stop drinking alcohol during the hospitalization * Subjects who stopped smoking within 3 months before the treatment * Subjects who had a beverage containing grapefruits within 24hrs before the hospitalization or who had a beverage containing grapefruits during the hospitalization * Subjects who had a beverage containing caffeine during the hospitalization * Subjects with clinically significant observations considered as unsuitable based on medical judgment by investigators
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Area under the plasma concentration versus time curve of YH4808 | Blood sampling during 24 or 48 hrs after administration | non-compartmental analysis |
| Peak plasma concentration of YH4808 | Blood sampling during 24 or 48 hrs after administration | non-compartmental analysis |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Time to reach peak plasma concentration of YH4808 | Blood sampling during 24 or 48 hrs after administration | non-compartmental analysis |
Countries
South Korea
Outcome results
None listed