Overview

Single-dose, 2-way Crossover Open Study to Evaluate the Food Effect on the PK of HCP1201 in Healthy Volunteers

Status:
Completed
Trial end date:
2013-07-01
Target enrollment:
0
Participant gender:
Male
Summary
To investigate the effect of food in healthy male volunteers who receive HCP1201 tablet in fed versus fasted condition
Phase:
Phase 1
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Hanmi Pharmaceutical Company Limited
Criteria
Inclusion Criteria:

1. Healthy male volunteer, age 20~55 years

2. The result of Body Mass Index(BMI) is not less than 19 kg/m2 , no more than 27 kg/m2

3. Subject who has the ability to comprehend the study objectives, contents and the
property of the study drug before participating in the trial

4. Subject who has the ability and willingness to participate the whole period of trial

Exclusion Criteria:

1. Presence of medical history or a concurrent disease that may interfere with treatment
and safety assessment or completion of this clinical study, including clinically
significant disorders in kidney, liver, cardiovascular system, respiratory system,
endocrine system, or neuropsychiatric system.

2. Glomerular filtration rate is under 60ml/min which is calculated by serum creatinine
value.

3. Liver enzyme (AST, ALT) level exceeds the maximum normal range more than one and a
half times.

4. Systolic Blood Pressure: lower than 90mmHg or higher than 150mmHg, Diastolic Blood
Pressure: lower than 60mmHg or higher than 100mmHg

5. History of relevant drug allergies or clinically significant hypersensitivity
reaction.

6. History of drug abuse or positive drug screening.

7. Participation in other drug studies within 60days prior to the drug administration.

8. Whole blood donation within 60 days, blood component donation within 30 days or who
got transfusion within 30days.

9. Subjects who took prescription drugs within 14 days from the patient screening or
non-prescription medicine within 7 days which can affect the result of this clinical
trial (acceptable according to the investigator's judgement)

10. Subjects who took medicines(e.g. proton pump inhibitor, rifampicin, oriental
medicines, etc.) within 30days that can affect absorption, distribution, metabolism,
elimination of metformin/rosuvastatin.

11. Intake of more than 140g of alcohol per week or who can't abstain from alcohol during
the trial.

12. Subjects who smoke more than 10 cigarettes per day or who can't quit smoking during
the trial.

13. Positive screening on Hepatitis B surface antigen(HBsAg), anti-Hepatitis C virus(HCV)
or anti-Human immunodeficiency virus(HIV).

14. Genetic myopathic disorder or related family history, medical history of myopathic
disorder caused by medication.

15. Clinically inappropriate laboratory test result.

16. Clinically inappropriate electrocardiogram result.

17. Subjects who judged ineligible by the investigator.