Overview

Investigating the Pharmacokinetic Characteristics of HIP1402 in Healthy Male Volunteers

Status:
Completed
Trial end date:
2015-10-01
Target enrollment:
0
Participant gender:
Male
Summary
To investigate the PK charateristics and the effect of food on the PK in healthy male volunteers who receive HIP1402 capsule 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 19~50 years

2. Weight ≥55kg and ≤90kg, The result of Body Mass Index(BMI) is not less than 18 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. History of relevant drug allergies or clinically significant hypersensitivity
reaction.

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

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

5. 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)

6. Intake of more than 210g of alcohol per week or who can't abstain from alcohol during
the trial.

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

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

9. Subjects who judged ineligible by the investigator.