Overview

PK and Safety of HCP1303 and Co-administration of HGP1201, HIP1402 Under Fed Condition in Healthy Male Volunteers

Status:
Completed
Trial end date:
2015-11-01
Target enrollment:
0
Participant gender:
Male
Summary
To investigate the pharmacokinetic properties and safety after administration of HCP1303 and co-administration of HGP1201, HIP1402 under Fed Condition in healthy male volunteers
Phase:
Phase 1
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Hanmi Pharmaceutical Company Limited
Criteria
Inclusion Criteria:

1. Healthy male volunteer, age 19~55 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. History of relevant drug allergies or clinically significant hypersensitivity
reaction.

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

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

5. SBP: lower than 90mmHg or higher than 150mmHg, DBP: lower than 60mmHg or higher than
100mmHg

6. Subjects who judged ineligible by the investigator.