Overview

Clinical Trial to Evaluate the Effect on the Pharmacokinetic Characteristics of HCP1007 Capsule

Status:
Completed
Trial end date:
2012-12-01
Target enrollment:
0
Participant gender:
Male
Summary
The purpose of this study is to evaluate pharmacokinetics and safety after oral administration of HCP1007 capsules and Rosuvastatin plus Omega-3.
Phase:
Phase 1
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Hanmi Pharmaceutical Company Limited
Treatments:
Rosuvastatin Calcium
Criteria
Inclusion Criteria:

- Healthy male volunteers, age between 20 and 45

- Informed of the investigational nature of this study and voluntarily agree to
participate in this study

- BMI of >20kg/m2 and <26kg/m2 subject

Exclusion Criteria:

- Use of any prescription medication within 14 days prior to Day 1

- Use of any medication within 7 days prior to Day 1

- Participation in another clinical study within 60 days prior to start of study drug
administration