Overview
Clinical Trial to Evaluate the Effect on the Pharmacokinetic Characteristics of HCP1007 Capsule
Status:
Completed
Completed
Trial end date:
2012-12-01
2012-12-01
Target enrollment:
0
0
Participant gender:
Male
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 1Accepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
Hanmi Pharmaceutical Company LimitedTreatments:
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