Hypertension Clinical Trial
Official title:
A Multi-center, Randomized, Double-blind, Parallel-group Phase III Clinical Trial to Evaluate the Efficacy and Safety of DP-R212 Fixed Dose Combination in Patients With Dyslipidemia and Hypertension
Verified date | June 2017 |
Source | Alvogen Korea |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to determine superiority of DP-R212 comparing to each monotherapy in patient with hypertension and primary hypercholesterolemia.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | August 2017 |
Est. primary completion date | July 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 19 Years and older |
Eligibility |
Inclusion Criteria: - Both man and woman who is over 19 years old - Hypertension patient with hypercholesterolemia Exclusion Criteria: - sSBP difference is =20mmHg or sDBP difference is =10mmHg - A history of cardiovascular disease - rhabdomyolysis, myopathy - Hypertension or hypercholesterolemia due to secondary causes - Uncontrolled diabetes - Evidence of hepatic or renal disease |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Alvogen Korea |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Percent change of LDL-Cholesterol | 0, 8 weeks | ||
Primary | Change of mean seated Systolic Blood Pressure | 0, 8 weeks |
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