Dyslipidemia Clinical Trial
Official title:
A Phase 2, Randomized, Double-Blind, Placebo-Controlled Study To Evaluate The Effect Of CP-778,875 On HDL-Cholesterol In Adult Subjects With Dyslipidemia And Type 2 Diabetes Mellitus
Verified date | May 2009 |
Source | Pfizer |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Food and Drug Administration |
Study type | Interventional |
To assess the effect of CP-778,875 on HDL-C cholesterol in adult subjects with dyslipidemia and type 2 diabetes
Status | Completed |
Enrollment | 84 |
Est. completion date | June 2007 |
Est. primary completion date | |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 30 Years to 70 Years |
Eligibility |
Inclusion Criteria: - HDL-C < or = 45 mg/dL for men and < or = 55 mg/dL for women - Triglycerides between 150-500 mg/dL - Fasting Plasma Glucose 140-240 mg/dL Exclusion Criteria: - Known cardiovascular, carotid, or peripheral vascular disease |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
United States | Pfizer Investigational Site | Anniston | Alabama |
United States | Pfizer Investigational Site | Atlanta | Georgia |
United States | Pfizer Investigational Site | Baltimore | Maryland |
United States | Pfizer Investigational Site | Bryan | Texas |
United States | Pfizer Investigational Site | Chicago | Illinois |
United States | Pfizer Investigational Site | Conyers | Georgia |
United States | Pfizer Investigational Site | DeFuniak Springs | Florida |
United States | Pfizer Investigational Site | Destin | Florida |
United States | Pfizer Investigational Site | Greenbrae | California |
United States | Pfizer Investigational Site | Houston | Texas |
United States | Pfizer Investigational Site | Huntsville | Alabama |
United States | Pfizer Investigational Site | Iowa City | Iowa |
United States | Pfizer Investigational Site | Jupiter | Florida |
United States | Pfizer Investigational Site | Kingsport | Tennessee |
United States | Pfizer Investigational Site | Las Vegas | Nevada |
United States | Pfizer Investigational Site | Lexington | Kentucky |
United States | Pfizer Investigational Site | Los Angeles | California |
United States | Pfizer Investigational Site | Melbourne | Florida |
United States | Pfizer Investigational Site | Milwaukee | Wisconsin |
United States | Pfizer Investigational Site | Mount Vernon | New York |
United States | Pfizer Investigational Site | Newport News | Virginia |
United States | Pfizer Investigational Site | Oklahoma City | Oklahoma |
United States | Pfizer Investigational Site | Omaha | Nebraska |
United States | Pfizer Investigational Site | Richmond | Virginia |
United States | Pfizer Investigational Site | Richmond | Virginia |
United States | Pfizer Investigational Site | Richmond | Virginia |
United States | Pfizer Investigational Site | San Antonio | Texas |
United States | Pfizer Investigational Site | Springfield | Missouri |
United States | Pfizer Investigational Site | Tulsa | Oklahoma |
United States | Pfizer Investigational Site | Walnut Creek | California |
United States | Pfizer Investigational Site | Yakima | Washington |
Lead Sponsor | Collaborator |
---|---|
Pfizer |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | HDL-C Safety and Efficacy |
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