Safety Study of BMS-770767 in Subjects With Hypercholesterolemia
Completed · Phase 2 · Has a placebo group
Conditions studied: Dyslipidemia
In brief
The purpose of this study is to assess the safety, tolerability and pharmacodynamic effects on LDL cholesterol (LDL-C)
Key facts
- Study ID
- NCT01058083
- Run by
- Bristol-Myers Squibb
- People needed
- 81
- Starts
- 2010-05-01
- Expected to finish
- 2011-03-01
- Last updated by the study team
- 2012-04-19
Who can join
Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Hypercholesterolemia
- Currently taking a stable daily dose of statin therapy
- Serum triglyceride level < 500mg/dl
You may not qualify if…
- History of myocardial infarction, coronary angioplasty or bypass grafts, valvular disease or repair, unstable angina pectoris, transient ischemic attack, or cerebrovascular accidents within six months prior to entry into the study
- Congestive heart failure
- Diabetes mellitus
- Active liver disease
- Impaired renal function
- Hepatitis C, B and HIV
- This list is not inclusive additional information is provided in the protocol
Where it is running
- Harrell, Robert — Little Rock, Arkansas, United States
- Cetero Research - San Antonio — San Antonio, Texas, United States
- Local Institution — Blacktown, New South Wales, Australia
- Local Institution — Hornsby, New South Wales, Australia
- Local Institution — Caboolture, Queensland, Australia
- Local Institution — South Brisbane, Queensland, Australia
- Local Institution — Daw Park, South Australia, Australia
- Local Institution — Nedlands, Western Australia, Australia
- Local Institution — Bathurst, New Brunswick, Canada
- Local Institution — Brampton, Ontario, Canada
- Local Institution — Toronto, Ontario, Canada
- Local Institution — Charlottetown, Prince Edward Island, Canada
- Local Institution — Mirabel, Quebec, Canada
- Local Institution — Montreal, Quebec, Canada
Full record on ClinicalTrials.gov
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