A Multicenter Study Comparing the Safety and Efficacy of ABT-335 and Rosuvastatin Calcium Combination Therapy to Monotherapy in Subjects With Dyslipidemia
Completed · Phase 3
Conditions studied: Hypercholesterolemia, Dyslipidemia
In brief
The purpose of this study is to evaluate the safety and efficacy of ABT-335 and rosuvastatin calcium combination therapy to monotherapy in subjects with dyslipidemia.
Key facts
- Study ID
- NCT00463606
- Run by
- AstraZeneca
- People needed
- 760
- Starts
- 2007-04-01
- Expected to finish
- 2008-02-01
- Last updated by the study team
- 2012-10-03
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Adult male and female participants who voluntarily sign the informed consent.
- Fasting lipid results following greater than 12-hour fasting period:
- Triglycerides level greater than or equal to 150 mg/dL,
- High-density lipoprotein cholesterol less than 40 mg/dL for males and less than 50 mg/dL for females, and
- Low-density lipoprotein cholesterol greater than or equal to 130 mg/dL.
- Participant must agree to utilize adequate birth control methods and adhere to the American Heart Association (AHA) diet.
You may not qualify if…
- Participants with unstable medical conditions, medical conditions considered inappropriate in a clinical trial, or participants who are taking excluded concomitant medications are not allowed in the study.
- Participants receiving coumarin anticoagulants or systemic cyclosporine.
Where it is running
- Site Reference ID/Investigator# 4428 — Birmingham, Alabama, United States
- Site Reference ID/Investigator# 4985 — Birmingham, Alabama, United States
- Site Reference ID/Investigator# 4493 — Huntsville, Alabama, United States
- Site Reference ID/Investigator# 4510 — Huntsville, Alabama, United States
- Site Reference ID/Investigator# 4431 — Ozark, Alabama, United States
- Site Reference ID/Investigator# 4519 — Tuscaloosa, Alabama, United States
- Site Reference ID/Investigator# 4395 — Chandler, Arizona, United States
- Site Reference ID/Investigator# 4483 — Gilbert, Arizona, United States
- Site Reference ID/Investigator# 4411 — Scottsdale, Arizona, United States
- Site Reference ID/Investigator# 4417 — Little Rock, Arkansas, United States
- Site Reference ID/Investigator# 4702 — Anaheim, California, United States
- Site Reference ID/Investigator# 5593 — Chula Vista, California, United States
- Site Reference ID/Investigator# 4503 — Concord, California, United States
- Site Reference ID/Investigator# 4530 — Encinitas, California, United States
- Site Reference ID/Investigator# 4458 — Fair Oaks, California, United States
- Site Reference ID/Investigator# 4542 — Fresno, California, United States
- Site Reference ID/Investigator# 4574 — Fresno, California, United States
- Site Reference ID/Investigator# 4441 — Lincoln, California, United States
- Site Reference ID/Investigator# 4432 — Long Beach, California, United States
- Site Reference ID/Investigator# 5579 — Los Angeles, California, United States
- Site Reference ID/Investigator# 4980 — Norwalk, California, United States
- Site Reference ID/Investigator# 4392 — Sacramento, California, United States
- Site Reference ID/Investigator# 4896 — Sacramento, California, United States
- Site Reference ID/Investigator# 5582 — San Diego, California, United States
- Site Reference ID/Investigator# 5469 — Birmingham, Alabama, United States
Full record on ClinicalTrials.gov
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