A Study to Determine the Effect of WelChol Tablets on Cholesterol in Patients Who Have Been Taking Pravastatin for at Least 4 Weeks.
Completed · Phase 4 · Has a placebo group
Conditions studied: Hypercholesterolemia
In brief
Determine the effect of WelChol tablets on serum lipids, lipoproteins, apolipoproteins, and lipoprotein particle size in patients who were stabilized on pravastatin therapy for at least 4 weeks.
Key facts
- Study ID
- NCT00755352
- Run by
- Daiichi Sankyo
- People needed
- 67
- Starts
- 2002-11-01
- Expected to finish
- 2005-04-01
- Last updated by the study team
- 2015-04-03
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Male or female > or = to 18 years of age
- On a stable dose of pravastatin
- LDL-C > or = to 100 mg/dL and < or = 250 mg/dL
- Triglycerides < or = to 300 mg/dL
- Women are not pregnant or breast-feeding or planning to become pregnant
- Women have had a hysterectomy or tubal ligation, or who are post-menopausal or who practice an accepted method of birth control as specified in the protocol
You may not qualify if…
- BMI > 40 kg/m2
- History of allergic or toxic reaction to colesevelam HCL
- History of swallowing disorder
- Any serious condition that would interfere with the conduct of the study
Where it is running
- Study site — Los Angeles, California, United States
- Study site — Castle Rock, Colorado, United States
- Study site — Jacksonville, Florida, United States
- Study site — Pembroke Pines, Florida, United States
- Study site — St. Petersburg, Florida, United States
- Study site — Chicago, Illinois, United States
- Study site — Indianapolis, Indiana, United States
- Study site — Louisville, Kentucky, United States
- Study site — Rochester, New York, United States
- Study site — Cincinnati, Ohio, United States
- Study site — Cleveland, Ohio, United States
- Study site — Bartlett, Tennessee, United States
- Study site — Norfolk, Virginia, United States
- Study site — Richmond, Virginia, United States
- Study site — Seattle, Washington, United States
Full record on ClinicalTrials.gov
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