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| Sponsored by: |
Kos Pharmaceuticals |
| Information provided by: | Kos Pharmaceuticals |
| ClinicalTrials.gov Identifier: | NCT00062556 |
Purpose
The purpose of this study is to evaluate if Niacin ER/Lovastatin, at two different doses, compared to diet control (this group will receive a tablet containing 50 mg. of immediate-release niacin) is a safe and effective medicine in subjects with leg pain caused by a narrowing of their leg arteries, a condition called intermittent claudication.
At least 366 subjects with leg pain caused by a narrowing of their leg arteries will participate in this study.
Niacin ER/Lovastatin is a combination of two FDA (United States Food and Drug Administration) approved cholesterol modifying medications: Niaspan® (extended-release niacin) and lovastatin, a statin (the same medicine found in Mevacor®). Niacin ER/Lovastatin was approved by the FDA under the name of Advicor® for use in the treatment of elevated cholesterol. The use of Niacin ER/Lovastatin in the treatment of peripheral arterial disease and symptomatic relief of intermittent claudication is considered investigational. An investigational use is one that is not approved by the FDA.
| Condition | Intervention | Phase |
|
Intermittent Claudication Peripheral Vascular Disease |
Drug: Niacin Extended Release and Lovastatin Tablets |
Phase III |
| MedlinePlus related topics: | Cholesterol Peripheral Arterial Disease Vascular Diseases |
| Drug Information available for: | Niacin Niacin hydrochloride Lovastatin |
| Study Type: | Interventional |
| Study Design: | Treatment, Randomized, Double-Blind, Dose Comparison, Parallel Assignment, Safety/Efficacy Study |
| Official Title: | Effect of Niacin ER/Lovastatin on Peak Walking Time and Claudication Onset Time in Patients With Intermittent Claudication |
| Estimated Enrollment: | 366 |
| Study Start Date: | January 2003 |
| Estimated Study Completion Date: | March 2006 |
This is a Phase 3, 28-week, double-blind, diet-intervention, randomized, parallel group, three-arm, multi-center, dose-titration study.
The objectives of this study are to evaluate the safety and efficacy of NL in patients with IC. The primary efficacy analysis will be the percent change from baseline in Peak Walking Time (PWT) and Claudication Onset Time (COT), calculated as the logarithm of the quotient of the time walked on treadmill at a visit divided by the time walked at baseline. Other efficacy measures will include Ankle Brachial Index (ABI), QoL measurements, composite of cardiovascular events (MI, stroke, vascular death, and lower limb amputations), and coronary and peripheral artery revascularization procedures. Safety variables will include serum transaminases, routine chemistry parameters, hematology, and AEs. Pharmacokinetic analyses will be conducted as well.
Eligibility
| Ages Eligible for Study: | 40 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
INCLUSION CRITERIA:
EXCLUSION CRITERIA:
Contacts and Locations More Information
| Study ID Numbers: | MA-02-010403, ICPOP |
| First Received: | June 9, 2003 |
| Last Updated: | October 31, 2006 |
| ClinicalTrials.gov Identifier: | NCT00062556 |
| Health Authority: | United States: Food and Drug Administration |
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