niacin extended-release formulation / Generic mfg.  >>  Phase 4
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Trial + Data / EventsStatusPhNRegionInterventionsSponsorConditionsPrimary complStudy compl
niacin extended-release formulation / Generic mfg.
2005-004080-28: Efficacy and Safety of Niaspan in South Asian Stroke Survivors: NIASTAR TRIAL(Niaspan: Indo-Asian Stroke patienT Atherosclerotic Regression trial)

Ongoing
4
280
Europe
Niaspan, Simvastatin, Niaspan, Simvastatin, Niaspan, Simvastatin
Sandwell Medical Research Unit
1. Patients diagnosed as having a stroke based on the WHO CriteriaPatients with transient ischaemic attacks will be included if symptoms of motor or sensory loss were demonstrable with full recovery within 24 hours. Only strokes and TIA that are ischaemic in nature (thrombo-embolic) will be included in the study
 
 
2005-002982-35: The effect of Niaspan (slow release nicotinic acid) on plasma phosphate, and renal phosphate handling in patents with severe chronic kidney disease

Ongoing
4
40
Europe
Niaspan, Phosex, Niaspan, PL 14994/0001, Niaspan, Phosex, Niaspan, Phosex
Barts and The London NHS Trust
Chronic renal failure (CKD stages 4 &%)
 
 
2005-005347-25: Impact of 12 weeks of oral niacin on endothelial function, lipid composition and cardiovascular biomarkers in patients with coronary artery disease: A prospective, randomized, double-blind, placebo-controlled, monocentric clinical trial of phase IV

Ongoing
4
130
Europe
Niaspan, Niaspan
Johannes Gutenberg-Universität Mainz, II. Med. Klinik (ausführende Stelle), Prof. Dr. med. T. Münzel
Women or men > 35 and < 80 years of age with a documented, clinically stable coronary artery disease (CAD) and a flow-mediated vasodilatation (FMD) of less than 8% from the heart catheter register of the department of medicine II, Johannes Gutenberg-University Mainz.
 
 
2007-000197-24: EFFECTS OF NICOTINIC ACID PLUS SIMVASTATIN VS.SIMVASTATIN ALONE ON CAROTID AND FEMORAL INTIMA-MEDIA THICKNESS IN PATIENTS WITH PERIPHERAL ARTERY DISEASE (NASCIT) –A RANDOMIZED CONTROLLED TRIAL

Ongoing
4
200
Europe
Simvastatin Merck 40mg, Niaspan 500mg, Simvastatin Merck 40mg 1-24892, Niaspan 500mg Merck 1-25383, Simvastatin Merck 40mg 1-24892, Niaspan 500mg Merck 1-25383
MUW, Univ.Klinik f. Innere Medizin II, Abteilung f. Angiologie
200 consecutive patients with PAD and low serum HDL cholesterol levels (<45mg/dL in men, <55 mg/dL in women) will be enrolled in this single-center prospective randomized controlled open-label trial.
 
 
2008-000465-37: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, 12-Week Study to Evaluate the Efficacy and Safety of Extended Release (ER) Niacin/Laropiprant When Added to Ongoing Lipid-Modifying Therapy in Dyslipidemic Patients.

 
3/4
200
Europe
MK-0524A (ER-Niacin/Laropiprant) 1g/20mg, MK-0524A (ER-Niacin/Laropiprant) 1g/20mg,
Laboratoires Merck Sharp & Dohme - Chibret, Merck Sharp & Dohme GmbH, Merck Sharp & Dohme de España, S.A., MSD BV
Dyslipidemia
 
07/08

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