This is a 12-week clinical trial in lipid clinic patients for whom niacin therapy is appropriate to evaluate the efficacy of MK0524 to improve the tolerability of extended-release niacin. There will be 6 scheduled clinic visits and 3 treatment arms.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
825
Global Flushing Severity Score (GFSS) during 7 days of treatment
Time frame: during 7 days of treatment
Percentage of Participants Who Experience at Least 1 Adverse Event
Time frame: up to 10 weeks
Percentage of Participants Who Were Discontinued from the Study Due to an Adverse Event
Time frame: up to 10 weeks
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