The purpose of this study is to evaluate the safety and cholesterol lowering effects of MPSK3169A when given as subcutaneous (SC) injections over a 24-week period to patients with a high risk of cardiovascular events and LDL-c levels well above goal.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
248
Absolute change from baseline in LDL-c concentration
Time frame: at Day 169
Absolute change from baseline in LDL-c concentration for each arm at the nadir for that arm
Time frame: over the 24 week treatment period
Average value over time of the change in LDL-c (absolute and percent change) for each arm, up to Day 169, weighted by the number of weeks between consecutive LDL-c measurements
Time frame: up to Day 169
Percent change from baseline in LDL-c concentration at Day 169 and at the nadir for each arm
Time frame: at Day 169 and over the 24 week treatment period
Percent and absolute change from baseline in LDL-c concentration at all other designated timepoints
Time frame: at all other designated timepoints
Percent and absolute change from baseline in total cholesterol, non-HDL-c, and apolipoprotein B (ApoB) at Day 169 and at the nadir for each arm
Time frame: at Day 169 and over the 24 week treatment period
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Dose regimen C, repeating subcutaneous injections every 4 weeks
Dose regimen B, repeating subcutaneous injections every 4 weeks
Repeating subcutaneous injections of placebo every 4 weeks
Unnamed facility
Goodyear, Arizona, United States
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Carmichael, California, United States
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Spring Valley, California, United States
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Walnut Creek, California, United States
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Wildomar, California, United States
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Jacksonville, Florida, United States
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Ponte Verde, Florida, United States
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Boise, Idaho, United States
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Indianapolis, Indiana, United States
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Iowa City, Iowa, United States
...and 63 more locations