MPSK3169A
DrugDose regimen A, repeating subcutaneous injections every 4 weeks
NCT Number: NCT01609140
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.
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Notify Me18 year–80 year
All sexes
Interventional
Phase 2
Mount Pearl, Newfoundland and Labrador, Canada
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
And at least one of the following:
Exclusion criteria
The above list is not intended to contain all factors relevant to a patient's eligibility for the study.
Dose regimen A, repeating subcutaneous injections every 4 weeks
Repeating subcutaneous injections of placebo every 4 weeks
Time frame: at Day 169
Time frame: over the 24 week treatment period
Time frame: up to Day 169
Time frame: at Day 169 and over the 24 week treatment period
Time frame: at all other designated timepoints
Time frame: at Day 169 and over the 24 week treatment period
Genentech, Inc.
Industry
A Phase II, Randomized, Placebo-Controlled, Double-Blind Study of the Safety and Efficacy of MPSK3169A in Patients With Coronary Heart Disease or High Risk of Coronary Heart Disease
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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