Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06295679

A Study Assessing Repatha® in Combination With Standard of Care (SOC) Compared With SOC on Major Cardiovascular Events in Chinese Participants With Atherosclerotic Cardiovascular Disease

A Real-world, Prospective, Observational Study Assessing the Effectiveness of Repatha® Used in Combination With Standard of Care Compared With Standard of Care Alone on Major Cardiovascular Events in Chinese Patients With Established Atherosclerotic Cardiovascular Disease

Status
Recruiting
Phase
Study type
Observational
Enrollment
7,000 (estimated)
Sponsor
Amgen · Industry
Sex
All
Age
18 Years – 150 Years
Healthy volunteers
Not accepted

Summary

The primary objective of the study is to evaluate real-world effectiveness of treatment with Repatha® in combination with SOC, compared with SOC alone, on the risk for cardiovascular (CV) death, myocardial infarction (MI), stroke, hospitalization for unstable angina, or coronary revascularization, whichever occurs first, in participants with established atherosclerotic CV disease (ASCVD) treated with SOC, according to local clinical practice.

Conditions

Timeline

Start date
2022-12-19
Primary completion
2028-12-19
Completion
2028-12-19
First posted
2024-03-06
Last updated
2026-02-20

Locations

90 sites across 1 country: China

Source: ClinicalTrials.gov record NCT06295679. Inclusion in this directory is not an endorsement.

A Study Assessing Repatha® in Combination With Standard of Care (SOC) Compared With SOC on Major Cardiovascular Events i (NCT06295679) · Clinical Trials Directory