Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Hypercholesterolemia
  • Mixed Dyslipidemia
Type
Observational
Design
Observational Model: CohortTime Perspective: Prospective

Participation Requirements

Age
Between 18 years and 125 years
Gender
Both males and females

Description

This non-interventional study will be conducted to characterize the risks and benefits of bempedoic acid and/or its fixed-dose combination with ezetimibe in a real-world clinical setting in adult patients with hypercholesterolaemia or mixed dyslipidaemia and to gain insight into the effectiveness (m...

This non-interventional study will be conducted to characterize the risks and benefits of bempedoic acid and/or its fixed-dose combination with ezetimibe in a real-world clinical setting in adult patients with hypercholesterolaemia or mixed dyslipidaemia and to gain insight into the effectiveness (managing plasma levels of low-density lipoprotein cholesterol) as well as safety (clinical events associated with the treatment modalities). Real world evidence will be collected in 8000 participants, treated by specialized as well as non-specialized physicians in hospitals and office based centers.

Tracking Information

NCT #
NCT04579367
Collaborators
Not Provided
Investigators
Study Director: Global Clinical Leader Daiichi Sankyo Europe, GmbH, a Daiichi Sankyo Company