Treatment With Bempedoic Acid And/Or Its Fixed-dose Combination With Ezetimibe in Routine Clinical Practice in Patients With Primary Hypercholesterolemia Or Mixed Dyslipidemia
- Sponsor
- Daiichi Sankyo Europe, GmbH, a Daiichi Sankyo Company
- Study ID
- NCT05798390
- Status
- Withdrawn
Conditions
- Mixed Dyslipidemia
- Primary Hypercholesterolemia
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Bempedoic acid and/or its fixed dose combination with ezetimibe — DRUGThis is a non-interventional study. No study medication will be provided as part of this protocol to the patients. Medications will be as prescribed by the treating physician in line with clinical practice.
Study Details
Cardiovascular disease (CVD), especially its management and associated costs, remains a major concern globally. There is a direct correlation between circulating levels of low-density lipoprotein cholesterol (LDL-C) and the incidence of CVD. This study will assess bempedoic acid/FDC in a real-world clinical setting in adult patients in Spain with hypercholesterolaemia or mixed dyslipidemia.
Key Dates
- Start date
- Sep 1, 2023
- Status verified
- Nov 2023
- Primary completion
- Apr 1, 2026
- Completion
- Apr 1, 2026
Study Design
- Enrollment
- 0 participants (actual)
Arms
- Arm: Bempedoic acid and/or fixed-dose combination with ezetimibeParticipants with primary hypercholesterolemia or mixed dyslipidemia who received bempedoic acid and/or its fixed-dose combination with ezetimibe.
Primary Outcome Measure
Summary of Patient Characteristics in Participants With Primary Hypercholesterolaemia or Mixed Dyslipidaemia Following Treatment With Bempedoic Acid And/Or Its Fixed-dose Combination With Ezetimibe [ Time Frame: Baseline up to 12 months ]