Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorDaiichi Sankyo Europe, GmbH, a Daiichi Sankyo Company
About this trial
Data on the real-world use and effectiveness and safety of bempedoic acid combined with both a statin and ezetimibe in clinical practice is limited. There is an increased focus on using combination therapy to lower LDL-C.
Eligibility criteria
Qualifiers
Written informed consent to participate
At least 18 years of age
High and very high risk patients as assessed by the physician suffering from documented primary hypercholesterolemia or mixed dyslipidemia at start of bempedoic acid treatment
bempedoic acid added to ezetimibe and rosuvastatin or atorvastatin,
Disqualifiers
Patients who have received PCSK9i monoclonal antibody treatment in the last 3 months before the start of the triple therapy exposure
Patients who have ever received PCSK9i-siRNA treatment
Trial design
Treatments tested in this trial
- Bempedoic acid
- Ezetimibe
- Rosuvastatin
- Atorvastatin
Treatment groups
2,000 Participants
are divided into 1 treatment groupSponsors and collaborators
Source ClinicalTrials.gov