A Study of Bempedoic Acid in Combination With Ezetimibe and Either Rosuvastatin or Atorvastatin in Patients With Primary Hypercholesterolemia or Mixed Dyslipidemia

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 group