4.5 Article

Rationale and design of the CLEAR-outcomes trial: Evaluating the effect of bempedoic acid on cardiovascular events in patients with statin intolerance

Journal

AMERICAN HEART JOURNAL
Volume 235, Issue -, Pages 104-112

Publisher

MOSBY-ELSEVIER
DOI: 10.1016/j.ahj.2020.10.060

Keywords

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Funding

  1. National Health and Medical Research Council of Australia
  2. AstraZeneca
  3. Amgen
  4. Anthera
  5. Eli Lilly
  6. Esperion
  7. Novartis
  8. Cerenis
  9. Medicines Company
  10. Resverlogix
  11. InfraReDx
  12. Roche
  13. Sanofi-Regeneron
  14. LipoScience
  15. CSL
  16. Sanofi
  17. Regeneron
  18. Amarin
  19. Stage II Innovations/Renew, Renew
  20. Kowa
  21. Akcea
  22. FH Foundation
  23. GB Life Sciences
  24. Aegerion
  25. Gemphire
  26. Pfizer
  27. Boehringer Ingelheim
  28. Acasti
  29. Boehringer Ingeiheim
  30. Bristol Meyers Squibb
  31. Civi
  32. Ionis
  33. LIB Therapeutics
  34. iVledInunune
  35. Merck
  36. Omthera
  37. NIHR Imperial Biomedical Research Centre
  38. Esperion Therapeutics
  39. Medtronic
  40. MyoKardia
  41. Silence Therapeutics
  42. Takeda
  43. Orexigen

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Bempedoic acid, as a new drug, effectively lowers atherogenic lipoproteins in patients with statin-associated muscle symptoms. The CLEAR Outcomes study will evaluate the impact of Bempedoic acid on the incidence of adverse cardiovascular events in high vascular risk patients.
Background Although statins play a pivotal role in the prevention of atherosclerotic cardiovascular disease, many patients fail to achieve recommended lipid levels due to statin-associated muscle symptoms. Bempedoic acid is an oral prodrug that is activated in the liver and inhibits cholesterol synthesis in hepatocytes, but is not activated in skeletal muscle which has the potential to avoid muscle-related adverse events. Accordingly, this agent effectively lowers atherogenic lipoproteins in patients who experience statin-associated muscle symptoms. However, the effects of bempedoic acid on cardiovascular morbidity and mortality have not been studied. Study design Cholesterol Lowering via Bempedoic acid, an ACL-Inhibiting Regimen (CLEAR) Outcomes is a randomized, double-blind, placebo-controlled clinical trial. Included patients must have all of the following: (i) established atherosclerotic cardiovascular disease or have a high risk of developing atherosclerotic cardiovascular disease, (ii) documented statin intolerance, and (iii) an LDL-C >= 100 mg/dL on maximally-tolerated lipid-lowering therapy. The study randomized 14,014 patients to treatment with bempedoic acid 180 mg daily or matching placebo on a background of guideline-directed medical therapy. The primary outcome is a composite of the time to first cardiovascular death, nonfatal myocardial infarction, nonfatal stroke, or coronary revascularization. The trial will continue until 1620 patients experience a primary endpoint, with a minimum of 810 hard ischemic events (cardiovascular death, nonfatal myocardial infarction or nonfatal stroke) and minimum treatment duration of 36 months and a projected median treatment exposure of 42 months. Conclusions CLEAR Outcomes will determine whether bempedoic acid 180 mg daily reduces the incidence of adverse cardiovascular events in high vascular risk patients with documented statin intolerance and elevated LDL-C levels.

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