Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/53810
Title: Safety and efficacy of obicetrapib in patients at high cardiovascular risk.
Authors: Nicholls S.J.;Nelson A.J.;Ditmarsch M.;Kastelein J.J.P.;Ballantyne C.M.;Ray K.K.;Navar A.M.;Nissen S.E.;Harada-Shiba M.;Curcio D.L.;Neild A.;Kling D.;Hsieh A.;Butters J.;Ference B.A.;Laufs U.;Banach M.;Mehran R.;Catapano A.L.;Huo Y.;Szarek M.;Balinskaite V.;Davidson M.H.
Monash Health Department(s): Cardiology (MonashHeart)
Institution: (Nicholls, Nelson, Butters) Victorian Heart Institute, Monash University, Clayton, VIC, Australia
(Ditmarsch, Kastelein, Curcio, Neild, Kling, Hsieh, Davidson) AmsterdamUnited States
(Kastelein) Department of Vascular Medicine, University of Amsterdam, Amsterdam, United States
(Ballantyne) Baylor College of Medicine, Houston, United States
(Ballantyne) Texas Heart Institute, Houston, United States
(Ray) Imperial College London, London, United Kingdom
(Navar) UT Southwestern Medical Center, Dallas, United States
(Nissen) Cleveland Clinic, Cleveland, United States
(Harada-Shiba) Cardiovascular Center, Osaka Medical and Pharmaceutical University, Osaka, Japan
(Ference) Centre for Naturally Randomized Trials, University of Cambridge, Cambridge, United Kingdom
(Laufs) Klinik und Poliklinik fur Kardiologie, Leipzig University, Leipzig, Germany
(Banach) Department of Preventive Cardiology and Lipidology, Medical University of Lodz, Lodz, Poland
(Mehran, Szarek) Mount Sinai Fuster Heart Hospital, Icahn School of Medicine, Mount Sinai, NY, United States
(Catapano) University of Milan, Milan, United States
(Huo) Peking University First Hospital, Beijing, China
(Szarek) University of Colorado Anschutz Medical Campus, Aurora, United States
(Szarek) State University of New York Downstate School of Public Health, NY, United States
(Balinskaite) MedPace, Cincinnati, United States
Issue Date: 16-May-2025
Copyright year: 2025
Place of publication: United States
Publication information: The New England Journal of Medicine. (no pagination), 2025. Date of Publication: 07 May 2025.
Journal: New England Journal of Medicine
Abstract: BACKGROUND: Obicetrapib is a highly selective cholesteryl ester transfer protein inhibitor that reduces low-density lipoprotein (LDL) cholesterol levels. The efficacy and safety of obicetrapib have not been fully characterized among patients at high risk for cardiovascular events. METHOD(S): We conducted a multinational, randomized, placebo-controlled trial involving patients with heterozygous familial hypercholesterolemia or a history of atherosclerotic cardiovascular disease who were receiving maximum tolerated doses of lipid-lowering therapy. Patients with an LDL cholesterol level of 100 mg per deciliter or higher or a non-high-density lipoprotein (HDL) cholesterol level of 130 mg per deciliter or higher, as well as those with an LDL cholesterol level of 55 to 100 mg per deciliter or a non-HDL cholesterol level of 85 to 130 mg per deciliter and at least one additional cardiovascular risk factor, were eligible for inclusion. The patients were randomly assigned in a 2:1 ratio to receive either 10 mg of obicetrapib once daily or matching placebo for 365 days. The primary end point was the percent change in the LDL cholesterol level from baseline to day 84. RESULT(S): A total of 2530 patients underwent randomization; 1686 patients were assigned to receive obicetrapib and 844 to receive placebo. The mean age of the patients was 65 years, 34% were women, and the mean baseline LDL cholesterol level was 98 mg per deciliter. The least-squares mean percent change from baseline to day 84 in the LDL cholesterol level was -29.9% (95% confidence interval [CI], -32.1 to -27.8) in the obicetrapib group, as compared with 2.7% (95% CI, -0.4 to 5.8) in the placebo group, for a between-group difference of -32.6 percentage points (95% CI, -35.8 to -29.5; P<0.001). The incidence of adverse events appeared to be similar in the two groups. CONCLUSION(S): Among patients with atherosclerotic cardiovascular disease or heterozygous familial hypercholesterolemia who were receiving maximum tolerated doses of lipid-lowering therapy and were at high risk for cardiovascular events, obicetrapib reduced LDL cholesterol levels by 29.9%. (Funded by NewAmsterdam Pharma; BROADWAY ClinicalTrials.gov number, NCT05142722.).Copyright © 2025 Massachusetts Medical Society.
DOI: http://monash.idm.oclc.org/login?url=http://acs.hcn.com.au/?acc=36265&url=https://dx.doi.org/10.1056/NEJMoa2415820
PubMed URL: 40337982
URI: https://repository.monashhealth.org/monashhealthjspui/handle/1/53810
Type: Article In Press
Subjects: cardiovascular disease
cardiovascular risk
coronary atherosclerosis
Type of Clinical Study or Trial: Randomised controlled trial
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