Obicetrapib on Top of Maximally Tolerated Lipid-Modifying Therapies in Participants With or at High Risk for Atherosclerotic Cardiovascular Disease: Rationale and Designs of BROADWAY and BROOKLYN.

apolipoprotein B atherosclerotic cardiovascular disease cholesteryl ester transfer protein heterozygous familial hypercholesterolemia lipoprotein(a) low-density lipoprotein cholesterol obicetrapib

Journal

American heart journal
ISSN: 1097-6744
Titre abrégé: Am Heart J
Pays: United States
ID NLM: 0370465

Informations de publication

Date de publication:
03 May 2024
Historique:
received: 14 03 2024
revised: 01 05 2024
accepted: 01 05 2024
medline: 6 5 2024
pubmed: 6 5 2024
entrez: 5 5 2024
Statut: aheadofprint

Résumé

Obicetrapib, a novel, selective cholesteryl ester transfer protein (CETP) inhibitor, reduces low-density lipoprotein cholesterol (LDL-C), LDL particles, apolipoprotein (Apo) B, and lipoprotein(a) [Lp(a)] and increases high-density lipoprotein cholesterol (HDL-C) when added to statins with or without ezetimibe. By substantially reducing LDL-C, obicetrapib has the potential to lower atherogenic lipoproteins in patients with atherosclerotic cardiovascular disease (ASCVD) or heterozygous familial hypercholesterolemia (HeFH) whose LDL-C levels remain high despite treatment with available maximally tolerated lipid-modifying therapies, addressing an unmet medical need in a patient population at high risk for cardiovascular events. BROADWAY (NCT05142722) and BROOKLYN (NCT05425745) are ongoing placebo-controlled, double-blind, randomized Phase III trials designed to examine the efficacy, safety, and tolerability of obicetrapib as an adjunct to dietary intervention and maximally tolerated lipid-modifying therapies in participants with a history of ASCVD and/or underlying HeFH whose LDL-C is not adequately controlled. The primary efficacy endpoint was the percent change in LDL-C from baseline to day 84. Other endpoints included changes in Apo B, non-HDL-C, HDL-C, Apo A1, Lp(a) and triglycerides in addition to parameters evaluating safety, tolerability, and pharmacokinetics. BROADWAY also included an adjudicated assessment of major adverse cardiovascular events, measurements of glucose homeostasis, and an ambulatory blood pressure monitoring substudy. A total of 2532 participants were randomized in BROADWAY and 354 in BROOKLYN to receive obicetrapib 10 mg or placebo (2:1) for 365 days with follow-up through 35 days after the last dose. Results from both trials are anticipated in 2024. These trials will provide safety and efficacy data to support the potential use of obicetrapib among patients with ASCVD or HeFH with elevated LDL-C for whom existing therapies are not sufficiently effective or well-tolerated.

Identifiants

pubmed: 38705341
pii: S0002-8703(24)00116-9
doi: 10.1016/j.ahj.2024.05.002
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024. Published by Elsevier Inc.

Déclaration de conflit d'intérêts

Declaration of competing interest Stephen J. Nicholls received grant/research support from AstraZeneca, New Amsterdam Pharma, Amgen, Anthera, Eli Lilly, Esperion, Novartis, Cerenis, The Medicines Company, Resverlogix, InfraReDx, Roche, Sanofi-Regeneron, and LipoScience; and was a consultant for AstraZeneca, Amarin, Akcea, Eli Lilly, Anthera, Omthera, Merck, Takeda, Resverlogix, Sanofi-Regeneron, CSL Behring, Esperion, Boehringer Ingelheim, and Vaxxinity. Adam J. Nelson received personal fees from Boehringer Ingelheim, AstraZeneca, Amgen, Novartis, and Sanofi. Marc Ditmarsch is Chief Development Officer for NewAmsterdam Pharma. John J.P. Kastelein is Chief Scientific Officer for NewAmsterdam Pharma and Emeritus Professor of Medicine at the University of Amsterdam, The Netherlands. Christie M. Ballantyne received grant/research support (all paid to the institution, not individual) from Abbott Diagnostic, Akcea, Amgen, Arrowhead, Esperion, Ionis, Merck, NewAmsterdam Pharma, Novartis, Novo Nordisk, Regeneron, Roche Diagnostic, NIH, AHA, and ADA and was a consultant for 89Bio, Abbott Diagnostics, Alnylam Pharmaceuticals, Althera, Amarin, Amgen, Arrowhead, AstraZeneca, Denka Seiken, Esperion, Genentech, Gilead, Illumina, Ionia, Lilly, Matinas BioPharma Inc., Merck, NewAmsterdam Pharma, Novartis, Novo Nordisk, Pfizer, Regeneron, and Roche Diagnostic. Kausik K. Ray reports his institution received unrestricted research grants from Amgen, Daiichi Sankyo, Regeneron, and Sanofi; consulting or advisory board honoraria from Novartis, Esperion, Daiichi Sankyo, Abbott, Bayer, Eli Lilly, Silence Therapeutics, CSL Behring, NewAmsterdam Pharma, Sanofi, Amgen Novo Nordisk, BI, Scribe, Vaxxinity, CRISPR, AZ, Kowa, and Cargene; honoraria for CME and non-CME from Novartis, Novo Nordisk, BI, AZ, Viatris, Daiichi Sankyo, Amgen, and Sanofi; and he has stock options from PEMI-31. Ann Marie Navar reports honoraria and consulting fees from AstraZeneca, Bayer, Bristol Meyer Squibb, Boehringer Ingelheim, Esperion, Janssen, Eli Lilly, Merck, NewAmsterdam Pharma, Novartis, NovoNordisk, Pfizer, and Silence Therapeutics; and funding for research to her institution from Esperion, Janssen, and Amgen. Steven E. Nissen reports that Cleveland Clinic Center for Clinical Research has received funding to perform clinical trials from Abbvie, AstraZeneca, Amgen, Arrowhead, Bristol Myers Squibb, Eli Lilly, Esperion, Medtronic, MyoKardia, NewAmsterdam Pharma, Novartis, Pfizer, and Silence Therapeutics. Dr. Nissen is involved in these clinical trials but receives no personal renumeration for his participation and consults for these pharmaceutical companies but does not accept compensation. Anne C. Goldberg has received research grant(s)/support from Amarin, Amgen, Akcea/IONIS, Arrowhead, Esperion Therapeutics, Inc., Merck, NewAmsterdam Pharma, Novartis, Pfizer, Regeneron, and Sanofi; has served as a consultant for 23andMe, Akcea, Esperion, IONIS, Merck, NewAmsterdam Pharma, Novartis, OptumRX, Regeneron, and Sanofi; and has provided editorial work for Merck. Liam R. Brunham is Reserch Chair, Associate Professor for The University of British Columbia. Danielle Curcio is Executive Director of Clinical Operations for NewAmsterdam Pharma. Erin Wuerdeman is Executive Director of Clinical Operations for NewAmsterdam Pharma. Annie Nield is Executive Vice President and Head of Global Regulatory Affairs for NewAmsterdam Pharma. Douglas Kling is Chief Operating Officer for NewAmsterdam Pharma. Andrew Hsieh is Vice President of Medical Affairs for NewAmsterdam Pharma. Mary R. Dicklin is an employee of Midwest Biomedical Research, which has received consulting fees and/or grant funding from NewAmsterdam Pharma, Acasti Pharma, Beren Therapeutics, Eli Lilly and Company, Indiana University and Foundation, Matinas BioPharma, NorthSea Therapeutics, and 89Bio. Brain A. Ference reports research grants from Merck, Novartis, Amgen, and Esperion Therapeutics, and consulting fees, advisory boards, or lecture honoraria from Novartis, Merck, Amgen, Regeneron, Sanofi, Novartis, Pfizer, Eli Lilly, Novo Nordisk, Daiichi-Sankyo, Viatris, Ionis Pharmaceuticals, NewAmsterdam Pharma, dalCOR, The Medicines Co., Mylan, CiVi Pharma, KrKa Pharmaceuticals, American College of Cardiology, EAS, and European Society of Cardiology. Ulrich Laufs has received honoraria from Amgen, Daiichi Sankyo, MSD, Novartis, and Sanofi. Maciej Banach has received renumeration for lectures from Adamed, Amgen, Daiichi Sankyo, Exceed Orphan, KRKA Polypharma, Mylan/Viatris, Novartis, Novo Nordisk, Pfizer, Sanofi, Teva, and Zentiva; participated in advisory panels for Adamed, Amgen, Daiichi Sankyo, Esperion, NewAmsterdam Pharma, Novartis, Novo Nordisk, and Sanofi; and received grants from Amgen, Daiichi Sankyo, Mylan/Viatris, and Sanofi. Roxana Mehran has institutional research grants from Abbott, Abiomed, Alleviant Medical, Amgen, AM-Pharma, Applied Therapeutics, Arena Pharmaceuticals, AstraZeneca, Biosensors, Biotronik, Boston Scientific, Bristol Myers Squibb, Cardiawav, CeloNova, Chiesi, Concept Medical, CSL Behring, CytoSorbents, Daiichi Sankyo, Element Science, Faraday Pharmaceuticals, Humacyte, Idorsia Pharmaceuticals, I-Laser, Janssen, Magenta Medical, Mediasphere Medical, Medtelligence, Medtronic, Novartis, OrbusNeich, Penumbra, PhaseBio, Philips, Pi-Cardia, PLx Pharma, Protembis, RenalPro, RM Global, Shockwave, Transverse Medical, Vivasure, and ZOLL Medical; consulting fees from AstraZeneca, Novartis, Cine-Med Research, Ionis Pharmaceuticals, Novo Nordisk, Vectura Inc., and WebMD; honoraria from Novartis Pharmaceuticals, Philips Electronics, Biotronik Inc., and Bayer Healthcare Pharmaceuticals; advisory board participation for Humacyte Inc., PhaseBio, Faraday Pharmaceuticals, Medtronic, Philips, and PLx Pharma; participation on a data safety monitoring board for Pi-Cardia; a leadership role with the American Medical Association (JAMA Cardiology, associate editor), American College of Cardiology (BOT Member, SC Member CTR Program), and Society for Cardiovascular Angiography & Interventions (Women in Innovations Committee Member); stock or stock options from Applied Therapeutics, Elixir Medical, Stel, and ControlRad; and faculty membership with the Cardiovascular Research Foundation. Alberico L. Catapano in the last three years has received honoraria, lecture fees, or research grants from Aegerion, Amarin, Amgen, Amryt Pharma, AstraZeneca, Daiichi Sankyo, Esperion, Ionis Pharmaceutical, Medscape Education, Menarini, MSD, NewAmsterdam Pharma, Novartis, NovoNordisk, PeerVoice, Pfizer, Recordati, Regeneron, Sanofi, The Corpus, Ultragenyx, and Viatris. Michael H. Davidson is Chief Executive Officer for NewAmsterdam Pharma.

Auteurs

Stephen J Nicholls (SJ)

Victorian Heart Institute, Monash University, Victoria, Australia. Electronic address: stephen.nicholls@monash.edu.

Adam J Nelson (AJ)

Victorian Heart Institute, Monash University, Victoria, Australia.

Marc Ditmarsch (M)

NewAmsterdam Pharma, Naarden, The Netherlands.

John J P Kastelein (JJP)

NewAmsterdam Pharma, Naarden, The Netherlands.

Christie M Ballantyne (CM)

Baylor College of Medicine and the Texas Heart Institute, Houston, TX, USA.

Kausik K Ray (KK)

Department of Primary Care and Public Health, Imperial College London, London, UK.

Ann Marie Navar (AM)

University of Texas Southwestern Medical Center, Dallas, TX, USA.

Steven E Nissen (SE)

Cleveland Clinic Lerner School of Medicine at Case Western Reserve University, Cleveland, OH, USA.

Anne C Golberg (AC)

Washington University School of Medicine, St. Louis, MO, USA.

Liam R Brunham (LR)

UBC Centre for Heart Lung Innovation, The University of British Columbia, Vancouver, British Columbia, Canada.

Danielle Curcio (D)

NewAmsterdam Pharma, Naarden, The Netherlands.

Erin Wuerdeman (E)

NewAmsterdam Pharma, Naarden, The Netherlands.

Annie Neild (A)

NewAmsterdam Pharma, Naarden, The Netherlands.

Douglas Kling (D)

NewAmsterdam Pharma, Naarden, The Netherlands.

Andrew Hsieh (A)

NewAmsterdam Pharma, Naarden, The Netherlands.

Mary R Dicklin (MR)

Midwest Biomedical Research, Addison, IL, USA.

Brian A Ference (BA)

Centre for Naturally Randomized Trials, University of Cambridge, Cambridge, UK.

Ulrich Laufs (U)

Klinik und Poliklinkk für Kardiologie, Leipzig University, Germany.

Maciej Banach (M)

Department of Preventive Cardiology and Lipidologym, Medical University of Lodz (MUL), Lodz, Poland.

Roxana Mehran (R)

The Zena and Michael A. Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Alberico L Catapano (AL)

IRCCS MultiMedica, Milan, Italy; Department of Pharmacological and Biomolecular Sciences, University of Milan, Milan, Italy.

Michael H Davidson (MH)

NewAmsterdam Pharma, Naarden, The Netherlands.

Classifications MeSH