Literature DB >> 28343601

Effects of RG7652, a Monoclonal Antibody Against PCSK9, on LDL-C, LDL-C Subfractions, and Inflammatory Biomarkers in Patients at High Risk of or With Established Coronary Heart Disease (from the Phase 2 EQUATOR Study).

Amos Baruch1, Sofia Mosesova2, John D Davis2, Nageshwar Budha2, Alexandr Vilimovskij3, Robert Kahn2, Kun Peng2, Kyra J Cowan2, Laura Pascasio Harris2, Thomas Gelzleichter2, Josh Lehrer2, John C Davis2, Whittemore G Tingley4.   

Abstract

RG7652 (MPSK3169A), a fully human immunoglobulin G1 (IgG1) monoclonal antibody directed against proprotein convertase subtilisin/kexin type 9 (PCSK9), blocks the interaction between PCSK9 and low-density lipoprotein (LDL) receptor. EQUATOR (ClinicalTrials.govNCT01609140), a randomized, double-blind, and dose-ranging phase 2 study, evaluated RG7652 in patients (1) at high risk for or (2) with coronary heart disease (CHD). The primary end point was change in LDL cholesterol (LDL-C) from baseline to day 169. Patients (n = 248; median age, 64 years; 57% men; 52% with established CHD; 82% on statins) with baseline LDL-C levels of 90 to 250 mg/dl (mean, 126 mg/dl) continuing on standard-of-care therapy were randomized to receive 1 of 5 RG7652 doses or placebo, subcutaneously every 4, 8, or 12 weeks for 24 weeks. Significant dose-dependent reductions in LDL-C levels from baseline to nadir (56 to 74 mg/dl [48% to 60%]) were observed in all RG7652-dosed patients; effects persisted to day 169 with the highest doses (reduction vs placebo up to 62 mg/dl [51%]) with no unexpected safety signals. RG7652 reduced apolipoprotein B and lipoprotein(a) levels. LDL-C subfraction analysis by nuclear magnetic resonance spectroscopy revealed a prominent decrease in large LDL-C and some decrease in small LDL particles. There was significant reduction in mean particle size of LDL-C on day 169 but no significant reductions in systemic markers of inflammation (high-sensitivity C-reactive protein, interleukin-6, and tumor necrosis factor-alpha). RG7652 reduced LDL-C levels and was well tolerated in patients at high risk for or with CHD on standard-of-care therapy. In conclusion, RG7562 treatment affected large LDL-C and, to a lesser extent, small LDL-C particles; RG7562 did not affect systemic circulating pro-inflammatory cytokines or high-sensitivity C-reactive protein.
Copyright © 2017 Elsevier Inc. All rights reserved.

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Year:  2017        PMID: 28343601     DOI: 10.1016/j.amjcard.2017.02.020

Source DB:  PubMed          Journal:  Am J Cardiol        ISSN: 0002-9149            Impact factor:   2.778


  14 in total

Review 1.  Pleiotropic Anti-atherosclerotic Effects of PCSK9 InhibitorsFrom Molecular Biology to Clinical Translation.

Authors:  Angelos D Karagiannis; Martin Liu; Peter P Toth; Shijia Zhao; Devendra K Agrawal; Peter Libby; Yiannis S Chatzizisis
Journal:  Curr Atheroscler Rep       Date:  2018-03-10       Impact factor: 5.113

2.  Incremental net benefit of lipid-lowering therapy with PCSK9 inhibitors: a systematic review and meta-analysis of cost-utility studies.

Authors:  Bhavani Shankara Bagepally; Akhil Sasidharan
Journal:  Eur J Clin Pharmacol       Date:  2021-10-27       Impact factor: 2.953

Review 3.  PCSK9 Inhibitor Wars: How Does Inclisiran Fit in with Current Monoclonal Antibody Inhibitor Therapy? Considerations for Patient Selection.

Authors:  Natalie Arnold; Wolfgang Koenig
Journal:  Curr Cardiol Rep       Date:  2022-09-10       Impact factor: 3.955

4.  The Influence of Treatment with PCSK9 Inhibitors and Variants in the CRP (rs1800947), TNFA (rs1800629), and IL6 (rs1800795) Genes on the Corresponding Inflammatory Markers in Patients with Very High Lipoprotein(a) Levels.

Authors:  Tina Levstek; Nik Podkrajšek; Andreja Rehberger Likozar; Miran Šebeštjen; Katarina Trebušak Podkrajšek
Journal:  J Cardiovasc Dev Dis       Date:  2022-04-22

5.  Proprotein Convertase Subtilisin/Kexin 9 Levels in Relation to Systemic Immune Activation and Subclinical Coronary Plaque in HIV.

Authors:  Markella V Zanni; Lauren A Stone; Mabel Toribio; Dodie E Rimmelin; Jake Robinson; Tricia H Burdo; Kenneth Williams; Kathleen V Fitch; Janet Lo; Steven K Grinspoon
Journal:  Open Forum Infect Dis       Date:  2017-10-14       Impact factor: 3.835

6.  Susceptibility of low-density lipoprotein particles to aggregate depends on particle lipidome, is modifiable, and associates with future cardiovascular deaths.

Authors:  Maija Ruuth; Su Duy Nguyen; Terhi Vihervaara; Mika Hilvo; Teemu D Laajala; Pradeep Kumar Kondadi; Anton Gisterå; Hanna Lähteenmäki; Tiia Kittilä; Jenni Huusko; Matti Uusitupa; Ursula Schwab; Markku J Savolainen; Juha Sinisalo; Marja-Liisa Lokki; Markku S Nieminen; Antti Jula; Markus Perola; Seppo Ylä-Herttula; Lawrence Rudel; Anssi Öörni; Marc Baumann; Amos Baruch; Reijo Laaksonen; Daniel F J Ketelhuth; Tero Aittokallio; Matti Jauhiainen; Reijo Käkelä; Jan Borén; Kevin Jon Williams; Petri T Kovanen; Katariina Öörni
Journal:  Eur Heart J       Date:  2018-07-14       Impact factor: 29.983

7.  Association of Serum PCSK9 Levels with Antibiotic Resistance and Severity of Disease in Patients with Bacterial Infections Admitted to Intensive Care Units.

Authors:  Tannaz Jamialahmadi; Yunes Panahi; Mohamamd Amin Safarpour; Shiva Ganjali; Mahdi Chahabi; Zeljko Reiner; Saeed Solgi; Amir Vahedian-Azimi; Parisa Kianpour; Maciej Banach; Amirhossein Sahebkar
Journal:  J Clin Med       Date:  2019-10-20       Impact factor: 4.241

8.  Impact of PCSK9 monoclonal antibodies on circulating hs-CRP levels: a systematic review and meta-analysis of randomised controlled trials.

Authors:  Ye-Xuan Cao; Sha Li; Hui-Hui Liu; Jian-Jun Li
Journal:  BMJ Open       Date:  2018-10-04       Impact factor: 2.692

Review 9.  CVD Risk Stratification in the PCSK9 Era: Is There a Role for LDL Subfractions?

Authors:  Christian Abendstein Kjellmo; Anders Hovland; Knut Tore Lappegård
Journal:  Diseases       Date:  2018-05-27

10.  Main differences between two highly effective lipid-lowering therapies in subclasses of lipoproteins in patients with acute myocardial infarction.

Authors:  Leticia C S Pinto; Ana P Q Mello; Maria C O Izar; Nagila R T Damasceno; Antonio M F Neto; Carolina N França; Adriano Caixeta; Henrique T Bianco; Rui M S Póvoa; Flavio T Moreira; Amanda S F Bacchin; Francisco A Fonseca
Journal:  Lipids Health Dis       Date:  2021-09-29       Impact factor: 3.876

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