Hypercholesterolemia: a literature review on management using tafolecimab: a novel member of PCSK9 monoclonal antibodies

Author:

Qureshi Zaheer1,Khanzada Mikail2,Safi Adnan3,Fatima Eeshal4,Altaf Faryal5,Vittorio Timothy J.6

Affiliation:

1. The Frank H. Netter M.D. School of Medicine at Quinnipiac University, Bridgeport, CT

2. Department of Internal Medicine, Lahore Medical & Dental College

3. Department of Medicine, Lahore General Hospital

4. Department of Medicine, Services Institute of Medical Sciences, Lahore, Pakistan

5. Department of Internal Medicine, Icahn School of Medicine at Mount Sinai/BronxCare Health System

6. Department of Internal Medicine, BronxCare Health System, New York, NY

Abstract

Background: Cardiovascular diseases (CVD) persist as the leading cause of mortality globally, with atherosclerotic cardiovascular disease (ASCVD), including hypercholesterolaemia, being a significant contributor. Hyperlipidemia management includes various lipid-lowering drugs, including statins, Bempedoic acid, inclisiran, Lomitapide, ANGPTL3 inhibitors, and PCSK9 inhibitors. Statins have traditionally dominated lipid management therapies; however, a subset of patients remains unresponsive or intolerant to this therapy, necessitating novel therapeutic approaches. Tafolecimab, a promising and novel PCSK9 monoclonal antibody, demonstrated significant LDL-C reduction and a favourable safety profile in clinical trials. Objective: This review aimed to discuss the role and efficacy of Tafolecimab in the management of hypercholesterolaemia. Methods: The authors searched online databases, including PubMed, Scopus, and Embase, for articles related to talofecimab. Discussion: The efficacy of Tafolecimab in diverse patient populations, including those with comorbid conditions and various lipid disorders, has been explored. Ongoing trials, such as CREDIT-1, CREDIT-2, and CREDIT-4, have provided valuable insights into Tafolecimab’s potential as a lipid-lowering agent. Moreover, the drug’s extended dosing interval may enhance patient compliance and reduce treatment costs. It has also been found that Tafolecimab has more affinity for PCSK9 and a longer duration of LDL-C reduction than other monoclonal antibody drugs such as evolocumab. Thus, this review focuses on Tafolecimab, a novel PCSK9 monoclonal antibody, its mechanism of action, clinical trial outcomes, safety profile, and potential role in hypercholesterolaemia management. Despite its assuring potential, the long-term impact of Tafolecimab on cardiovascular outcomes remains to be fully elucidated, necessitating further research. Regulatory authorities like the FDA and EMA should also evaluate Tafolecimab’s risks and benefits. Conclusion: In conclusion, Tafolecimab shows potential as an innovative therapeutic option for hypercholesterolaemia, particularly in patients with specific risk factors, but warrants additional research.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Reference114 articles.

1. The global burden of cardiovascular diseases and risk: a compass for future health;Vaduganathan;J Am Coll Cardiol,2022

2. 2018 AHA/ACC/AACVPR/AAPA/ABC/ACPM/ADA/AGS/APhA/ASPC/NLA/PCNA guideline on the management of blood cholesterol: a report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines;Grundy;Circulation,2019

3. Low-density lipoprotein cholesterol: lower is totally better;Cannon;J Am Coll Cardiol,2020

4. Efficacy and safety of cholesterol-lowering treatment: prospective meta-analysis of data from 90 056 participants in 14 randomised trials of statins;Lancet,2005

5. Ezetimibe added to statin therapy after acute coronary syndromes;Cannon;New Engl J Med,2015

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