ECONOMIC ASPECTS OF APPLICATION OF THE RUSSIAN BIOSIMILAR OMALIZUMAB IN PATIENTS WITH ATOPIC BRONCHIAL ASTHMA OF MODERATE TO SEVERE CLINICAL COURSES

V. Krysanova, E. D. Ermolaeva, T. Ermolaeva, M. Davydovskaya, K. Kokushkin
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引用次数: 2

Abstract

A certain success in the treatment of bronchial asthma is associated with the introduction of monoclonal antibodies into the treatment process. They made it possible to improve the control of the disease. A number of original genetically engineered biological drugs, such as benralizumab, reslizumab, dupilumab, mepolizumab and omalizumab, are currently registered in Russia. In 2020, this list was supplemented by the first Russian biosimilar drug omalizumab – Genolar® (JSC Generium, Russia). High rates of the development of modern medicine are closely related to the use of biosimilars. The prescription of biosimilars today often makes it possible to provide a larger number of patients with modern drugs at lower costs.The aim of the study was a comprehensive pharmacoeconomic assessment of the application of the domestic biosimilar drug omalizumab in the treatment of patients suffering from moderate and severe atopic bronchial asthma.Materials and methods. At the first stage, an information search in the available databases (Cochrane Library, MedLine, Embase, eLIBRARY) was carried out. According to the results obtained, a meta-analysis (Agache I. et al.) was found out; within its framework, the efficacy and safety of the use of several monoclonal antibodies was assessed. Dupilumab was chosen as the reference drug. Pharmacoeconomic analyses were carried out using a “Cost-Minimization Analysis” (CMA) and a “Budget Impact Analysis” (BIA). Taking into account various options of bronchial asthma, the developed algorithm for providing medical care to adult patients with atopic asthma made it possible to assess the costs, including direct medical and indirect costs.Results. The cost analysis demonstrated the advantage of using the Russian biosimilar omalizumab in patients with atopic asthma compared to dupilumab due to financial savings of up to 40%. The Budget Impact Analysis showed that the use of the domestic biosimilar omalizumab, even taking into account the annual increase in the number of patients (8%), will save up to 109,641,409.64 rubles (or 3%) compared to the current practice.Conclusion. The use of the domestic biosimilar omalizumab in patients with moderate to severe atopic bronchial asthma is a clinically effective and economically justified approach to organizing medical care for adult patients in Russia.
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俄罗斯生物仿制药omalizumab在中度至重度临床病程的特应性支气管哮喘患者中的应用的经济方面
支气管哮喘治疗的一定成功与在治疗过程中引入单克隆抗体有关。他们使改善对疾病的控制成为可能。一些原基因工程生物药物,如benralizumab, reslizumab, dupilumab, mepolizumab和omalizumab,目前在俄罗斯注册。2020年,俄罗斯首个生物仿制药omalizumab - Genolar®(JSC Generium,俄罗斯)补充了该清单。现代医学的高速发展与生物仿制药的使用密切相关。如今,生物仿制药的处方往往能够以较低的成本为更多的患者提供现代药物。本研究的目的是对国产生物仿制药omalizumab在中重度特应性支气管哮喘患者治疗中的应用进行综合药物经济学评价。材料和方法。在第一阶段,在可用的数据库(Cochrane Library, MedLine, Embase, eLIBRARY)中进行信息检索。根据所得结果,进行meta分析(Agache I. et al.);在其框架内,评估了几种单克隆抗体使用的有效性和安全性。选择Dupilumab作为对照药物。使用“成本最小化分析”(CMA)和“预算影响分析”(BIA)进行药物经济学分析。考虑到支气管哮喘的各种选择,所开发的为成人特应性哮喘患者提供医疗护理的算法使评估成本成为可能,包括直接医疗成本和间接成本。成本分析表明,与dupilumab相比,俄罗斯生物仿制药omalizumab在特应性哮喘患者中使用的优势在于节省高达40%的资金。预算影响分析显示,使用国产生物仿制药omalizumab,即使考虑到患者数量每年增加(8%),与目前的做法相比,将节省高达109,641,409.64卢布(或3%)。在俄罗斯,使用国产生物仿制药omalizumab治疗中度至重度特应性支气管哮喘患者是一种临床有效且经济合理的方法,可以为成年患者组织医疗保健。
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