Hegazy Sahar K, Tharwat Samar, Hassan Ahmed H
Clinical Pharmacy Department, Faculty of Pharmacy, Tanta University, Tanta, PC: 31511, Egypt.
Rheumatology and Immunology Department, Faculty of Medicine, Mansoura University, Mansoura, PC: 35511, Egypt.
Open Med (Wars). 2023 Aug 9;18(1):20230768. doi: 10.1515/med-2023-0768. eCollection 2023.
Coronavirus disease 2019 (COVID-19) caused a progress in research to find a solution to this pandemic. Also, various advances in pharmacotherapy against COVID-19 have emerged. Regarding antiviral therapy, casirivimab and imdevimab are antibodies combination against COVID-19. Standard antiviral therapy against COVID-19 includes remdesivir and favipiravir. The objectives were to compare progression and multi-organ function of hospitalized COVID-19 patients between these three antiviral groups. 265 COVID-19 hospitalized patients were included in this study and were divided into 3 groups (1:2:2), respectively, Group (A): casirivimab and imdevimab, group (B): remdesivir, and group (C): favipiravir. The design of the study is a single blind non-randomized controlled trial. This study is a phase IV clinical trial (post-marketing study). The duration of the study was about 6 months after receiving the ethical approval. Casirivimab and imdevimab achieved less case progression as presented by lower World Health Organization scale ( < 0.05 in comparing group A with B and C) and better multi-organ functions as presented by lower Sequential Organ Function Assessment score ( < 0.05 in comparing group A with B and C) than remdesivir and favipiravir. From all these results, it is concluded that Group A (casirivimab and imdevimab) produces better outcomes than B (remdesivir) and C (favipiravir) intervention groups.
2019冠状病毒病(COVID-19)推动了针对这一疫情解决方案的研究进展。同时,针对COVID-19的药物治疗也取得了各种进展。在抗病毒治疗方面,卡西瑞维单抗和英迪维单抗是针对COVID-19的抗体组合。针对COVID-19的标准抗病毒治疗包括瑞德西韦和法匹拉韦。目的是比较这三个抗病毒治疗组中住院COVID-19患者的病情进展和多器官功能。本研究纳入了265例住院的COVID-19患者,并将其分为3组(1:2:2),分别为:A组:卡西瑞维单抗和英迪维单抗;B组:瑞德西韦;C组:法匹拉韦。本研究设计为单盲非随机对照试验。本研究为IV期临床试验(上市后研究)。研究持续时间为获得伦理批准后的约6个月。与瑞德西韦和法匹拉韦相比,卡西瑞维单抗和英迪维单抗导致的病例进展更少,这表现为较低的世界卫生组织分级(A组与B组和C组比较,P<0.05),多器官功能更好,这表现为较低的序贯器官功能评估评分(A组与B组和C组比较,P<0.05)。从所有这些结果可以得出结论,A组(卡西瑞维单抗和英迪维单抗)比B组(瑞德西韦)和C组(法匹拉韦)干预组产生更好的结果。