RNA Polymerase Inhibitor Enisamium for Treatment of Moderate COVID-19 Patients: A Randomized, Placebo-Controlled, Multicenter, Double-Blind Phase 3 Clinical Trial.

IF 1.8 Q3 RESPIRATORY SYSTEM Advances in respiratory medicine Pub Date : 2024-05-06 DOI:10.3390/arm92030021
Olga Holubovska, Pavlo Babich, Alla Mironenko, Jens Milde, Yuriy Lebed, Holger Stammer, Lutz Mueller, Aartjan J W Te Velthuis, Victor Margitich, Andrew Goy
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Abstract

Enisamium is an orally available therapeutic that inhibits influenza A virus and SARS-CoV-2 replication. We evaluated the clinical efficacy of enisamium treatment combined with standard care in adult, hospitalized patients with moderate COVID-19 requiring external oxygen. Hospitalized patients with laboratory-confirmed SARS-CoV-2 infection were randomly assigned to receive either enisamium (500 mg per dose, four times a day) or a placebo. The primary outcome was an improvement of at least two points on an eight-point severity rating (SR) scale within 29 days of randomization. We initially set out to study the effect of enisamium on patients with a baseline SR of 4 or 5. However, because the study was started early in the COVID-19 pandemic, and COVID-19 had been insufficiently studied at the start of our study, an interim analysis was performed alongside a conditional power analysis in order to ensure patient safety and assess whether the treatment was likely to be beneficial for one or both groups. Following this analysis, a beneficial effect was observed for patients with an SR of 4 only, i.e., patients with moderate COVID-19 requiring supplementary oxygen. The study was continued for these COVID-19 patients. Overall, a total of 592 patients were enrolled and randomized between May 2020 and March 2021. Patients with a baseline SR of 4 were divided into two groups: 142 (49.8%) were assigned to the enisamium group and 143 (50.2%) to the placebo group. An analysis of the population showed that if patients were treated within 4 days of the onset of COVID-19 symptoms (n = 33), the median time to improvement was 8 days for the enisamium group and 13 days for the placebo group (p = 0.005). For patients treated within 10 days of the onset of COVID-19 symptoms (n = 154), the median time to improvement was 10 days for the enisamium group and 12 days for the placebo group (p = 0.002). Our findings suggest that enisamium is safe to use with COVID-19 patients, and that the observed clinical benefit of enisamium is worth reporting and studying in detail.

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治疗中度 COVID-19 患者的 RNA 聚合酶抑制剂 Enisamium:随机、安慰剂对照、多中心、双盲 3 期临床试验。
依尼沙明是一种抑制甲型流感病毒和 SARS-CoV-2 复制的口服治疗药物。我们评估了在需要外部供氧的中度 COVID-19 住院成年患者中将依尼沙明治疗与标准护理相结合的临床疗效。经实验室确诊感染了 SARS-CoV-2 的住院患者被随机分配接受依尼沙明(每次 500 毫克,每天 4 次)或安慰剂治疗。主要结果是在随机分配后的 29 天内,在八分严重程度评分表(SR)上至少改善两分。我们最初打算研究依尼沙明对基线 SR 为 4 或 5 的患者的影响。然而,由于研究是在 COVID-19 大流行初期开始的,而在我们的研究开始时,对 COVID-19 的研究还不够充分,因此我们在进行条件功率分析的同时还进行了中期分析,以确保患者的安全,并评估治疗是否可能对其中一组或两组患者都有益。分析结果显示,只有 SR 值为 4 的患者(即需要补充氧气的中度 COVID-19 患者)能从中获益。对这些 COVID-19 患者的研究继续进行。总体而言,2020 年 5 月至 2021 年 3 月期间,共有 592 名患者入组并进行了随机分组。基线SR为4的患者被分为两组:142人(49.8%)被分配到依尼沙明组,143人(50.2%)被分配到安慰剂组。对人群的分析表明,如果患者在出现 COVID-19 症状 4 天内接受治疗(n = 33),那么恩利沙明组的中位改善时间为 8 天,安慰剂组为 13 天(p = 0.005)。对于在 COVID-19 症状出现后 10 天内接受治疗的患者(n = 154),烯酰胺组的中位改善时间为 10 天,安慰剂组为 12 天(p = 0.002)。我们的研究结果表明,对 COVID-19 患者使用依尼沙明是安全的,而且观察到的依尼沙明临床益处值得详细报告和研究。
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来源期刊
Advances in respiratory medicine
Advances in respiratory medicine RESPIRATORY SYSTEM-
CiteScore
2.60
自引率
0.00%
发文量
90
期刊介绍: "Advances in Respiratory Medicine" is a new international title for "Pneumonologia i Alergologia Polska", edited bimonthly and addressed to respiratory professionals. The Journal contains peer-reviewed original research papers, short communications, case-reports, recommendations of the Polish Respiratory Society concerning the diagnosis and treatment of lung diseases, editorials, postgraduate education articles, letters and book reviews in the field of pneumonology, allergology, oncology, immunology and infectious diseases. "Advances in Respiratory Medicine" is an open access, official journal of Polish Society of Lung Diseases, Polish Society of Allergology and National Research Institute of Tuberculosis and Lung Diseases.
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