A Double-blind Multicenter Two-arm Randomized Placebo-controlled Phase-III Clinical Study to Evaluate the Effectiveness and Safety of Thymosin α1 as an Add-on Treatment to Existing Standard of Care Treatment in Moderate-to-severe COVID-19 Patients.

IF 1.5
Adarsh Shetty, Nirhali Sonali Chandrakant, Rahul Ashok Darnule, B G Manjunath, Prachee Sathe
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引用次数: 12

Abstract

Background: From an epidemic outbreak, coronavirus disease-2019 (COVID-19) has quickly developed. Thymosin α1 (Tα1) has the ability to boost the T-cell numbers, support T-cell differentiation, maturation, and reduce cell apoptosis. In this study, we have investigated the efficacy and safety of Tα1 in moderate-to-severe COVID-19 patients.

Patients and methods: In this double-blind, multicenter, two-arm, randomized, placebo-controlled, phase III clinical study, patients were randomized to receive either Tα1 or placebo in combination with standard of care (SOC). The data on all-cause mortality, clinical progression/deterioration, duration of hospital/intensive care unit (ICU) stay, and safety data were collected. The patients were telephonically followed up on Day 28.

Results: A total of (n = 105) COVID-19 patients were included in the study, of which 40 and 65 were severe and moderate, respectively. Thymosin arm (11.1%) had a statistically lower death rate in comparison to the placebo arm (38.5%). A total of 67 adverse events were reported in 42 patients among 105 dosed patients during the study. Among them, 43 adverse events were of mild in nature, 16 adverse events were of moderate in nature, and 8 serious adverse events (death) occurred during the study.

Conclusion: This study provides evidence that Tα1 can lower death rate in severe COVID-19 patients, reduce the load on hospitals by shortening the required number of days of hospitalization and help in abbreviating the requirement of oxygen support by positively impacting the recovery rate and time taken for recovery.

How to cite this article: Shetty A, Chandrakant NS, Darnule RA, Manjunath BG, Sathe P. A Double-blind Multicenter Two-arm Randomized Placebo-controlled Phase-III Clinical Study to Evaluate the Effectiveness and Safety of Thymosin α1 as an Add-on Treatment to Existing Standard of Care Treatment in Moderate-to-severe COVID-19 Patients. Indian J Crit Care Med 2022;26(8):913-919.

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一项双盲、多中心、两组随机、安慰剂对照的iii期临床研究,评估胸腺素α1作为现有标准护理治疗的补充治疗在中重度COVID-19患者中的有效性和安全性。
背景:2019冠状病毒病(COVID-19)自疫情暴发以来迅速发展。胸腺素α1 (t - α1)具有增加t细胞数量、支持t细胞分化、成熟和减少细胞凋亡的作用。在这项研究中,我们研究了t - α1在中重度COVID-19患者中的疗效和安全性。患者和方法:在这项双盲、多中心、两组、随机、安慰剂对照的III期临床研究中,患者随机接受t - α1或安慰剂联合标准治疗(SOC)。收集了全因死亡率、临床进展/恶化、住院/重症监护病房(ICU)住院时间和安全性数据。第28天对患者进行电话随访。结果:共纳入(n = 105)例COVID-19患者,其中重度40例,中度65例。胸腺素组(11.1%)的死亡率低于安慰剂组(38.5%)。在105名给药患者中,42名患者共报告了67例不良事件。其中,轻度不良事件43例,中度不良事件16例,研究期间发生严重不良事件(死亡)8例。结论:本研究证明Tα1可降低COVID-19重症患者的死亡率,通过缩短住院天数减轻医院负担,并通过积极影响恢复率和恢复时间缩短氧支持需求。Shetty A, Chandrakant NS, Darnule RA, Manjunath BG, Sathe P. A双盲多中心随机安慰剂对照iii期临床研究:胸腺素α1作为现有标准护理治疗的补充治疗的有效性和安全性。中华检验医学杂志(英文版);2009;26(8):913-919。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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