Codivir抑制SARS-Cov-2病毒复制并稳定临床结果:体外和I期临床试验结果

Yotam Kolben, Eynat Finkelshtein, Esmira Naftali, Ariel Kenig, Asa Kessler, Florentino Cardoso, Nadya Lisovoder, Asaf Schwartz, Daniel Elbirt, Shlomo Maayan, Yaron Ilan
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摘要

背景:面对全球发病率和死亡率不断上升的情况,严重急性呼吸窘迫综合征冠状病毒2 (SARS-CoV-2)的治疗仍然是一项重大挑战。SARS-CoV-2引起的急性疾病由病毒阶段开始,随后是炎症阶段。许多抗炎和抗病毒治疗,临床效果相对较小,已被应用。开发一种安全有效的直接抗病毒治疗方法至关重要,因为它可以在出现严重并发症之前阻止疾病进展,并有可能预防传播。目的:本研究旨在确定新开发的抗病毒药物Codivir的安全性,并初步评估其对COVID-19感染患者的抗病毒活性。方法:采用免疫荧光法测定Codivir的直接抗病毒作用,并采用四氮唑法(MTT)评价其细胞毒作用。在一期临床试验中,12名患者服用Codivir 10天,以确保其安全性。随访患者给药期间的临床表现。在治疗前和治疗期间测定顺序鼻病毒PCR滴度(周期阈值,CT)。结果:Codivir在体外对SARS-CoV-2具有抑制90%病毒复制和最小细胞毒性的活性。抗病毒活性在病毒进入细胞后感染的早期阶段被证实。Codivir在所有12例I期临床试验患者中是安全的,在5/7的完全评估患者中显著抑制病毒复制,抗病毒效果早在3天就被发现。总结:本研究的数据支持Codivir在人体内的安全性,并提示其具有显著的抗covid -19作用。这些结果支持在SARS-CoV-2患者中进行更广泛的对照试验来测试该药物。
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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Codivir suppresses SARS-Cov-2 viral replication and stabilizes clinical outcome: In vitro and Phase I clinical trial results.

Background: Treatment of severe acute respiratory distress syndrome coronavirus 2 (SARS-CoV-2) remains a significant challenge in the face of increased worldwide morbidity and mortality. The acute illness caused by SARS-CoV-2 is initiated by a viral phase, followed by an inflammatory phase. Numerous anti-inflammatory and anti-viral therapies, with a relatively minor clinical effect, have been applied. Developing a safe and efficient direct anti-viral treatment is essential as it can block disease progression before significant complications ensue and potentially prevent transmission.

Aim: The present phase 1 study aimed to determine the safety of Codivir, a newly developed anti-viral agent, and to preliminarily assess its anti-viral activity in patients infected by COVID-19.

Methods: In vitro studies were conducted to determine the direct anti-viral effect of Codivir using an immunofluorescence-based assay and to assess its cytotoxic effect by tetrazolium assay (MTT). In a phase I clinical trial, Codivir was administered for ten days in 12 patients who were followed for its safety. Patients were followed for clinical manifestations during administration. Sequential nasal viral PCR titers (Cycle Threshold, CT) were determined preceding and during treatment.

Results: In vitro, Codivir showed activity against SARS-CoV-2 with 90% viral replication suppression and minimal cytotoxicity. The anti-viral activity was demonstrated at the early stages of infection, post-entry of the virus in the cell. Codivir was safe in all 12 patients in phase I clinical trial and significantly suppressed viral replication in 5/7 fully assessed patients, with an anti-viral effect noted as early as three days.

Summary: The present study's data support the safety of Codivir administration in humans and suggest its significant anti-COVID-19 effect. These results support the testing of the drug in more extensive controlled trials in patients with SARS-CoV-2.

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