Tucaresol: A Unique Oral Candidate Drug Ideally Accessible for Treatment Of COVID-19 Disease

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Abstract

The SARS-CoV-2 pandemic has significantly impacted world health and economic status. In response, much work has been undertaken to provide effective, safe vaccines, antibodies and antiviral drugs with which to address this pandemic. Treatment of a pandemic population presents multiple challenges in addition to the primary issue of drug efficacy and safety, such as large-scale drug manufacture and distribution, drug stability, oral dosing and pharmacoeconomic considerations. Ideally, these factors must be addressed if new candidate drugs are to be advanced for treatment of large (pandemic) populations. Subsequently, new antivirals have reached the market but choices are few. According to the NIH Covid Treatment Guidelines, only three small molecule antiviral drugs are available to treat COVID-19 disease. As such, a significant part of the research towards discovery of new antiviral drugs has focused on screening and evaluation of ‘repurposed drugs’ or previously approved or clinical stage drugs. Yet, in spite of this increased research activity, one promising clinical stage candidate drug has received little attention regarding its potential as a monotherapy or component of combination therapy for treatment of COVID-19 disease. Tucaresol, with documented human safety and pharmacokinetic data, is an orally active, stable, small molecule amenable to large scale manufacture by a proprietary two-step synthesis developed by us. Tucaresol functions as a host- targeted antiviral by selective protection/reconstitution of CD4+ T helper cells as demonstrated in HIV patients and SIV macaques. In view of similarities between HIV and SARSCoV-2, especially with respect to host CD4+ T helper cells, and the suitability of Tucaresol for facile treatment of pandemic populations, Tucaresol is presented herein for treatment of mild-to- moderate COVID-19 patients but may also be useful for treatment of advanced disease accompanied by lymphopenia.
图卡舒:一种独特的口服候选药物,理想地用于治疗COVID-19疾病
SARS-CoV-2大流行严重影响了世界卫生和经济状况。为此,开展了大量工作,提供有效、安全的疫苗、抗体和抗病毒药物,以应对这一流行病。除了药物有效性和安全性这一主要问题外,治疗大流行人群还面临多重挑战,如大规模药物生产和分销、药物稳定性、口服给药和药物经济学考虑等。理想情况下,如果要推进新的候选药物用于治疗大规模(大流行)人群,就必须解决这些因素。随后,新的抗病毒药物进入市场,但选择很少。根据美国国立卫生研究院Covid -19治疗指南,只有三种小分子抗病毒药物可用于治疗Covid -19疾病。因此,发现新的抗病毒药物的研究的很大一部分集中在筛选和评估“重新用途药物”或先前批准的或临床阶段药物。然而,尽管研究活动有所增加,但一种有前景的临床阶段候选药物作为治疗COVID-19疾病的单一疗法或联合疗法组成部分的潜力却很少受到关注。Tucaresol具有人体安全性和药代动力学数据,是一种口服活性,稳定的小分子,可通过我们开发的专有两步合成方法大规模生产。在HIV患者和SIV猕猴中证实,Tucaresol通过选择性保护/重建CD4+ T辅助细胞作为宿主靶向抗病毒药物。鉴于HIV和SARSCoV-2之间的相似性,特别是在宿主CD4+ T辅助细胞方面,以及Tucaresol对大流行人群的简易治疗的适用性,本文提出Tucaresol用于治疗轻至中度COVID-19患者,但也可用于治疗伴有淋巴细胞减少的晚期疾病。
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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