Department of Molecular and Clinical Pharmacology, University of Liverpool, Liverpool, UK.
National Hemophilia Center, Tel Aviv, Israel.
J Antimicrob Chemother. 2020 Sep 1;75(9):2381-2383. doi: 10.1093/jac/dkaa272.
The development of therapeutic agents against SARS-CoV-2/COVID-19 faces numerous barriers and a multidisciplinary approach to evaluating drug efficacy and toxicity is essential. Experimental and preclinical data should be integrated into a comprehensive analysis, where drug potency, the timing of therapy initiation, drug combinations, variability in systemic and local drug exposure and short- and long-term toxicities represent fundamental factors for the rational identification of candidates and prioritization of clinical investigations. Although the identification of SARS-CoV-2 therapeutics is a priority, rigorous and transparent methodologies are crucial to ensure that accelerated research programmes result in high-quality and reproducible findings.
针对 SARS-CoV-2/COVID-19 的治疗药物的开发面临着众多障碍,因此需要采取多学科方法来评估药物的疗效和毒性。应将实验和临床前数据整合到综合分析中,其中药物效力、治疗开始时间、药物组合、全身和局部药物暴露的可变性以及短期和长期毒性是合理鉴定候选药物和优先进行临床研究的基本因素。虽然鉴定 SARS-CoV-2 的治疗方法是当务之急,但严格和透明的方法对于确保加速研究计划产生高质量和可重复的结果至关重要。