Office of Clinical Pharmacology, Office of Translational Science, Center for Drug Evaluation and Research, 10903 New Hampshire Avenue, Silver Spring, Maryland 20993.
Office of Clinical Pharmacology, Office of Translational Science, Center for Drug Evaluation and Research, 10903 New Hampshire Avenue, Silver Spring, Maryland 20993.
J Pharm Sci. 2019 Feb;108(2):798-806. doi: 10.1016/j.xphs.2018.09.010. Epub 2018 Sep 19.
There are no approved drugs or biologics to treat Ebola virus disease (EVD). Literature reviews identified a list of 141 drugs with reports of preliminary in vitro potency and in vivo effectiveness in animals or with reports of clinical use/trials in EVD patients. The majority of these drugs have been individually approved by the U.S. Food and Drug Administration for treating various non-EVD diseases. The anti-Ebola potency data of these drugs were curated from literature and publicly accessible databases, along with their individual biopharmaceutical and pharmacokinetic characteristics. To facilitate the development of antiviral drugs including anti-EVD drugs, highlights include optimization of the exposure-response relationship, design of a safe and effective clinical dosing regimen to achieve an adequate high ratio of clinical C to a plasma protein binding-adjusted EC, and the pharmacokinetic studies needed in animal models (healthy and affected) and in healthy volunteers. The exposure/response relationship for human dose selection is summarized, as described in the U.S. Food and Drug Administration "Animal Rule'' guidance when human efficacy studies are not ethical or feasible.
目前尚无批准的药物或生物制剂可用于治疗埃博拉病毒病(EVD)。文献回顾确定了一份包含 141 种药物的清单,这些药物在动物体内具有初步的体外效力和体内疗效报告,或在 EVD 患者中有临床使用/试验报告。这些药物中的大多数已被美国食品和药物管理局单独批准用于治疗各种非 EVD 疾病。这些药物的抗埃博拉病毒效力数据是从文献和公开可用的数据库中整理出来的,同时还整理了它们各自的生物制药和药代动力学特征。为了促进包括抗埃博拉病毒药物在内的抗病毒药物的开发,重点包括优化暴露-反应关系、设计安全有效的临床给药方案,以实现足够高的临床 C 与血浆蛋白结合校正 EC 比值,以及在动物模型(健康和受影响)和健康志愿者中进行药代动力学研究。当人体疗效研究不道德或不可行时,如美国食品和药物管理局“动物规则”指南中所述,总结了用于人体剂量选择的暴露-反应关系。