Institute of Biological Psychiatry, Mental Health Centre Sct. Hans, Roskilde, Denmark.
Department of Science and Environment, Roskilde University Center, Roskilde, Denmark.
Pharmacol Res Perspect. 2022 Apr;10(2):e00945. doi: 10.1002/prp2.945.
GS-441524, the parent nucleoside of remdesivir, has been proposed to be effective against Covid-19 based on in vitro studies and studies in animals. However, randomized clinical trials of the agent to treat Covid-19 have not been conducted. Here, we evaluated GS-441524 for Covid-19 treatment based on studies reporting pharmacokinetic parameters of the agent in mice, rats, cats, dogs, monkeys, and the single individual in the first-in-human trial supplemented with information about its activity against severe acute respiratory syndrome coronavirus 2 and safety. A dosing interval of 8 h was considered clinically relevant and used to calculate steady-state plasma concentrations of GS-441524. These ranged from 0.27 to 234.41 μM, reflecting differences in species, doses, and administration routes. Fifty percent maximal inhibitory concentrations of GS-441524 against severe acute respiratory syndrome coronavirus 2 ranged from 0.08 μM to above 10 μM with a median of 0.87 μM whereas concentrations required to produce 90% of the maximal inhibition of the virus varied from 0.18 µM to more than 20 µM with a median of 1.42 µM in the collected data. Most of these concentrations were substantially lower than the calculated steady-state plasma concentrations of the agent. Plasma exposures to orally administered GS-441524, calculated after normalization of doses, were larger for dogs, mice, and rats than cynomolgus monkeys and humans, probably reflecting interspecies differences in oral uptake with reported oral bioavailabilities below 8.0% in cynomolgus monkeys and values as high as 92% in dogs. Reported oral bioavailabilities in rodents ranged from 12% to 57%. Using different presumptions, we estimated human oral bioavailability of GS-441524 at 13% and 20%. Importantly, doses of GS-441524 lower than the 13 mg/kg dose used in the first-in-human trial may be effective against Covid-19. Also, GS-441524 appears to be well-tolerated. In conclusion, GS-441524 has potential for oral treatment of Covid-19.
瑞德西韦的前体核苷 GS-441524,基于体外研究和动物研究,被提议对新冠病毒有效。然而,针对新冠病毒的该药物的随机临床试验尚未进行。在此,我们根据报告了该药物在小鼠、大鼠、猫、狗、猴子和首个人体试验中个体的药代动力学参数的研究,以及关于其对严重急性呼吸综合征冠状病毒 2 的活性和安全性的信息,评估了 GS-441524 用于新冠病毒治疗。8 小时的给药间隔被认为具有临床相关性,并用于计算 GS-441524 的稳态血浆浓度。这些浓度范围从 0.27 到 234.41 μM,反映了物种、剂量和给药途径的差异。GS-441524 对严重急性呼吸综合征冠状病毒 2 的 50%最大抑制浓度范围为 0.08 μM 至超过 10 μM,中位数为 0.87 μM,而产生病毒最大抑制的 90%所需浓度在收集的数据中范围从 0.18 μM 至超过 20 μM,中位数为 1.42 μM。这些浓度中的大多数都明显低于计算出的该药物的稳态血浆浓度。经归一化剂量后,口服给予 GS-441524 的血浆暴露量,在狗、小鼠和大鼠中大于食蟹猴和人类,可能反映了口服摄取的种间差异,报道的口服生物利用度在食蟹猴中低于 8.0%,而在狗中高达 92%。在啮齿动物中的报道的口服生物利用度范围从 12%到 57%。使用不同的假设,我们估计 GS-441524 的人类口服生物利用度为 13%和 20%。重要的是,低于首个人体试验中使用的 13 mg/kg 剂量的 GS-441524 可能对新冠病毒有效。此外,GS-441524 似乎耐受性良好。总之,GS-441524 具有治疗新冠病毒的口服潜力。