莫斯诺地韦(JNJ-1802)不同维持剂量方案在健康成人中的药代动力学、安全性和耐受性

IF 1.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Thomas N Kakuda, Nicole Harasym, Annemie Buelens, Ariane Kahnt, Caroline Feys, Ami Nilsson, Nele Goeyvaerts, Tristan Baguet, Tine De Marez, Guillermo Herrera-Taracena, Freya Rasschaert
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引用次数: 0

摘要

登革热病毒感染已成为一个全球卫生问题,目前尚无针对登革热的治疗方法。Mosnodenvir是一种临床开发中的泛血清型登革热抗病毒药物。在这项1期开放标签研究(NCT05201937)中,在每天两次负载剂量(LD)超过2天后,评估了mosnodenvir的高剂量和低剂量每周和每周两次维持剂量(MDs)。探讨了一种简便的毛细管采血装置TASSO-M20的实用性。健康成人依次接受:450毫克每日两次的LD, 900毫克每周一次的MD;450mg每日两次,450mg每日两次;150毫克每日两次,300毫克每日一次;或150mg每日两次LD, 150mg每周两次MD。莫斯诺韦暴露量随LD迅速增加,并在MD期保持。一般来说,mosnodenvir以剂量正比的方式增加,在每周一次和每周两次MD之间,浓度-时间曲线下的面积相似。不同治疗的平均终端消除半衰期为6.7-8.7天,支持较少的给药频率。所有治疗方案的安全性和耐受性相似。参与者更喜欢TASSO-M20而不是静脉穿刺。总而言之,每周或每两周给予莫斯诺地韦的药代动力学暴露是安全且耐受性良好的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pharmacokinetics, Safety, and Tolerability of Different Maintenance Dose Regimens of Mosnodenvir (JNJ-1802) in Healthy Adult Participants.

Dengue virus infection has become a global health concern, and no dengue-specific treatment is available. Mosnodenvir is a pan-serotypic dengue antiviral in clinical development. In this Phase 1, open-label study (NCT05201937), high- and low-dose weekly, and twice weekly maintenance doses (MDs) of mosnodenvir were evaluated following a twice daily loading dose (LD) over 2 days. The utility of a convenient capillary blood sampling device (TASSO-M20) was also explored. Healthy adults were sequentially assigned to receive: 450 mg twice daily LD, 900 mg once weekly MD; 450 mg twice daily LD, 450 mg twice weekly MD; 150 mg twice daily LD, 300 mg once weekly MD; or 150 mg twice daily LD, 150 mg twice weekly MD. Mosnodenvir exposure rapidly increased with LD and was maintained during the MD phase. In general, mosnodenvir increased in a dose-proportional manner with similar areas under the concentration-time curve between once weekly and twice weekly MD. The mean terminal elimination half-life across treatments was 6.7-8.7 days, supporting less frequent dosing. Safety and tolerability were similar across all treatment regimens. TASSO-M20 was preferred over venipuncture by participants. In summary, mosnodenvir administered weekly or biweekly achieved pharmacokinetic exposures that were found to be safe and well tolerated.

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来源期刊
CiteScore
3.70
自引率
10.00%
发文量
154
期刊介绍: Clinical Pharmacology in Drug Development is an international, peer-reviewed, online publication focused on publishing high-quality clinical pharmacology studies in drug development which are primarily (but not exclusively) performed in early development phases in healthy subjects.
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