Morioka Ichiro, Kakei Yasumasa, Omori Takashi, Nozu Kandai, Fujioka Kazumichi, Yoshikawa Tetsushi, Moriuchi Hiroyuki, Ito Yoshinori, Oka Akira
Department of Pediatrics and Child Health, Nihon University School of Medicine.
Department of Oral and Maxillofacial Surgery.
Medicine (Baltimore). 2020 Apr;99(17):e19765. doi: 10.1097/MD.0000000000019765.
Congenital cytomegalovirus (CMV) disease, a common mother-to-child infection, can lead to neurological sequelae. Some clinical trials have shown that oral valganciclovir (VGCV) can improve hearing and neurodevelopmental impairment in infants with congenital CMV disease. However, VGCV has neither been approved in Japan nor other countries as a treatment for this disease by the government health insurance.
This study is a non-randomized, prospective, open-label, multicenter, single-arm clinical trial and will include subjects meeting the following criteria: confirmation of positive CMV-DNA amplification in urine by an in vitro diagnostic test within 21 days of age; congenital CMV disease with one or more central nervous system disorders-microcephaly, hydrocephalus or ventricular enlargement, periventricular calcification, cortical hypoplasia or white matter injury, retinal choroiditis, and abnormal auditory brainstem response (ABR); and infants within 2 months of age with a gestational age ≥32 weeks at birth and weighing ≥1800 g at the time of registration. Subjects will be orally administered 16 mg/kg VGCV twice daily for 6 months. The target number of cases for enrollment between February 3, 2020 and July 31, 2021 is 25. Primary endpoint is the change in whole blood CMV loads before and after 6 months of treatment. The important secondary endpoint is the change in ABR (both best and total ear hearing assessments) before and after 6 months of treatment. The safety endpoints are adverse events and drug side effects.
To the best of our knowledge, this multicenter, open-label, single-arm study will be the first well-designed clinical trial to evaluate the efficacy of oral VGCV in infants with congenital CMV diseases. The findings will reveal the efficacy and safety of oral VGCV treatments and enable the approval of oral VGCV as a treatment for infants with congenital CMV disease by the government health insurance of Japan.
先天性巨细胞病毒(CMV)疾病是一种常见的母婴感染疾病,可导致神经后遗症。一些临床试验表明,口服缬更昔洛韦(VGCV)可改善先天性CMV疾病婴儿的听力和神经发育障碍。然而,VGCV在日本及其他国家均未获得政府医疗保险批准用于治疗该疾病。
本研究为非随机、前瞻性、开放标签、多中心、单臂临床试验,将纳入符合以下标准的受试者:年龄在21天内通过体外诊断试验确认尿中CMV-DNA扩增呈阳性;患有先天性CMV疾病且伴有一种或多种中枢神经系统疾病——小头畸形、脑积水或脑室扩大、脑室周围钙化、皮质发育不全或白质损伤、视网膜脉络膜炎以及听觉脑干反应(ABR)异常;出生时胎龄≥32周且登记时体重≥1800克、年龄在2个月内的婴儿。受试者将每日口服两次16毫克/千克的VGCV,持续6个月。2020年2月3日至2021年7月31日计划纳入的目标病例数为25例。主要终点是治疗6个月前后全血CMV载量的变化。重要的次要终点是治疗6个月前后ABR的变化(最佳和总耳听力评估)。安全性终点是不良事件和药物副作用。
据我们所知,这项多中心、开放标签、单臂研究将是第一项精心设计的临床试验,旨在评估口服VGCV治疗先天性CMV疾病婴儿的疗效。研究结果将揭示口服VGCV治疗的疗效和安全性,并使口服VGCV能够获得日本政府医疗保险批准用于治疗先天性CMV疾病婴儿。