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Safety of two doses of an inactivated hepatitis a vaccine given 6 months apart in healthy toddlers, children, and adolescents aged 12 months to 15 years in China: a phase IV study

机译:两种剂量的灭活丙型肝炎的安全性在12个月至15年龄为15年的健康小孩,儿童和青少年的6个月内给予6个月:第四阶段研究

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Hepatitis A is a vaccine-preventable infection caused by the HA virus (HAV) with transitional to intermediate endemicity in China. An inactivated vaccine first licensed in China in 2010 (Avaxim (R) 80U Pediatric) is indicated for primary and booster vaccination in children from 12 months to 15 years of age. This Phase IV, open-label, single-arm trial supported licensure in pediatric age groups in China. A total of 355 healthy infants and toddlers ( = 12 years of age) were enrolled to receive two doses of intramuscular HA vaccine, separated by 6 months. Participants were split into Group 1 (infants and toddlers: N = 270) and Group 2 (children and adolescents: N = 85). Safety was assessed by solicited injection site and systemic adverse events (AEs) for 7 days and unsolicited AEs for 30 days after each vaccination. Serious AEs (SAEs) were collected throughout. Immunogenicity was not assessed. Analyses were descriptive. Both vaccinations were very well tolerated in each group. The incidence of solicited injection site reactions was lower in Group 1 (17.9%) than Group 2 (33.3%) and for solicited systemic reactions was similar for each group. The incidence of unsolicited AEs in Group 1 was 6.3% and none in Group 2. For solicited and unsolicited AEs the incidence was slightly higher after the first vaccination. There were no SAEs. Overall, the good safety profile of this pediatric HA vaccine was confirmed in infants, toddlers, children, and adolescents aged 12 months to 15 years in China.
机译:甲型肝炎是由HA病毒(HAV)引起的疫苗可预防的感染,其在中国中间人的流行性。 2010年在中国的灭活疫苗(Avaxim(R)80U儿科)被指示为12个月至15岁儿童的初级和加强疫苗接种。该第四级,开放式标签,单臂试验支持在中国儿科年龄群体的许可证。共有355名健康婴儿和幼儿(= 12岁),注册了两剂肌内HA疫苗,以6个月分开。参与者分为第1组(婴儿和幼儿:n = 270)和第2组(儿童和青少年:n = 85)。通过征集注射部位和全身不良事件(AES)评估安全性7天和每次疫苗后30天内未经请求的AES。始终收集严重的AES(SAES)。未评估免疫原性。分析是描述性的。在每组中,两种疫苗均耐受。征收注射部位反应的发病率低于第1(17.9%),比2(33.3%),每组征集的全身反应相似。第1组未经请求的AES的发病率为6.3%,第2组中没有。对于第一次疫苗接种后,征集和未经请求的AES的发病率略高。没有Saes。总体而言,在12个月至15年的婴儿,小孩,儿童和青少年中确认了这种儿科医管局疫苗的良好安全性曲线。

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