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Safety and immunogenicity of the modified adult tick-borne encephalitis vaccine FSME-IMMUN: results of two large phase 3 clinical studies

机译:改良的成人tick传脑炎疫苗FSME-IMMUN的安全性和免疫原性:两项大型3期临床研究的结果

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摘要

A prospective, randomised, multicentre, single-blind phase 3 study was performed to assess the safety of a vaccination schedule consisting of two vaccinations (21-35 days apart) with the tick-borne encephalitis (TBE) vaccine FSME-IMMUN "adults" (five consecutive lots) in comparison to another licensed TBE vaccine (Encepur), with polygeline) (two lots) in healthy volunteers (n=3966) aged 16-65 years. The safety of the third vaccination with FSME-IMMUN "adults" (6 months after the first vaccination) was investigated in a follow-up study on the same population (n=3705) and TBE antibody titres were analysed pre- and post-vaccination in a subgroup of volunteers (n=564). Following the first vaccination, the overall incidence of fever (> or =38.0 degrees C) was 0.8% in the FSME-IMMUN "adults" study group and 5.6% in the comparator study group; fever was mainly mild. The fever rate after the second vaccination was 0.6% and 0.5% in the two study groups, respectively. Local and systemic reactions after the first vaccination occurred with a lower frequency in the FSME-IMMUN "adults" study group than in the comparator group. Upon analysing the tolerability of the third vaccination with FSME-IMMUN "adults", similar results were determined in both study groups of volunteers previously vaccinated with FSME-IMMUN "adults" or with the comparator vaccine. The immunogenicity results demonstrated similar seroconversion rates (as determined by ELISA or neutralization test) before and after the third vaccination in the FSME-IMMUN "adults" group and in the comparator group respectively. The results of both studies demonstrate that: (1) FSME-IMMUN "adults" is safe and highly immunogenic, (2) all five production lots of FSME-IMMUN "adults" were consistent with respect to a low rate of adverse events, (3) FSME-IMMUN "adults" induces considerably lower adverse reaction rates than the comparator vaccine after the first vaccination, and (4) two vaccinations with the comparator vaccine can be successfully followed by a third vaccination with FSME-IMMUN "adults".
机译:进行了一项前瞻性,随机,多中心,单盲第3期研究,以评估由schedule传播脑炎(TBE)疫苗FSME-IMMUN“成人”进行的两次接种(相隔21-35天)组成的接种时间表的安全性(连续五批)与另一种许可的TBE疫苗(Encepur)和多吉林(两批)在16-65岁的健康志愿者(n = 3966)中进行比较。在同一人群(n = 3705)的随访研究中,对FSME-IMMUN“成人”进行的第三次疫苗接种的安全性(第一次疫苗接种后6个月)进行了调查,并分析了疫苗接种前后的TBE抗体滴度在一个志愿者小组中(n = 564)。初次接种疫苗后,FSME-IMMUN“成人”研究组的总体发烧(≥38.0摄氏度)为0.8%,对比例研究组为5.6%;发烧主要是轻度的。两个研究组第二次接种疫苗后的发烧率分别为0.6%和0.5%。 FSME-IMMUN“成人”研究组首次接种疫苗后发生局部和全身反应的频率低于比较组。通过分析用FSME-IMMUN“成人”进行的第三次接种的耐受性,在先前接种过FSME-IMMUN“成人”或比较疫苗的两个志愿者研究组中均获得了相似的结果。免疫原性结果表明,分别在FSME-IMMUN“成人”组和比较组中,在第三次接种之前和之后相似的血清转化率(通过ELISA或中和试验确定)。两项研究的结果均表明:(1)FSME-IMMUN“成人”是安全且具有高度免疫原性的;(2)FSME-IMMUN“成人”的所有五个生产批次在不良事件发生率较低方面均保持一致,( 3)FSME-IMMUN“成人”在第一次疫苗接种后的不良反应发生率大大低于比较疫苗,(4)用比较疫苗进行两次疫苗接种后,可以成功进行FSME-IMMUN“成人”的第三次疫苗接种。

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