Efficacy and safety of Abdala COVID-19 subunit vaccine in children and adolescents: An open-label, single-arm, phase 2 trial (MEÑIQUE)

IF 4.5 3区 医学 Q2 IMMUNOLOGY
{"title":"Efficacy and safety of Abdala COVID-19 subunit vaccine in children and adolescents: An open-label, single-arm, phase 2 trial (MEÑIQUE)","authors":"","doi":"10.1016/j.vaccine.2024.126223","DOIUrl":null,"url":null,"abstract":"<div><p><strong>Objectives</strong> We evaluated the safety, immunogenicity and efficacy of Abdala, a protein subunit vaccine for 2019 coronavirus disease (COVID-19), in children and adolescents. <strong>Methods</strong> A phase 2, open-label, single-arm clinical trial was carried out. Subjects aged 3 to 18 years were eligible. Abdala vaccine was administered intramuscularly at 0–14-28 days. The main endpoints were safety and the immunobridging analysis with a non-inferiority design, to infer the efficacy of the vaccine in paediatric population based on the comparison of neutralizing antibodies (NAb) to SARS-CoV-2, with adults (19–21 years). The trial is registered with the Cuban Public Registry of Clinical Trials, RPCEC00000390. <strong>Results</strong> From September 13th to September 17th, 2021, 703 participants were included in the context of a predominantly SARS-CoV-2 Delta variant circulation. The number of individuals who experienced adverse reactions was 264/703 (37·6%). Adverse reactions were mostly mild and occurred at the injection site, which resolved within the first 24–48 h. There were no reports of severe adverse events. For the non-inferiority comparison of 297 children (3–11 years) with 297 adults, the geometric mean (GMT) ratio of SARS-CoV-2 NAb was 0·87 (95% CI 0·69–1·08) and 1·07 (0·82–1·39) in the same comparison for 203 adolescents (12–18 years) and 203 adults. For both age groups, the lower limit of GMT was higher than 0·67. The differences in seroresponse rates of Nab for children were 1% (−2%, 4%) and −3% (−7%, 1%) for adolescents, higher than −10% in both age groups. <strong>Conclusions</strong> The Abdala vaccine was safe and immunogenic in a paediatric population aged 3–18 years, with inferred efficacy based on non-inferior analysis. The vaccine is very suitable to fit into massive vaccination strategies, considering the advantages of using the same vaccine strength (RBD 50 μg) and schedule of administration for both adults and children, as well as the easy storage and handling conditions at 2–8 °C.</p></div>","PeriodicalId":23491,"journal":{"name":"Vaccine","volume":null,"pages":null},"PeriodicalIF":4.5000,"publicationDate":"2024-08-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S0264410X24009058/pdfft?md5=0ab51831eaa0271fa3a82358fc91e23e&pid=1-s2.0-S0264410X24009058-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Vaccine","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0264410X24009058","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Objectives We evaluated the safety, immunogenicity and efficacy of Abdala, a protein subunit vaccine for 2019 coronavirus disease (COVID-19), in children and adolescents. Methods A phase 2, open-label, single-arm clinical trial was carried out. Subjects aged 3 to 18 years were eligible. Abdala vaccine was administered intramuscularly at 0–14-28 days. The main endpoints were safety and the immunobridging analysis with a non-inferiority design, to infer the efficacy of the vaccine in paediatric population based on the comparison of neutralizing antibodies (NAb) to SARS-CoV-2, with adults (19–21 years). The trial is registered with the Cuban Public Registry of Clinical Trials, RPCEC00000390. Results From September 13th to September 17th, 2021, 703 participants were included in the context of a predominantly SARS-CoV-2 Delta variant circulation. The number of individuals who experienced adverse reactions was 264/703 (37·6%). Adverse reactions were mostly mild and occurred at the injection site, which resolved within the first 24–48 h. There were no reports of severe adverse events. For the non-inferiority comparison of 297 children (3–11 years) with 297 adults, the geometric mean (GMT) ratio of SARS-CoV-2 NAb was 0·87 (95% CI 0·69–1·08) and 1·07 (0·82–1·39) in the same comparison for 203 adolescents (12–18 years) and 203 adults. For both age groups, the lower limit of GMT was higher than 0·67. The differences in seroresponse rates of Nab for children were 1% (−2%, 4%) and −3% (−7%, 1%) for adolescents, higher than −10% in both age groups. Conclusions The Abdala vaccine was safe and immunogenic in a paediatric population aged 3–18 years, with inferred efficacy based on non-inferior analysis. The vaccine is very suitable to fit into massive vaccination strategies, considering the advantages of using the same vaccine strength (RBD 50 μg) and schedule of administration for both adults and children, as well as the easy storage and handling conditions at 2–8 °C.

儿童和青少年接种Abdala COVID-19亚单位疫苗的有效性和安全性:一项开放标签、单臂、2期试验(MEÑIQUE)
目的 我们评估了2019年冠状病毒病(COVID-19)蛋白亚单位疫苗Abdala在儿童和青少年中的安全性、免疫原性和有效性。方法 开展了一项 2 期、开放标签、单臂临床试验。3至18岁的受试者均符合条件。阿布达拉疫苗在0-14-28天进行肌肉注射。主要终点是安全性和免疫桥接分析,采用非劣效性设计,根据 SARS-CoV-2 中和抗体(NAb)与成人(19-21 岁)的比较,推断疫苗在儿童群体中的疗效。该试验已在古巴临床试验公共登记处(RPCEC00000390)登记。结果 从 2021 年 9 月 13 日至 9 月 17 日,在以 SARS-CoV-2 Delta 变体为主的流行环境中,有 703 人参加了试验。出现不良反应的人数为 264/703 (37-6%)。不良反应大多较轻,发生在注射部位,在最初的 24-48 小时内缓解。在 297 名儿童(3-11 岁)与 297 名成人的非劣效性比较中,203 名青少年(12-18 岁)和 203 名成人的 SARS-CoV-2 NAb 几何平均(GMT)比值分别为 0-87(95% CI 0-69-1-08)和 1-07(0-82-1-39)。两个年龄组的 GMT 下限均高于 0-67。儿童的纳布血清反应率为 1%(-2%,4%),青少年为-3%(-7%,1%),两个年龄组的差异均高于-10%。结论 阿布达拉疫苗在 3-18 岁的儿童群体中安全且具有免疫原性,根据非劣效性分析推断其有效性。考虑到成人和儿童使用相同的疫苗强度(RBD 50 μg)和给药时间,以及在 2 - 8 °C 下易于储存和处理的优势,该疫苗非常适合大规模疫苗接种策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Vaccine
Vaccine 医学-免疫学
CiteScore
8.70
自引率
5.50%
发文量
992
审稿时长
131 days
期刊介绍: Vaccine is unique in publishing the highest quality science across all disciplines relevant to the field of vaccinology - all original article submissions across basic and clinical research, vaccine manufacturing, history, public policy, behavioral science and ethics, social sciences, safety, and many other related areas are welcomed. The submission categories as given in the Guide for Authors indicate where we receive the most papers. Papers outside these major areas are also welcome and authors are encouraged to contact us with specific questions.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信