Superior immunogenicity of high-dose quadrivalent inactivated influenza vaccine versus Standard-Dose vaccine in Japanese Adults? 60 years of age: Results from a phase III, randomized clinical trial

被引:4
作者
Sanchez, Leilani [1 ]
Nakama, Takahiro [2 ,8 ]
Nagai, Hideaki [3 ]
Matsuoka, Osamu [4 ]
Inoue, Satoshi [5 ]
Inoue, Takahiro [2 ,9 ]
Shrestha, Anju [6 ,10 ]
Pandey, Aseem [6 ]
Chang, Lee-Jah [6 ,11 ]
De Bruijn, Iris [7 ]
机构
[1] Sanofi, Taguig, Philippines
[2] Sanofi KK, Tokyo, Japan
[3] Tokyo Natl Hosp, Natl Hosp Org, Dept Infect Dis, Tokyo, Japan
[4] Med Corp Heishinkai ToCROM Clin, Tokyo, Japan
[5] Med Corp Heishinkai OCROM Clin, Osaka, Japan
[6] Sanofi, Swiftwater, PA USA
[7] Sanofi, Marcy Letoile, France
[8] Janssen Pharmaceut KK, Tokyo, Japan
[9] Astellas Pharm, Tokyo, Japan
[10] Regeneron Pharmaceut, Basking Ridge, NJ USA
[11] AstraZeneca, Gaithersburg, MD USA
关键词
Immunogenicity; Safety; High-dose quadrivalent influenza vaccine; Older adults; Clinical study; Japan; OLDER-ADULTS; EFFICACY;
D O I
10.1016/j.vaccine.2023.02.071
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: A high-dose, split-virion inactivated quadrivalent influenza vaccine (IIV4-HD; Sanofi) is being used for the prevention of influenza in multiple countries. This study examined the immunogenic-ity and safety of the IIV4-HD vaccine administered intramuscularly (IM) compared with a locally licensed standard-dose influenza vaccine (IIV4-SD) administered subcutaneously (SC) in Japan. Methods: This was a phase III, randomized, modified double-blind, active-controlled, multi-center study in older adults >= 60 years of age conducted during the Northern Hemisphere (NH) influenza season of 2020-21 in Japan. Participants were randomized in a 1:1 ratio to receive a single IM injection of IIV4-HD or SC injection of IIV4-SD. Hemagglutination inhibition antibody and seroconversion rates were mea-sured at baseline and day 28. Solicited reactions were collected for up to 7 days after vaccination, unso-licited adverse events up to 28 days after vaccination, and serious adverse events throughout the study. Results: The study included 2100 adults >= 60 years of age. IIV4-HD given IM induced superior immune responses versus IIV4-SD given SC as assessed by geometric mean titers for all four influenza strains. Superior seroconversion rates were also observed for IIV4-HD compared to IIV4-SD for all influenza strains. The safety profiles of IIV4-HD and IIV4-SD were similar. IIV4-HD was well tolerated in partici-pants, with no safety concerns identified. Conclusions: IIV4-HD provided superior immunogenicity versus IIV4-SD and was well tolerated in participants >= 60 years of age in Japan. With superior immunogenicity based on the multiple randomized controlled trials and real-world evidence of trivalent high-dose formulation, IIV4-HD is expected to be the first differentiated influenza vaccine in Japan that offer a greater protection against influenza and its complications in adults 60 years of age and older. Study registration: NCT04498832 (clinicaltrials.gov); U1111-1225-1085 (who.int).(c) 2023 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:2553 / 2561
页数:9
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