de Bruijn I A, Nauta J, Gerez L, Palache A M
Solvay Pharmaceuticals BV, Clinical Development, P.O. Box 900, 1380 DA Weesp, The Netherlands.
Virus Res. 2004 Jul;103(1-2):139-45. doi: 10.1016/j.virusres.2004.02.026.
In 14 clinical studies, various efficacy and safety aspects of a new virosomal influenza vaccine (Invivac) were assessed in 2865 subjects. The virosomal influenza vaccine fully complies with the Committee for Proprietary Medicinal Products (CPMP) requirement for immunogenicity of influenza vaccines. In particular, in a subset of subjects with low pre-vaccination titers (thus those persons who actually need protection by a vaccine), between 76 and 99% of subjects (dependent on age, health status and vaccine components) achieved protective hemagglutination inhibiting (HI) antibody titers after vaccination with the virosomal influenza vaccine. Acceptable frequencies of well-known local and systemic reactions were observed in healthy adults and risk subjects in clinical studies and in a post-marketing study population. These reactions were transient and generally not severe, and did not cause major inconvenience. In conclusion, Invivac is an efficacious and safe vaccine for the protection against influenza in healthy and chronically ill adult subjects. The vaccine is especially efficacious in subjects with low pre-vaccination immunity.
在14项临床研究中,对2865名受试者评估了一种新型脂质体流感疫苗(英维沃克)的各种有效性和安全性。该脂质体流感疫苗完全符合专利药品委员会(CPMP)对流感疫苗免疫原性的要求。特别是,在接种疫苗前滴度较低的一部分受试者(即那些实际需要疫苗保护的人群)中,76%至99%的受试者(取决于年龄、健康状况和疫苗成分)在接种脂质体流感疫苗后达到了保护性血凝抑制(HI)抗体滴度。在临床研究以及上市后研究人群中的健康成年人和高危受试者中,观察到了常见局部和全身反应的可接受频率。这些反应是短暂的,通常不严重,不会造成重大不便。总之,英维沃克是一种有效且安全的疫苗,可用于保护健康和慢性病成年受试者预防流感。该疫苗在接种前免疫力较低的受试者中尤其有效。