Efficacy and safety of a recombinant hepatitis E vaccine in healthy adults: a large-scale, randomised, double-blind placebo-controlled, phase 3 trial

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	Efficacy and safety of a recombinant hepatitis E vaccine in healthy adults: a large-scale, randomised, double-blind placebo-controlled, phase 3 trial
	Zhu, FC ; Zhang, J ; Zhang, XF ; Zhou, C ; Wang, ZZ ; Huang, SJ ; Wang, H ; Yang, CL ; Jiang, HM ; Cai, JP ; Wang, YJ ; Ai, X ; Hu, YM ; Tang, QA ; Yao, X ; Yan, QA ; Xian, YL ; Wu, T ; Li, YM ; Miao, J ; Ng, MH ; Shih, J
刊名	http://dx.doi.org/10.1016/S0140-6736(10)61030-6
	2010-09-11
关键词	CHRONIC LIVER-DISEASE E VIRUS-INFECTION VIRAL-HEPATITIS PREGNANCY ZOONOSIS IGG
英文摘要	Chinese Government [2006AA02A209, 2005DFA30820]; Chinese National Key Technologies RD Programme [2009ZX10004-704]; Chinese National Science Fund for Distinguished Young Scholars [30925030]; Fujian Provincial Department of Sciences and Technology [2004YZ01; Background Seroprevalence data suggest that a third of the world's population has been infected with the hepatitis E virus. Our aim was to assess efficacy and safety of a recombinant hepatitis E vaccine, HEV 239 (Hecolin; Xiamen Innovax Biotech, Xiamen, China) in a randomised, double-blind, placebo-controlled, phase 3 trial. Methods Healthy adults aged 16-65 years in, Jiangsu Province, China were randomly assigned in a 1:1 ratio to receive three doses of HEV 239 (30 jig of purified recombinant hepatitis E antigen adsorbed to 0.8 mg aluminium hydroxide suspended in 0.5 mL buffered saline) or placebo (hepatitis B vaccine) given intramuscularly at 0, 1, and 6 months. Randomisation was done by computer-generated permuted blocks and stratified by age and sex. Participants were followed up for 19 months. The primary endpoint was prevention of hepatitis E during 12 months from the 31st day after the third dose. Analysis was based on participants who received all three doses per protocol. Study participants, care givers, and investigators were all masked to group and vaccine assignments. This trial is registered with ClinicalTrials.gov, number NCT01014845. Findings 11165 of the trial participants were tested for hepatitis E virus IgG, of which 5285 (47%) were seropositive for hepatitis E virus. Participants were randomly assigned to vaccine (n=56302) or placebo (n=56302). 48 693 (86%) participants in the vaccine group and 48 663 participants (86%) in the placebo group received three vaccine doses and were included in the primary efficacy analysis. During the 12 months after 30 days from receipt of the third dose 15 per-protocol participants in the placebo group developed hepatitis E compared with none in the vaccine group. Vaccine efficacy after three doses was 100.0% (95% CI 72.1-100.0). Adverse effects attributable to the vaccine were few and mild. No vaccination-related serious adverse event was noted. Interpretation HEV 239 is well tolerated and effective in the prevention of hepatitis E in the general population in China, including both men and women age 16-65 years.
语种	英语
内容类型	期刊论文
源URL	[http://dspace.xmu.edu.cn/handle/2288/65099]
专题	生命科学－已发表论文
推荐引用方式 GB/T 7714	Zhu, FC,Zhang, J,Zhang, XF,et al. Efficacy and safety of a recombinant hepatitis E vaccine in healthy adults: a large-scale, randomised, double-blind placebo-controlled, phase 3 trial[J]. http://dx.doi.org/10.1016/S0140-6736(10)61030-6,2010.
APA	Zhu, FC.,Zhang, J.,Zhang, XF.,Zhou, C.,Wang, ZZ.,...&Shih, J.(2010).Efficacy and safety of a recombinant hepatitis E vaccine in healthy adults: a large-scale, randomised, double-blind placebo-controlled, phase 3 trial.http://dx.doi.org/10.1016/S0140-6736(10)61030-6.
MLA	Zhu, FC,et al."Efficacy and safety of a recombinant hepatitis E vaccine in healthy adults: a large-scale, randomised, double-blind placebo-controlled, phase 3 trial".http://dx.doi.org/10.1016/S0140-6736(10)61030-6 (2010).