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Original Article
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Volume 356:895-903 March 1, 2007 Number 9
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Safety and Efficacy of a Recombinant Hepatitis E Vaccine
Mrigendra Prasad Shrestha, M.B., B.S., Robert McNair Scott, M.D., Durga Man Joshi, M.D., Mammen P. Mammen, Jr., M.D., Gyan Bahadur Thapa, M.B., B.S., Narbada Thapa, Ph.D., Khin Saw Aye Myint, M.B., B.S., Marc Fourneau, B.S., Robert A. Kuschner, M.D., Sanjaya Kumar Shrestha, M.D., Marie Pierre David, M.S., Jitvimol Seriwatana, M.S., David W. Vaughn, M.D., Assad Safary, M.D., Timothy P. Endy, M.D., and Bruce L. Innis, M.D.

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ABSTRACT

Background Hepatitis E virus (HEV) is an important cause of viral hepatitis. We evaluated the safety and efficacy of an HEV recombinant protein (rHEV) vaccine in a phase 2, randomized, double-blind, placebo-controlled trial.

Methods In Nepal, we studied 2000 healthy adults susceptible to HEV infection who were randomly assigned to receive three doses of either the rHEV vaccine or placebo at months 0, 1, and 6. Active (including hospital) surveillance was used to identify acute hepatitis and adverse events. The primary end point was the development of hepatitis E after three vaccine doses.

Results A total of 1794 subjects (898 in the vaccine group and 896 in the placebo group) received three vaccine doses; the total vaccinated cohort was followed for a median of 804 days. After three vaccine doses, hepatitis E developed in 69 subjects, of whom 66 were in the placebo group. The vaccine efficacy was 95.5% (95% confidence interval [CI], 85.6 to 98.6). In an intention-to-treat analysis that included all 87 subjects in whom hepatitis E developed after the first vaccine dose, 9 subjects were in the vaccine group, with a vaccine efficacy of 88.5% (95% CI, 77.1 to 94.2). Among subjects in a subgroup randomly selected for analysis of injection-site findings and general symptoms (reactogenicity subgroup) during the 8-day period after the administration of any dose, the proportion of subjects with adverse events was similar in the two study groups, except that injection-site pain was increased in the vaccine group (P=0.03).

Conclusions In a high-risk population, the rHEV vaccine was effective in the prevention of hepatitis E. (ClinicalTrials.gov number, NCT00287469 [ClinicalTrials.gov] .)


Source Information

From the Walter Reed–Armed Forces Research Institute of Medical Sciences Research Unit Nepal (M.P.S., R.M.S., S.K.S.) and the Nepalese Army (D.M.J., G.B.T., N.T.) — both in Kathmandu, Nepal; the Armed Forces Research Institute of Medical Sciences, Bangkok, Thailand (M.P.M., K.S.A.M., T.P.E.); GlaxoSmithKline Biologicals, Rixensart, Belgium (M.F., M.P.D., A.S.) and King of Prussia, PA (B.L.I.); and the Walter Reed Army Institute of Research, Silver Spring (R.A.K., J.S., D.W.V., T.P.E.), and the Military Infectious Diseases Research Program, Army Medical Research and Materiel Command, Fort Detrick (D.W.V.) — both in Maryland.

Address reprint requests to Dr. Innis at GlaxoSmithKline, 2301 Renaissance Blvd., King of Prussia, PA 19406-2772, or at bruce.2.innis{at}gsk.com.

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Related Letters:

Hepatitis E Vaccine
Basu S., Lurie P., Bhattarai A., Innis B. L., Shrestha M. P., Scott R. M.
Extract | Full Text | PDF  
N Engl J Med 2007; 356:2421-2422, Jun 7, 2007. Correspondence

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