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Vaccine ; 29(37): 6335-41, 2011 Aug 26.
Artigo em Inglês | MEDLINE | ID: mdl-21640780

RESUMO

A phase III, randomized, double-blind study evaluated the efficacy, reactogenicity, safety and immunogenicity of a human rotavirus vaccine, RIX4414 in Japanese infants aged 6-14 weeks when administered as two doses (0, 1-month schedule). Efficacy against any and severe rotavirus gastroenteritis leading to medical intervention caused by circulating wild-type rotavirus from two weeks post-Dose 2 until two years of age was 79.3% (95% CI: 60.5-89.8%) and 91.6% (95% CI: 62.4-99.1%), respectively. Solicited, unsolicited symptoms and serious adverse events were reported at a similar frequency in both groups. Serum anti-rotavirus antibody seroconversion rate one-month post-Dose 2 was 85.3% (95% CI: 68.9-95%) in RIXX4414 group. RIX4414 was efficacious, well-tolerated and immunogenic in Japanese infants and introduction of vaccination could help in reducing the disease burden.


Assuntos
Infecções por Rotavirus/imunologia , Infecções por Rotavirus/prevenção & controle , Vacinas contra Rotavirus/efeitos adversos , Vacinas contra Rotavirus/imunologia , Anticorpos Antivirais/sangue , Método Duplo-Cego , Gastroenterite/imunologia , Gastroenterite/prevenção & controle , Gastroenterite/virologia , Humanos , Esquemas de Imunização , Japão , Rotavirus/imunologia , Vacinas Atenuadas/efeitos adversos , Vacinas Atenuadas/imunologia
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