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Bharat Biotech successfully completes 116E Rotavirus vaccine phase I&II trials
Our Bureau, Hyderabad | Thursday, May 29, 2008, 08:00 Hrs  [IST]

The Indian Rotavirus Vaccine Development Project (RVDP) announced encouraging results of a recent phase I/II clinical trial of a live, natural reassortant, oral rotavirus vaccine 116E (ORV 116E), conducted in New Delhi.

RVDP is a collaborative effort with support and guidance from the Department of Biotechnology, PATH, US Centers for Disease Control and Prevention (CDC), Stanford University, US National Institutes of Health, National Institute of Allergy and Infectious Diseases (NIAID), Society for Applied Studies; National Institute of Immunology, New Delhi, Indo-US Vaccine Action Programme, All India Institute of Medical Sciences and Bharat Biotech International Ltd.

Rotavirus infections are the single largest cause of severe diarrhoea disease among infants and children worldwide and cause more than 500,000 deaths in infants and children each year, with 90 per cent of these deaths occurring in the world's poorest countries. Rotavirus diarrhoea causes more than 120,000 deaths in India alone.

The phase I/II trial was designed as a double-blind randomized placebo controlled dose escalating study of ORV 116E in healthy non-malnourished infants 8-20 weeks of age with safety and immunogenicity as the primary and secondary objectives, respectively. The study was conducted by the society for applied studies in New Delhi.

The doses selected for administration were 104.0 and 105.0 FFU with reactogenicity, immunogenicity and viral shedding as the study endpoints. One-hundred and eighty-seven infants were enrolled for the 104.0 FFU dosage and 182 were enrolled for the 105.0 FFU dosage.

ORV 116E was well tolerated after three administrations with no differences observed in mild, moderate or severe adverse events among vaccine and placebo recipients in both the 104.0 and 105.0 FFU dosages. ORV 116E was immunogenic with 62.1 per cent and 89.7 per cent of the infants seroconverting after three doses of the 104.0 and 105.0 FFU dosages, respectively. These favourable early clinical results are encouraging and warrant further development of ORV 116E as a new rotavirus vaccine for young infants in developing world settings.

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