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A Phase IIa double-blind, randomised, placebo controlled study of the immunogenicity, safety, tolerability and reactogenicity of three doses of oral RV3-BB Rotavirus Vaccine, with the first dose of vaccine administered either at birth (0-5 days of age) or in infancy.

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A Phase IIa double-blind, randomised, placebo controlled study of the immunogenicity, safety, tolerability and reactogenicity of three doses of oral RV3-BB Rotavirus Vaccine, with the first dose of vaccine administered either at birth (0-5 days of age) or in infancy.

Status: Not yet recruiting
Phase of Trial: Phase II

Latest Information Update: 16 Jul 2019

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