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Clinical trial

A Phase II, Randomized, Double-blind, Vaccine-controlled Dose-escalating Study to Evaluate the Immunogenicity, Reactogenicity and Safety of Oral Live Attenuated Human Rotavirus (HRV) Vaccine (Rotavin-M1) in Healthy Infants in Vietnam

NCT01377571 is registered in ClinicalTrials.gov with National Institute of Hygiene and Epidemiology, Vietnam as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
A Phase II, Randomized, Double-blind, Vaccine-controlled Dose-escalating Study to Evaluate the Immunogenicity, Reactogenicity and Safety of Oral Live Attenuated Human Rotavirus (HRV) Vaccine (Rotavin-M1) in Healthy Infants in Vietnam
Lead sponsor
National Institute of Hygiene and Epidemiology, Vietnam
Phase
Phase 2
Overall status
Completed
Start date
October 31, 2009
Completion date
April 30, 2010
Enrollment
200 (actual)
Sites
1

Conditions

As the registry lists them; a condition with its own page is linked.

diarrhea, fever, irritability, nausea, vomit