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A Study of Two Doses of Oral Cholera Vaccine (Shanchol™) in Subjects Aged 1 Year and Older in the Philippines

Cholera Clinical Trial

Official title:
Safety and Immunogenicity of Two Doses of Oral Cholera Vaccine (Shanchol™) in Subjects Aged 1 Year and Older in the Philippines

Clinical Trial Summary

The aim of the study is to generate safety and immunogenicity data with Oral Cholera Vaccine (Shanchol™) in The Philippines

Objectives:

- To describe the safety after each dose of Shanchol vaccine.

- To describe the immunogenicity after each dose of Shanchol vaccine.

Clinical Trial Description

Healthy toddlers, children, adolescents and adults, aged 1 year and older will receive two doses of vaccine 14 days apart, and will be assessed baseline immunogenicity (pre-vaccination), and 14 days after each vaccine dose. Safety data will be collected for 14 days after the first dose and 30 days after the second dose. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01949675
Study type Interventional
Source Sanofi
Contact
Status Completed
Phase Phase 4
Start date March 2014
Completion date August 2015
View Details
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