Clinical Trials Directory

Trials / Unknown

UnknownNCT02339896

Observation Study an Immunogenicity Modified TRC-ID Regimen With CPRV With or Without Rabies Immunoglobulin in Children

Observation an Immunogenicity and Safety Study of Modified TRC-ID Regimen With A New Chromatographically Purified Vero Cell Rabies Vaccine (SPEEDA®) With or Without Rabies Immunoglobulin in Children

Status
Unknown
Phase
Study type
Observational
Enrollment
45 (actual)
Sponsor
Queen Saovabha Memorial Institute · Academic / Other
Sex
All
Age
1 Year – 15 Years
Healthy volunteers
Accepted

Summary

To determine Immunogenicity and Safety Study of Modified TRC-ID Regimen with A New Chromatographically Purified Vero Cell Rabies Vaccine (SPEEDA®) as post exposure rabies intradermal regimen with or without Rabies Immunoglobulin in Children

Detailed description

post exposure rabies vaccination with modified Thai red cross intrademal regimen has been proven to be immunogenic and effection when using purified vero cell vaccine (PVRV) In present, new chromatographically purified vero cell rabies vaccine (SPEEDA), chromatography purifed vero cell derived rabies vaccine, is manufactured by the Liaoning Chengda Biotechnology is available This study has a goal to determine the immunogenicity of speeda when using with post exposure rabies intradermal vaccination with or without rabies immune globulin in children

Conditions

Interventions

TypeNameDescription
BIOLOGICALrabies vaccinerabies vaccine 0.1 ml intradermal two site for 4 times

Timeline

Start date
2014-02-01
Primary completion
2015-03-01
Completion
2016-01-01
First posted
2015-01-16
Last updated
2015-01-16

Source: ClinicalTrials.gov record NCT02339896. Inclusion in this directory is not an endorsement.