ID
33079
Description
Study ID: 104020 Clinical Study ID: 104020 Study Title: Blinded, randomised study to assess the immunogenicity and safety of GlaxoSmithKline (GSK) Biologicals’ live attenuated measles-mumps-rubella-varicella candidate vaccine when given to healthy children in their second year of life Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00126997 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 4 Study Recruitment Status: Completed Generic Name: Combined Measles, Mumps, Rubella, Varicella Vaccine Trade Name: Priorix Tetra Study Indication: Measles; Mumps; Rubella; Varicella
Keywords
Versions (1)
- 11/26/18 11/26/18 -
Copyright Holder
GSK group of companies
Uploaded on
November 26, 2018
DOI
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License
Creative Commons BY-NC 3.0
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Immunogenicity of Combined Measles, Mumps, Rubella, Varicella Vaccine for healthy 2 y.o children - 104020
Concomitant Vaccination Form
- StudyEvent: ODM
Description
Concomitant Vaccination
Description
Has any vaccine other than the study vaccine(s) been administered during the timeframe as specified in the protocol?
Data type
boolean
Description
If Yes, please record concomitant vaccination with trade name and /or generic name, route and vaccine administration date
Data type
text
Description
Trade Name / Generic Name
Description
Trade / Generic Name
Data type
text
Description
Route
Data type
text
Description
Administration Date
Data type
date
Similar models
Concomitant Vaccination Form
- StudyEvent: ODM
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