ID

36624

Descrição

Study ID: 102394 Clinical Study ID: 102394 Study Title: A Phase IV, partially double-blind study to demonstrate non-inferiority of GSK Biologicals’ Mencevax™ ACWY (new process) versus Mencevax™ ACWY (current process) when administered as a single dose to subjects aged 2-30 yrs Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00227422 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 4 Study Recruitment Status: Completed clinical study under GSK sponsorship. The product that is studied in this clinical study, together with the rights to the data and results generated, has been transferred by GSK to Pfizer. GSK’s Clinical Study Register is no longer maintained for this study. To request access to clinical study data from Pfizer, go here: http://www.pfizer.com/research/clinical_trials/trial_data_and_results Generic Name: Meningococcal Serogroups A, C, W-135 and Y Vaccine Trade Name: Mencevax Study Indication: Infections, Meningococcal

Link

http://www.pfizer.com/research/clinical_trials/trial_data_and_results

Palavras-chave

  1. 26/05/2019 26/05/2019 -
Titular dos direitos

GlaxoSmithKline

Transferido a

26 de maio de 2019

DOI

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Licença

Creative Commons BY-NC 3.0

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Mencevax™ ACWY (new process) versus Mencevax™ ACWY (current process); NCT00227422

Concomitant Vaccination

Administrative Data
Descrição

Administrative Data

Alias
UMLS CUI-1
C1320722
Subject Number
Descrição

Clinical Trial Subject Unique Identifier

Tipo de dados

integer

Alias
UMLS CUI [1]
C2348585
Concomitant Vaccination
Descrição

Concomitant Vaccination

Alias
UMLS CUI-1
C2347852
UMLS CUI-2
C0042196
Has any vaccine other than the study vaccine(s) been administered during the timeframe as specified in the Protocol?
Descrição

Concomitant Agent, Vaccination

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C2347852
UMLS CUI [1,2]
C0042196
Trade / (Generic) Name
Descrição

Concomitant Agent, Vaccination, Medication name

Tipo de dados

text

Alias
UMLS CUI [1,1]
C2347852
UMLS CUI [1,2]
C0042196
UMLS CUI [1,3]
C2360065
Route
Descrição

Concomitant Agent, Vaccination, Drug Administration Routes

Tipo de dados

text

Alias
UMLS CUI [1,1]
C2347852
UMLS CUI [1,2]
C0042196
UMLS CUI [1,3]
C0013153
Administration date
Descrição

Concomitant Agent, Vaccination, Date in time

Tipo de dados

date

Alias
UMLS CUI [1,1]
C2347852
UMLS CUI [1,2]
C0042196
UMLS CUI [1,3]
C0011008

Similar models

Concomitant Vaccination

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
Administrative Data
C1320722 (UMLS CUI-1)
Clinical Trial Subject Unique Identifier
Item
Subject Number
integer
C2348585 (UMLS CUI [1])
Item Group
Concomitant Vaccination
C2347852 (UMLS CUI-1)
C0042196 (UMLS CUI-2)
Concomitant Agent, Vaccination
Item
Has any vaccine other than the study vaccine(s) been administered during the timeframe as specified in the Protocol?
boolean
C2347852 (UMLS CUI [1,1])
C0042196 (UMLS CUI [1,2])
Concomitant Agent, Vaccination, Medication name
Item
Trade / (Generic) Name
text
C2347852 (UMLS CUI [1,1])
C0042196 (UMLS CUI [1,2])
C2360065 (UMLS CUI [1,3])
Concomitant Agent, Vaccination, Drug Administration Routes
Item
Route
text
C2347852 (UMLS CUI [1,1])
C0042196 (UMLS CUI [1,2])
C0013153 (UMLS CUI [1,3])
Concomitant Agent, Vaccination, Date in time
Item
Administration date
date
C2347852 (UMLS CUI [1,1])
C0042196 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])

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