ID
26863
Beskrivning
Study ID: 103533 Clinical Study ID: 103533 Study Title: Evaluate the immunogenicity, reactogenicity, safety of 4 different formulations of GSK Biologicals' conjugate vaccine (MenACWY) vs 1 dose of MenC-CRM197 or Mencevax™ ACWY in children aged 12-14 months & 3-5 years Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00196976 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 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 GSK’s Clinical Study Register is no longer maintained for this study.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-Tetanus Toxoid Conjugate Vaccine Trade Name: Nimenrix Study Indication: Infections, Meningococcal
Länk
http://www.pfizer.com/research/clinical_trials/trial_data_and_results
Nyckelord
Versioner (1)
- 2017-10-26 2017-10-26 -
Rättsinnehavare
Pfizer
Uppladdad den
26 oktober 2017
DOI
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Licens
Creative Commons BY-NC 3.0
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Meningococcal Infections Vaccination in children NCT00196976
Visit 2 Part 1
- StudyEvent: ODM
Beskrivning
Study Continuation
Alias
- UMLS CUI-1
- C0008972 (Clinical Research)
- UMLS CUI-2
- C0805733 (Continuation status)
- LOINC
- MTHU008303
Beskrivning
Subject return to visit
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C0545082 (Visit)
- UMLS CUI [1,2]
- C0805733 (Continuation status)
- LOINC
- MTHU008303
- UMLS CUI [1,3]
- C0008976 (Clinical Trials)
- SNOMED
- 110465008
- LOINC
- LP231796-6
Beskrivning
Reason no study continuation
Datatyp
text
Alias
- UMLS CUI [1,1]
- C0008972 (Clinical Research)
- UMLS CUI [1,2]
- C0805733 (Continuation status)
- LOINC
- MTHU008303
Beskrivning
Serious adverse event Number | Unsolicited Adverse Event Number | Solicited Adverse Event code
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C1519255 (Serious Adverse Event)
- UMLS CUI [1,2]
- C0805701 (Code)
- UMLS CUI [1,3]
- C1521902 (To specify)
- UMLS CUI [2,1]
- C0877248 (Adverse event)
- LOINC
- MTHU014542
- UMLS CUI [2,2]
- C0805701 (Code)
- UMLS CUI [2,3]
- C1521902 (To specify)
Beskrivning
Decision
Datatyp
text
Alias
- UMLS CUI [1]
- C0679006 (Decision)
Beskrivning
LABORATORY TESTS; BLOOD SAMPLE
Alias
- UMLS CUI-1
- C0022885 (Laboratory Procedures)
- SNOMED
- 269814003
- UMLS CUI-2
- C0005834 (Collection of blood specimen for laboratory procedure)
- SNOMED
- 82078001
- LOINC
- LP125037-4
Beskrivning
Blood sample taken
Datatyp
boolean
Alias
- UMLS CUI [1]
- C1277698 (Blood sample taken)
- SNOMED
- 313334002
Beskrivning
Date
Datatyp
date
Alias
- UMLS CUI [1,1]
- C0011008 (Date in time)
- SNOMED
- 410671006
- UMLS CUI [1,2]
- C0005834 (Collection of blood specimen for laboratory procedure)
- SNOMED
- 82078001
- LOINC
- LP125037-4
Similar models
Visit 2 Part 1
- StudyEvent: ODM
C0805733 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
C0805733 (UMLS CUI [1,2])
C0805701 (UMLS CUI [1,2])
C1521902 (UMLS CUI [1,3])
C0877248 (UMLS CUI [2,1])
C0805701 (UMLS CUI [2,2])
C1521902 (UMLS CUI [2,3])
C0005834 (UMLS CUI-2)
C0005834 (UMLS CUI [1,2])
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