ID

34703

Descrizione

Study ID: 103974 (primary study) Clinical Study ID: 103974 Study Title: Demonstrate non-inferiority of Men-C immune response of Hib-MenC with Infanrix™-IPV versus a licensed Men-C vaccine with Pediacel™ when given at 2, 3, 4 months and the immunogenicity of Hib-MenC when given as a booster dose at 12-15 months Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00258700 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 3 Study Recruitment Status: Completed Generic Name: Haemophilus influenzae Type b, Meningococcal C-Tetanus Toxoid Conjugate Vaccine Trade Name: BIO HIB-MENC-TT; Menitorix Study Indication: Haemophilus influenzae type b; Neisseria Meningitidis

Keywords

versioni (1)
  1. 23/01/19 23/01/19 -
Titolare del copyright

GSK group of companies

Caricato su

23 gennaio 2019

DOI

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Licenza

Creative Commons BY-NC 3.0
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Study of Long-term Antibody Persistence After a Booster Dose of Menitorix Vaccine - 109664

Inglese

Reason for non participation - Tracking Form + Use of Samples Compliance

1 moduli  
Administrative data
Descrizione

Administrative data

Center Number
Descrizione

Center Number

Tipo di dati

integer

Tracking Document
Descrizione

Tracking Document

Previous Subject Number
Descrizione

Previous study: 109664 (Hib-MenC-TT-027 EXT: 013 M12)

Tipo di dati

integer

Date of Birth
Descrizione

Date of Birth

Tipo di dati

date

Reason for non participation
Descrizione

Reason for non participation

Tipo di dati

text

Please specify criteria that are not fulfilled
Descrizione

IfSubjectNotEligible

Tipo di dati

text

In case of SAE, specify adverse event
Descrizione

SAE

Tipo di dati

text

If Other, please specify
Descrizione

Other

Tipo di dati

text

In case of death, please specify the date
Descrizione

DeathDate

Tipo di dati

date

Date of Contact
Descrizione

Date of Contact

Tipo di dati

date

Investigator Name
Descrizione

Print name

Tipo di dati

text

Signature
Descrizione

Signature

Tipo di dati

text

Date
Descrizione

Date

Tipo di dati

date

Use of Human Samples by GSK
Descrizione

Use of Human Samples by GSK

In addition to the use of samples for the tests described in the protocol, samples might be used for other resarch by GSK (see protocol). Please tick what is also covered by the subject Informed Consent form of your center.
Descrizione

USE OF HUMAN SAMPLES BY GSK

Tipo di dati

text

Please tick below box if a 15 years GSK storage period is covered by the subject’s Informed Consent form of your center.
Descrizione

StoragePeriod

Tipo di dati

text

If Other, please specify
Descrizione

Other

Tipo di dati

text

ICF Effective date
Descrizione

Complete and submit a new form for each change during the study.

Tipo di dati

date

Investigator's Signature
Descrizione

Investigator's Signature

Investigator's signature:
Descrizione

Investigator's signature:

Tipo di dati

text

Date:
Descrizione

Date:

Tipo di dati

date

Printed Investigator's name:
Descrizione

Printed Investigator's name:

Tipo di dati

text

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Similar models

Reason for non participation - Tracking Form + Use of Samples Compliance

1 moduli
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
Administrative data
Center Number
Item
Center Number
integer
Item Group
Tracking Document
Previous Subject Number
Item
Previous Subject Number
integer
Date of Birth
Item
Date of Birth
date
Item
Reason for non participation
text
Reason for non participation
Code List
Reason for non participation
CL Item
Subject not eligible (1)
CL Item
Subject lost to follow-up or not reached (2)
CL Item
Subject eligible but not willing to participate  (3)
CL Item
Subject died (4)
IfSubjectNotEligible
Item
Please specify criteria that are not fulfilled
text
SAE
Item
In case of SAE, specify adverse event
text
Other
Item
If Other, please specify
text
DeathDate
Item
In case of death, please specify the date
date
Date of Contact
Item
Date of Contact
date
Investigator Name
Item
Investigator Name
text
Signature
Item
Signature
text
Date
Item
Date
date
Item Group
Use of Human Samples by GSK
Item
In addition to the use of samples for the tests described in the protocol, samples might be used for other resarch by GSK (see protocol). Please tick what is also covered by the subject Informed Consent form of your center.
text
USE OF HUMAN SAMPLES BY GSK
Code List
In addition to the use of samples for the tests described in the protocol, samples might be used for other resarch by GSK (see protocol). Please tick what is also covered by the subject Informed Consent form of your center.
CL Item
Quality Assurance of tests described in the protocol (This may include the management of the quality of these current tests, the maintenance or (1)
CL Item
improvement of these current tests, the development of new test methods for the markers (improvement of these current tests, the development of new test methods for the markers)
CL Item
described in the protocol as well as making sure that new tests are comparable to previous (described in the protocol as well as making sure that new tests are comparable to previous)
CL Item
methods and work reliably.) (methods and work reliably.))
CL Item
Further investigation by GSK Biologicals into the ability of the vaccine to protect people if (2)
CL Item
any findings from related studies require it and further research in the disease(s) under (any findings from related studies require it and further research in the disease(s) under)
CL Item
study. These investigations excludes genetic and HIV testing. (study. These investigations excludes genetic and HIV testing.)
CL Item
Further research by GSK Biologicals that is NOT RELATED to the vaccine(s) or the disease(s) (3)
CL Item
under study done on an anonymous basis (meaning that any identification linking the subject (under study done on an anonymous basis (meaning that any identification linking the subject)
CL Item
to the sample is destroyed). This research excludes genetic and HIV testing and does not (to the sample is destroyed). This research excludes genetic and HIV testing and does not)
CL Item
affect subject participation in the study. (affect subject participation in the study.)
Item
Please tick below box if a 15 years GSK storage period is covered by the subject’s Informed Consent form of your center.
text
StoragePeriod
Code List
Please tick below box if a 15 years GSK storage period is covered by the subject’s Informed Consent form of your center.
CL Item
At least 15 years storage period by GSK Biologicals (1)
CL Item
Other (2)
Other
Item
If Other, please specify
text
ICF Effective date
Item
ICF Effective date
date
Item Group
Investigator's Signature
Investigator's signature:
Item
Investigator's signature:
text
Date:
Item
Date:
date
Printed Investigator's name:
Item
Printed Investigator's name:
text
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