ID

41672

Description

Study ID: 105874 Clinical Study ID: 105874 Study Title: Bridging Safety & Immunogenicity Study of GSK Biologicals' Candidate Malaria Vaccine RTS,S/AS01E (0.5 mL Dose) to RTS,S/AS02D (0.5 mL Dose) Administered IM According to a 0, 1, 2-Month Schedule in Gabonese Children Aged 18 Months to 4 Years Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00307021 https://clinicaltrials.gov/ct2/show/NCT00307021 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: GSK Biologicals' candidate Plasmodium falciparum malaria vaccine 257049 Trade Name: N/A Study Indication: Malaria This study has a total of 7 visits. Visit 1 = Screening, Visits 2-6 are during the double-blind phase (Month 0-3) and Visit 7 is during the single-blind phase (Month 4-14). This form (Contraindications to subsequent vaccination) should be filled out whenever a vaccination is due. Indications for deferral of vaccination: The following AEs constitute contraindications to administration of RTS,S/AS02D or RTS,S/AS01E at that point in time; if any one of these AEs occur at the time scheduled for vaccination, the subject may be vaccinated at a later date, within the time window specified in the protocol, or withdrawn at the discretion of the investigator. Absolute contraindications to further vaccination: The following AEs constitute absolute contraindications to further administration of RTS,S/AS02D or RTS,S/AS01E; if any of these AEs occur during the study, the subject must not receive additional doses of vaccine, but may continue other study procedures at the discretion of the investigator.

Lien

https://clinicaltrials.gov/ct2/show/NCT00307021

Mots-clés

  1. 09/12/2020 09/12/2020 -
Détendeur de droits

GlaxoSmithKline

Téléchargé le

9 décembre 2020

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 4.0

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Safety & Immunogenicity of two GSK Biologicals' Candidate Malaria Vaccines in young children, NCT00307021

Contraindications to subsequent vaccination

Administrative Data
Description

Administrative Data

Alias
UMLS CUI-1
C1320722
Subject number
Description

Subject number

Type de données

text

Alias
UMLS CUI [1]
C2348585
Date of visit/assessment
Description

Date of visit/assessment

Type de données

date

Alias
UMLS CUI [1]
C1320303
UMLS CUI [2]
C2985720
Indications for deferral of vaccination
Description

Indications for deferral of vaccination

Alias
UMLS CUI-1
C0205421
UMLS CUI-2
C0042196
UMLS CUI-3
C3146298
[A] Acute disease at the time of administration of investigational product (acute disease is defined as the presence of a moderate or severe illness with or without fever). All vaccines can be administered to persons with a minor illness such as diarrhea or mild upper respiratory infection without fever, i.e. axillary temperature < 37.5°C.
Description

Acute disease at the time of administration of investigational product

Type de données

boolean

Alias
UMLS CUI [1,1]
C0001314
UMLS CUI [1,2]
C0150312
UMLS CUI [1,3]
C2368628
[B] Axillary temperature of >= 37.5°C.
Description

Axillary temperature

Type de données

boolean

Alias
UMLS CUI [1]
C1531924
Absolute contraindications to further vaccination
Description

Absolute contraindications to further vaccination

Alias
UMLS CUI-1
C0522473
UMLS CUI-2
C0042196
[C] Acute allergic reaction (significant IgE-mediated events) or anaphylaxis following the administration of vaccine investigational product.
Description

Acute allergic reaction or anaphylaxis following administration of vaccine

Type de données

boolean

Alias
UMLS CUI [1,1]
C0042196
UMLS CUI [1,2]
C0020517
UMLS CUI [2,1]
C0002792
UMLS CUI [2,2]
C0042196
[D] Any confirmed or suspected immunosuppressive or immunodeficient condition, including human immunodeficiency virus (HIV) infection.
Description

Immunosuppressive or immunodeficient condition, including HIV

Type de données

boolean

Alias
UMLS CUI [1]
C4048329
UMLS CUI [2]
C0021051
UMLS CUI [3]
C0019693
[E] Failure to thrive.
Description

Failure to thrive

Type de données

boolean

Alias
UMLS CUI [1]
C0015544

Similar models

Contraindications to subsequent vaccination

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Administrative Data
C1320722 (UMLS CUI-1)
Subject number
Item
Subject number
text
C2348585 (UMLS CUI [1])
Date of visit/assessment
Item
Date of visit/assessment
date
C1320303 (UMLS CUI [1])
C2985720 (UMLS CUI [2])
Item Group
Indications for deferral of vaccination
C0205421 (UMLS CUI-1)
C0042196 (UMLS CUI-2)
C3146298 (UMLS CUI-3)
Acute disease at the time of administration of investigational product
Item
[A] Acute disease at the time of administration of investigational product (acute disease is defined as the presence of a moderate or severe illness with or without fever). All vaccines can be administered to persons with a minor illness such as diarrhea or mild upper respiratory infection without fever, i.e. axillary temperature < 37.5°C.
boolean
C0001314 (UMLS CUI [1,1])
C0150312 (UMLS CUI [1,2])
C2368628 (UMLS CUI [1,3])
Axillary temperature
Item
[B] Axillary temperature of >= 37.5°C.
boolean
C1531924 (UMLS CUI [1])
Item Group
Absolute contraindications to further vaccination
C0522473 (UMLS CUI-1)
C0042196 (UMLS CUI-2)
Acute allergic reaction or anaphylaxis following administration of vaccine
Item
[C] Acute allergic reaction (significant IgE-mediated events) or anaphylaxis following the administration of vaccine investigational product.
boolean
C0042196 (UMLS CUI [1,1])
C0020517 (UMLS CUI [1,2])
C0002792 (UMLS CUI [2,1])
C0042196 (UMLS CUI [2,2])
Immunosuppressive or immunodeficient condition, including HIV
Item
[D] Any confirmed or suspected immunosuppressive or immunodeficient condition, including human immunodeficiency virus (HIV) infection.
boolean
C4048329 (UMLS CUI [1])
C0021051 (UMLS CUI [2])
C0019693 (UMLS CUI [3])
Failure to thrive
Item
[E] Failure to thrive.
boolean
C0015544 (UMLS CUI [1])

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