ID

36175

Beschrijving

Study ID: 109616 (Y7), 109624 Clinical Study ID: 109616 (Y7) Study Title: A blinded long-term follow-up study of the efficacy of candidate HPV-16/18 L1 VLP AS04 vaccine in young adult women in Brazil vaccinated in the phase IIb, double-blind, multi- center primary study HPV-001 and having participated in the follow-up study HPV-007 Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00518336 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: HPV Vaccine Trade Name: Cervarix Study Indication: Infections, Papillomavirus

Trefwoorden

Versies (1)
  1. 22-04-19 22-04-19 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

22 april 2019

DOI

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Licentie

Creative Commons BY-NC 3.0
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Candidate HPV-16/18 L1 VLP A04 Vaccine in Young Adult Women Vaccinated in Phase IIb, NCT00518336

Engels

Concomitant Vaccination

1 Formulieren  
Administrative Data
Beschrijving

Administrative Data

Alias
UMLS CUI-1
C1320722
Subject Number
Beschrijving

Clinical Trial Subject Unique Identifier

Datatype

integer

Alias
UMLS CUI [1]
C2348585
Concomitant Vaccination
Beschrijving

Concomitant Vaccination

Alias
UMLS CUI-1
C0042196
UMLS CUI-2
C2347852
Have any HPV vaccine other than that used in the study HPV-001 or any investigational vaccine been administered at any time during the study?
Beschrijving

Human Papilloma Virus Vaccine, Other

Datatype

boolean

Alias
UMLS CUI [1,1]
C1512511
UMLS CUI [1,2]
C0205394
Trade / (Generic) Name
Beschrijving

Vaccination, Concomitant Agent, Medication Name

Datatype

text

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

Vaccination, Concomitant Agent, Drug Administration Routes

Datatype

text

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

Vaccination, Concomitant Agent, Date in time

Datatype

date

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

Concomitant Vaccination

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
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
C0042196 (UMLS CUI-1)
C2347852 (UMLS CUI-2)
Human Papilloma Virus Vaccine, Other
Item
Have any HPV vaccine other than that used in the study HPV-001 or any investigational vaccine been administered at any time during the study?
boolean
C1512511 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
Vaccination, Concomitant Agent, Medication Name
Item
Trade / (Generic) Name
text
C0042196 (UMLS CUI [1,1])
C2347852 (UMLS CUI [1,2])
C2360065 (UMLS CUI [1,3])
Vaccination, Concomitant Agent, Drug Administration Routes
Item
Route
text
C0042196 (UMLS CUI [1,1])
C2347852 (UMLS CUI [1,2])
C0013153 (UMLS CUI [1,3])
Vaccination, Concomitant Agent, Date in time
Item
Administration date
date
C0042196 (UMLS CUI [1,1])
C2347852 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
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