ID

41378

Description

Study ID: 111476 Clinical Study ID: 111476 Study Title: An open, single-arm trial to assess the clinical activity of recMAGE-A3 + AS15 in patients with unresectable MAGE-A3-positive metastatic cutaneous melanoma Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00942162 Sponsor: GlaxoSmithKline Phase: Phase 2 Study Recruitment Status: Completed Generic Name: Antigen-Specific Cancer Immunotherapeutic Study Indication: Melanoma

Mots-clés

  1. 17/09/2020 17/09/2020 -
  2. 30/10/2020 30/10/2020 -
Détendeur de droits

GlaxoSmithKline

Téléchargé le

17 septembre 2020

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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Clinical activity of recMAGE-A3 + AS15 in patients with metastatic cutaneous melanoma NCT00942162

One Year Survival Assessment

Administrative
Description

Administrative

Alias
UMLS CUI-1
C1320722
Patient Number
Description

Patient Number

Type de données

text

Alias
UMLS CUI [1]
C2348585
One Year Survival Assessment
Description

One Year Survival Assessment

Alias
UMLS CUI-1
C0220921
UMLS CUI-2
C0220825
Did the patient return for the One year survival assessment from time of registration?
Description

Did the patient return for the One year survival assessment from time of registration?

Type de données

boolean

Alias
UMLS CUI [1,1]
C0220921
UMLS CUI [1,2]
C0220825
UMLS CUI [2]
C0332156
UMLS CUI [3]
C1514821
Date of visit:
Description

Date of visit:

Type de données

date

Alias
UMLS CUI [1]
C1320303
If the patient did not return for the One year survival assessment from time of registration, is the patient still alive?
Description

If the patient did not return for the One year survival assessment from time of registration, is the patient still alive?

Type de données

text

Alias
UMLS CUI [1,1]
C0220921
UMLS CUI [1,2]
C0220825
UMLS CUI [2]
C0332156
UMLS CUI [3]
C1514821
UMLS CUI [4]
C2584946
If the patient is still alive, enter date of contact
Description

If the patient is still alive, enter date of contact

Type de données

date

Alias
UMLS CUI [1]
C2584946
UMLS CUI [2,1]
C0011008
UMLS CUI [2,2]
C1705415
If unkown if patient is still alive, specify the reason
Description

If unkown if patient is still alive, specify the reason

Type de données

text

Alias
UMLS CUI [1]
C2584946
UMLS CUI [2,1]
C0392360
UMLS CUI [2,2]
C2348235
Other reason for unkown if patient is still alive
Description

Other reason for unkown if patient is still alive

Type de données

text

Alias
UMLS CUI [1]
C2584946
UMLS CUI [2]
C3840932

Similar models

One Year Survival Assessment

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Administrative
C1320722 (UMLS CUI-1)
Patient Number
Item
Patient Number
text
C2348585 (UMLS CUI [1])
Item Group
One Year Survival Assessment
C0220921 (UMLS CUI-1)
C0220825 (UMLS CUI-2)
Did the patient return for the One year survival assessment from time of registration?
Item
Did the patient return for the One year survival assessment from time of registration?
boolean
C0220921 (UMLS CUI [1,1])
C0220825 (UMLS CUI [1,2])
C0332156 (UMLS CUI [2])
C1514821 (UMLS CUI [3])
Date of visit:
Item
Date of visit:
date
C1320303 (UMLS CUI [1])
Item
If the patient did not return for the One year survival assessment from time of registration, is the patient still alive?
text
C0220921 (UMLS CUI [1,1])
C0220825 (UMLS CUI [1,2])
C0332156 (UMLS CUI [2])
C1514821 (UMLS CUI [3])
C2584946 (UMLS CUI [4])
Code List
If the patient did not return for the One year survival assessment from time of registration, is the patient still alive?
CL Item
Yes (Y)
CL Item
No (N)
CL Item
Unknown (U)
If the patient is still alive, enter date of contact
Item
If the patient is still alive, enter date of contact
date
C2584946 (UMLS CUI [1])
C0011008 (UMLS CUI [2,1])
C1705415 (UMLS CUI [2,2])
Item
If unkown if patient is still alive, specify the reason
text
C2584946 (UMLS CUI [1])
C0392360 (UMLS CUI [2,1])
C2348235 (UMLS CUI [2,2])
Code List
If unkown if patient is still alive, specify the reason
CL Item
Lost to follow-up (LFU)
CL Item
Consent withdrawal (CWS)
CL Item
Other, specify (OTH)
Other reason for unkown if patient is still alive
Item
Other reason for unkown if patient is still alive
text
C2584946 (UMLS CUI [1])
C3840932 (UMLS CUI [2])

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