ID
41509
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
Keywords
Versions (2)
- 9/13/20 9/13/20 -
- 10/30/20 10/30/20 -
Copyright Holder
GlaxoSmithKline
Uploaded on
October 30, 2020
DOI
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License
Creative Commons BY 4.0
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Clinical activity of recMAGE-A3 + AS15 in patients with metastatic cutaneous melanoma NCT00942162
Treatment Conclusion (Report Final and Annex Report 2 Final)
- StudyEvent: ODM
Description
Pregnancy Information
Alias
- UMLS CUI-1
- C0032961
- UMLS CUI-2
- C1533716
Description
Was the patient withdrawn from investigational product or did the patient not attend concluding visit?
Alias
- UMLS CUI-1
- C0422727
- UMLS CUI-2
- C1707478
- UMLS CUI-3
- C0545082
Description
No → Patient has completed Treatment Phase (including Concluding Visit). Please schedule a follow-up visit at Month 60 Yes → Enter reason Patient has been withdrawn from investigational product or did not attend Concluding Visit
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C1707478
- UMLS CUI [1,3]
- C0545082
Description
Patient has been withdrawn from investigational attend Concluding Visit due to:
Data type
text
Alias
- UMLS CUI [1]
- C0422727
- UMLS CUI [2,1]
- C1707478
- UMLS CUI [2,2]
- C0545082
- UMLS CUI [3]
- C0392360
Description
SAE No.
Data type
integer
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0237753
Description
AE No.
Data type
integer
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0237753
Description
Specify protocol violation
Data type
text
Alias
- UMLS CUI [1,1]
- C1709750
- UMLS CUI [1,2]
- C2348235
Description
Other reason Patient has been withdrawn from investigational attend Concluding Visit
Data type
text
Alias
- UMLS CUI [1]
- C0422727
- UMLS CUI [2,1]
- C1707478
- UMLS CUI [2,2]
- C0545082
- UMLS CUI [3]
- C3840932
Description
(tick only one)
Data type
text
Alias
- UMLS CUI [1]
- C0679006
Similar models
Treatment Conclusion (Report Final and Annex Report 2 Final)
- StudyEvent: ODM
C1707478 (UMLS CUI-2)
C0545082 (UMLS CUI-3)
C1707478 (UMLS CUI [1,2])
C0545082 (UMLS CUI [1,3])
C1707478 (UMLS CUI [2,1])
C0545082 (UMLS CUI [2,2])
C0392360 (UMLS CUI [3])
C0237753 (UMLS CUI [1,2])
C0237753 (UMLS CUI [1,2])
C2348235 (UMLS CUI [1,2])
C1707478 (UMLS CUI [2,1])
C0545082 (UMLS CUI [2,2])
C3840932 (UMLS CUI [3])