ID
37214
Description
Study ID: 104864/502 Clinical Study ID: 104864/502 Study Title: An Open-Label, Multicenter, Randomized, Phase II Study of Oral Topotecan Daily x 5 Days vs. Oral Topotecan 5 Days On, 2 Days Off for 3 Weeks for Second-Line Treatment in Patients with Recurrent, Locally Advanced or Metastatic Cervical Cancer Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: N/A Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: Topotecan Trade Name: N/A Study Indication: Cancer, Locally Advanced or Metastatic Cervical Cancer
Keywords
Versions (1)
- 7/8/19 7/8/19 -
Copyright Holder
GlaxoSmithKline
Uploaded on
July 8, 2019
DOI
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License
Creative Commons BY-NC 3.0
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Oral Topotecan Daily x 5 Days vs. Oral Topotacan 5 Days On, 2 Days Off; 104864/502
CRF Tracking/Review Forms
- StudyEvent: ODM
Description
CRF Tracking/Review Form
Alias
- UMLS CUI-1
- C3889409
Description
Clinical Trial Regulatory Tracking Document, Module
Data type
text
Alias
- UMLS CUI [1,1]
- C3889409
- UMLS CUI [1,2]
- C1709061
Description
Clinical Trial Regulatory Tracking Document, Module, Description
Data type
text
Alias
- UMLS CUI [1,1]
- C3889409
- UMLS CUI [1,2]
- C1709061
- UMLS CUI [1,3]
- C0678257
Description
Clinical Trial Regulatory Tracking Document, Page
Data type
text
Alias
- UMLS CUI [1,1]
- C3889409
- UMLS CUI [1,2]
- C1704732
Description
Clinical Trial Regulatory Tracking Document, Module
Data type
text
Alias
- UMLS CUI [1,1]
- C3889409
- UMLS CUI [1,2]
- C1709061
Description
Clinical Trial Regulatory Tracking Document, Page, Missing
Data type
text
Alias
- UMLS CUI [1,1]
- C3889409
- UMLS CUI [1,2]
- C1704732
- UMLS CUI [1,3]
- C1705492
Description
Clinical Trial Regulatory Tracking Document, Comment
Data type
text
Alias
- UMLS CUI [1,1]
- C3889409
- UMLS CUI [1,2]
- C0947611
Description
Clinical Trial Regulatory Tracking Document, Investigator Signature
Data type
text
Alias
- UMLS CUI [1,1]
- C3889409
- UMLS CUI [1,2]
- C2346576
Description
Clinical Trial Regulatory Tracking Document, Submission, Date in time
Data type
date
Alias
- UMLS CUI [1,1]
- C3889409
- UMLS CUI [1,2]
- C1515022
- UMLS CUI [1,3]
- C0011008
Similar models
CRF Tracking/Review Forms
- StudyEvent: ODM
C0600091 (UMLS CUI [1,2])
C1709061 (UMLS CUI [1,2])
C1709061 (UMLS CUI [1,2])
C0678257 (UMLS CUI [1,3])
C1704732 (UMLS CUI [1,2])
C1709061 (UMLS CUI [1,2])
C1704732 (UMLS CUI [1,2])
C1705492 (UMLS CUI [1,3])
C0947611 (UMLS CUI [1,2])
C2346576 (UMLS CUI [1,2])
C1515022 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])