ID
37142
Beschrijving
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
Trefwoorden
Versies (1)
- 04-07-19 04-07-19 -
Houder van rechten
GlaxoSmithKline
Geüploaded op
4 juli 2019
DOI
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Licentie
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
Post-Study Minimal Follow-Up Report
- StudyEvent: ODM
Beschrijving
Month of Report
Alias
- UMLS CUI-1
- C1704685
- UMLS CUI-2
- C0439231
Beschrijving
Follow-Up Report, Month
Datatype
text
Alias
- UMLS CUI [1,1]
- C1704685
- UMLS CUI [1,2]
- C0439231
Beschrijving
Follow-Up Report, Month
Datatype
text
Alias
- UMLS CUI [1,1]
- C1704685
- UMLS CUI [1,2]
- C0439231
Beschrijving
Outcome
Alias
- UMLS CUI-1
- C1547647
Beschrijving
Cessation of life
Datatype
boolean
Alias
- UMLS CUI [1]
- C0011065
Beschrijving
Date last contact
Datatype
date
Alias
- UMLS CUI [1]
- C0805839
Beschrijving
Disease Progression
Datatype
text
Alias
- UMLS CUI [1]
- C0242656
Beschrijving
Disease Progression, Start Date
Datatype
date
Alias
- UMLS CUI [1,1]
- C0242656
- UMLS CUI [1,2]
- C0808070
Beschrijving
cancer treatment, post, Clinical Trials
Datatype
text
Alias
- UMLS CUI [1,1]
- C0920425
- UMLS CUI [1,2]
- C0032756
- UMLS CUI [1,3]
- C0008976
Beschrijving
cancer treatment, post, Clinical Trials, Start Date
Datatype
date
Alias
- UMLS CUI [1,1]
- C0920425
- UMLS CUI [1,2]
- C0032756
- UMLS CUI [1,3]
- C0008976
- UMLS CUI [1,4]
- C0808070
Beschrijving
Form D
Alias
- UMLS CUI-1
- C0011065
Beschrijving
Cause of death
Datatype
text
Alias
- UMLS CUI [1]
- C0007465
Beschrijving
Cause of death
Datatype
text
Alias
- UMLS CUI [1]
- C0007465
Beschrijving
Date of death
Datatype
date
Alias
- UMLS CUI [1]
- C1148348
Beschrijving
Autopsy
Datatype
boolean
Alias
- UMLS CUI [1]
- C0004398
Beschrijving
Autopsy, Finding, Diagnosis
Datatype
text
Alias
- UMLS CUI [1,1]
- C0004398
- UMLS CUI [1,2]
- C0243095
- UMLS CUI [1,3]
- C0011900
Beschrijving
I certify that I have reviewed the follow-up data and that all information is complete and accurate
Datatype
text
Alias
- UMLS CUI [1,1]
- C0011065
- UMLS CUI [1,2]
- C2346576
Beschrijving
Cessation of life, Investigator Signature, Date in time
Datatype
date
Alias
- UMLS CUI [1,1]
- C0011065
- UMLS CUI [1,2]
- C2346576
- UMLS CUI [1,3]
- C0011008
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Post-Study Minimal Follow-Up Report
- StudyEvent: ODM
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C0808070 (UMLS CUI [1,2])
C0032756 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
C0032756 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
C0808070 (UMLS CUI [1,4])
C0243095 (UMLS CUI [1,2])
C0011900 (UMLS CUI [1,3])
C2346576 (UMLS CUI [1,2])
C2346576 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])