ID
37142
Descripción
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
Palabras clave
Versiones (1)
- 4/7/19 4/7/19 -
Titular de derechos de autor
GlaxoSmithKline
Subido en
4 de julio de 2019
DOI
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Licencia
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
Descripción
Month of Report
Alias
- UMLS CUI-1
- C1704685
- UMLS CUI-2
- C0439231
Descripción
Follow-Up Report, Month
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1704685
- UMLS CUI [1,2]
- C0439231
Descripción
Follow-Up Report, Month
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1704685
- UMLS CUI [1,2]
- C0439231
Descripción
Outcome
Alias
- UMLS CUI-1
- C1547647
Descripción
Cessation of life
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0011065
Descripción
Date last contact
Tipo de datos
date
Alias
- UMLS CUI [1]
- C0805839
Descripción
Disease Progression
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0242656
Descripción
Disease Progression, Start Date
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C0242656
- UMLS CUI [1,2]
- C0808070
Descripción
cancer treatment, post, Clinical Trials
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0920425
- UMLS CUI [1,2]
- C0032756
- UMLS CUI [1,3]
- C0008976
Descripción
cancer treatment, post, Clinical Trials, Start Date
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C0920425
- UMLS CUI [1,2]
- C0032756
- UMLS CUI [1,3]
- C0008976
- UMLS CUI [1,4]
- C0808070
Descripción
Form D
Alias
- UMLS CUI-1
- C0011065
Descripción
Cause of death
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0007465
Descripción
Cause of death
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0007465
Descripción
Date of death
Tipo de datos
date
Alias
- UMLS CUI [1]
- C1148348
Descripción
Autopsy
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0004398
Descripción
Autopsy, Finding, Diagnosis
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0004398
- UMLS CUI [1,2]
- C0243095
- UMLS CUI [1,3]
- C0011900
Descripción
I certify that I have reviewed the follow-up data and that all information is complete and accurate
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0011065
- UMLS CUI [1,2]
- C2346576
Descripción
Cessation of life, Investigator Signature, Date in time
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C0011065
- UMLS CUI [1,2]
- C2346576
- UMLS CUI [1,3]
- C0011008
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- 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])
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C2346576 (UMLS CUI [1,2])
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