ID
41965
Descripción
Study ID: 110921 Clinical Study ID: 110921 Study Title: A Phase II Trial of Ofatumumab in Subjects with Waldenstrom's Macroglobulinemia Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00811733 Clinicaltrials.gov Link: https://clinicaltrials.gov/ct2/show/NCT00811733 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: Ofatumumab Trade Name: N/A Study Indication: Waldenstrom Macroglobulinaemia The primary objective of this open-label, multi-center, Phase II study was to evaluate the safety and efficacy of Ofatumumab in subjects diagnosed with Waldenstrom Macroglobulinaemia. For the study, eligible subjects were enrolled to receive up to 3 cycles of treatment with Ofatumumab. The first cycle consisted of a single dose of 300 mg followed by 3 weekly doses of 1000 mg (Treatment Group A) or 4 weekly doses of 2000 mg (Treatment Group B) of Ofatumumab, with response assessment beginning at Week 12. Based on the Week 12-16 response, eligible subjects could receive up to 2 additional cycles of treatment. This form has to be filled out at any unscheduled visits.
Link
https://clinicaltrials.gov/ct2/show/NCT00811733
Palabras clave
Versiones (2)
- 22/2/21 22/2/21 -
- 24/2/21 24/2/21 -
Titular de derechos de autor
GlaxoSmithKline
Subido en
24 de febrero de 2021
DOI
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Licencia
Creative Commons BY-NC 4.0
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GSK Ofatumumab in Waldenstrom Macroglobulinaemia, NCT00811733
Unscheduled Assessments
- StudyEvent: ODM
Descripción
Unscheduled Assessments
Alias
- UMLS CUI-1
- C0220825
- UMLS CUI-2
- C3854240
Descripción
Select any unscheduled assessments that were performed at this visit.
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0022885
Descripción
Select any unscheduled assessments that were performed at this visit.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0022885
- UMLS CUI [1,2]
- C0205276
Descripción
Select any unscheduled assessments that were performed at this visit.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0005953
- UMLS CUI [1,2]
- C0022885
Descripción
Select any unscheduled assessments that were performed at this visit.
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0009812
Descripción
Select any unscheduled assessments that were performed at this visit.
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C1520224
Descripción
Select any unscheduled assessments that were performed at this visit.
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0518766
Descripción
Select any unscheduled assessments that were performed at this visit.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0031809
- UMLS CUI [1,2]
- C0178784
Descripción
Select any unscheduled assessments that were performed at this visit.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0031809
- UMLS CUI [1,2]
- C0024204
Descripción
Select any unscheduled assessments that were performed at this visit.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0521982
- UMLS CUI [1,2]
- C0220825
Descripción
Select any unscheduled assessments that were performed at this visit.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0040405
- UMLS CUI [1,2]
- C0178784
- UMLS CUI [2,1]
- C0040405
- UMLS CUI [2,2]
- C0024204
Similar models
Unscheduled Assessments
- StudyEvent: ODM
C2985720 (UMLS CUI [2])
C3854240 (UMLS CUI-2)
C0205276 (UMLS CUI [1,2])
C0022885 (UMLS CUI [1,2])
C0178784 (UMLS CUI [1,2])
C0024204 (UMLS CUI [1,2])
C0220825 (UMLS CUI [1,2])
C0178784 (UMLS CUI [1,2])
C0040405 (UMLS CUI [2,1])
C0024204 (UMLS CUI [2,2])
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