ID
41857
Beschrijving
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 the Screening Visit.
Link
https://clinicaltrials.gov/ct2/show/NCT00811733
Trefwoorden
Versies (2)
- 01-02-21 01-02-21 -
- 05-02-21 05-02-21 -
Houder van rechten
GlaxoSmithKline
Geüploaded op
5 februari 2021
DOI
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Licentie
Creative Commons BY-NC 4.0
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GSK Ofatumumab in Waldenstrom Macroglobulinaemia, NCT00811733
Inform Screening
- StudyEvent: ODM
Beschrijving
Inform Screening
Alias
- UMLS CUI-1
- C1552002
- UMLS CUI-2
- C1710032
Beschrijving
[hidden]
Datatype
text
Alias
- UMLS CUI [1]
- C2986440
Beschrijving
Date of Birth
Datatype
date
Alias
- UMLS CUI [1]
- C0421451
Beschrijving
how did you learn about this study?
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0683836
- UMLS CUI [1,2]
- C0012625
- UMLS CUI [1,3]
- C0008976
Beschrijving
primary cause for interest in study
Datatype
text
Alias
- UMLS CUI [1,1]
- C0205225
- UMLS CUI [1,2]
- C0085978
- UMLS CUI [1,3]
- C0008976
- UMLS CUI [1,4]
- C0543488
Beschrijving
source of information, other interned provider
Datatype
text
Alias
- UMLS CUI [1,1]
- C0683836
- UMLS CUI [1,2]
- C0205394
- UMLS CUI [1,3]
- C1138603
Beschrijving
source of information, other
Datatype
text
Alias
- UMLS CUI [1,1]
- C0683836
- UMLS CUI [1,2]
- C0205394
Beschrijving
Trial screen failure
Datatype
boolean
Alias
- UMLS CUI [1]
- C1710476
Beschrijving
check all that apply
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1710476
- UMLS CUI [1,2]
- C1512693
- UMLS CUI [2,1]
- C1710476
- UMLS CUI [2,2]
- C0680251
Beschrijving
Check all that apply
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1710476
- UMLS CUI [1,2]
- C0877248
Beschrijving
Check all that apply
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1710476
- UMLS CUI [1,2]
- C0235828
Beschrijving
Check all that apply
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1710476
- UMLS CUI [1,2]
- C1705236
Beschrijving
Check all that apply
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1710476
- UMLS CUI [1,2]
- C2348563
- UMLS CUI [1,3]
- C2746065
- UMLS CUI [1,4]
- C0243161
Beschrijving
Check all that apply
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1710476
- UMLS CUI [1,2]
- C2348570
Beschrijving
Check all that apply
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1710476
- UMLS CUI [1,2]
- C1302313
Beschrijving
Check all that apply
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1710476
- UMLS CUI [1,2]
- C0008961
- UMLS CUI [1,3]
- C0022423
Beschrijving
investigator discretion specification
Datatype
text
Alias
- UMLS CUI [1,1]
- C0008961
- UMLS CUI [1,2]
- C0022423
- UMLS CUI [1,3]
- C2348235
Beschrijving
Check all that apply
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1710476
- UMLS CUI [1,2]
- C1707492
Beschrijving
Consent withdrawn, specification
Datatype
text
Alias
- UMLS CUI [1,1]
- C1707492
- UMLS CUI [1,2]
- C2348235
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