ID
42085
Description
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 is for logging, if any concomitant medication, (non-)serious adverse events, blood (supportive care) products or additional scans occurred during the study.
Link
https://clinicaltrials.gov/ct2/show/NCT00811733
Keywords
Versions (2)
- 3/30/21 3/30/21 -
- 4/7/21 4/7/21 -
Copyright Holder
GlaxoSmithKline
Uploaded on
March 30, 2021
DOI
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License
Creative Commons BY-NC 4.0
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GSK Ofatumumab in Waldenstrom Macroglobulinaemia, NCT00811733
Log Status
- StudyEvent: ODM
Description
Log Status
Alias
- UMLS CUI-1
- C1708728
- UMLS CUI-2
- C0449438
Description
Concomitant medication taken prior to screening and/or during study
Data type
text
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0332152
- UMLS CUI [1,3]
- C0220908
- UMLS CUI [2,1]
- C2347852
- UMLS CUI [2,2]
- C0347984
- UMLS CUI [2,3]
- C2347804
Description
Non-serious adverse events during study
Data type
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0347984
- UMLS CUI [1,3]
- C2347804
Description
Serious adverse event during study
Data type
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0347984
- UMLS CUI [1,3]
- C2347804
Description
Blood products / blood supportive care products taken during study
Data type
text
Alias
- UMLS CUI [1,1]
- C0456388
- UMLS CUI [1,2]
- C0347984
- UMLS CUI [1,3]
- C2347804
- UMLS CUI [2,1]
- C0018938
- UMLS CUI [2,2]
- C0347984
- UMLS CUI [2,3]
- C2347804
Description
Other/additional scans performed
Data type
text
Alias
- UMLS CUI [1,1]
- C0205394
- UMLS CUI [1,2]
- C0011923
- UMLS CUI [2,1]
- C1524062
- UMLS CUI [2,2]
- C0011923
Similar models
Log Status
- StudyEvent: ODM
C2985720 (UMLS CUI [2])
C0332152 (UMLS CUI [1,2])
C0220908 (UMLS CUI [1,3])
C2347852 (UMLS CUI [2,1])
C0347984 (UMLS CUI [2,2])
C2347804 (UMLS CUI [2,3])
C0347984 (UMLS CUI [1,2])
C2347804 (UMLS CUI [1,3])
C0347984 (UMLS CUI [1,2])
C2347804 (UMLS CUI [1,3])
C0347984 (UMLS CUI [1,2])
C2347804 (UMLS CUI [1,3])
C0018938 (UMLS CUI [2,1])
C0347984 (UMLS CUI [2,2])
C2347804 (UMLS CUI [2,3])
C0011923 (UMLS CUI [1,2])
C1524062 (UMLS CUI [2,1])
C0011923 (UMLS CUI [2,2])
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