ID

41958

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 observation visit of the first treatment cycle.

Link

https://clinicaltrials.gov/ct2/show/NCT00811733

Trefwoorden

  1. 22-02-21 22-02-21 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

22 februari 2021

DOI

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Licentie

Creative Commons BY-NC 4.0

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GSK Ofatumumab in Waldenstrom Macroglobulinaemia, NCT00811733

Retreatment Question

  1. StudyEvent: ODM
    1. Retreatment Question
Administrative Data
Beschrijving

Administrative Data

Alias
UMLS CUI-1
C1320722
date of visit/assessment
Beschrijving

date of visit/assessment

Datatype

date

Alias
UMLS CUI [1]
C1320303
UMLS CUI [2]
C2985720
subject number
Beschrijving

subject ID

Datatype

text

Alias
UMLS CUI [1]
C2348585
Retreatment Question
Beschrijving

Retreatment Question

Alias
UMLS CUI-1
C0376495
Has a second cycle of study drug been scheduled?
Beschrijving

Retreatment status

Datatype

boolean

Alias
UMLS CUI [1,1]
C0376495
UMLS CUI [1,2]
C0449438

Similar models

Retreatment Question

  1. StudyEvent: ODM
    1. Retreatment Question
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Administrative Data
C1320722 (UMLS CUI-1)
date of visit/assessment
Item
date of visit/assessment
date
C1320303 (UMLS CUI [1])
C2985720 (UMLS CUI [2])
subject ID
Item
subject number
text
C2348585 (UMLS CUI [1])
Item Group
Retreatment Question
C0376495 (UMLS CUI-1)
Retreatment status
Item
Has a second cycle of study drug been scheduled?
boolean
C0376495 (UMLS CUI [1,1])
C0449438 (UMLS CUI [1,2])

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