ID

44788

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 is for documentation of electronically transferred lab data and is used for screening, cycle 1 weeks 1-4 and observation, cycle 2 weeks 1-4 and observation and on a potential withdrawal visit, as well as any unscheduled lab data available.

Link

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

Palabras clave

  1. 26/11/21 26/11/21 - Sarah Riepenhausen
Titular de derechos de autor

GlaxoSmithKline

Subido en

26 de noviembre de 2021

DOI

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Licencia

Creative Commons BY-NC 4.0

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GSK Ofatumumab in Waldenstrom Macroglobulinaemia, NCT00811733

Electronically transferred lab data

Administrative Data
Descripción

Administrative Data

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

date of visit/assessment

Tipo de datos

date

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

subject ID

Tipo de datos

text

Alias
UMLS CUI [1]
C2348585
visit type
Descripción

visit type

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0545082
UMLS CUI [1,2]
C0332307
Electronically transferred lab data- blood sample
Descripción

Electronically transferred lab data- blood sample

Alias
UMLS CUI [1]
C0005834
Date sample taken
Descripción

Blood sample taken

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0005834
UMLS CUI [1,2]
C0884358
Date
Descripción

[read-only]

Tipo de datos

date

Alias
UMLS CUI [1,1]
C0005834
UMLS CUI [1,2]
C0011008
Electronically transferred lab data - Neuro AB Panel
Descripción

Electronically transferred lab data - Neuro AB Panel

Alias
UMLS CUI [1,1]
C0027763
UMLS CUI [1,2]
C0003241
UMLS CUI [1,3]
C0370003
Date sample taken
Descripción

Neuro Antibody panel sample taken

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0027763
UMLS CUI [1,2]
C0003241
UMLS CUI [1,3]
C0370003
UMLS CUI [1,4]
C0884358
Date
Descripción

Date neuro antibody panel sample taken

Tipo de datos

date

Alias
UMLS CUI [1,1]
C0027763
UMLS CUI [1,2]
C0003241
UMLS CUI [1,3]
C0370003
UMLS CUI [1,4]
C0011008
Electronically transferred lab data - prognostic factors
Descripción

Electronically transferred lab data - prognostic factors

Alias
UMLS CUI [1,1]
C1514474
UMLS CUI [1,2]
C0370003
Date sample taken
Descripción

Prognostic factor sample taken

Tipo de datos

text

Alias
UMLS CUI [1,1]
C1514474
UMLS CUI [1,2]
C0370003
UMLS CUI [1,3]
C0884358
Date
Descripción

Date prognostic factor sample

Tipo de datos

date

Alias
UMLS CUI [1,1]
C1514474
UMLS CUI [1,2]
C0370003
UMLS CUI [1,3]
C0011008

Similar models

Electronically transferred lab data

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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
visit type
text
C0545082 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
Code List
visit type
CL Item
Cycle 1 week 1 (1)
CL Item
Cycle 1 week 2 (2)
CL Item
Cycle 1 week 3 (3)
CL Item
Cycle 1 week 4 (4)
CL Item
Cycle 1 Observation visit (5)
CL Item
Cycle 2 week 1 (6)
CL Item
Cycle 2 week 2 (7)
CL Item
Cycle 2 week 3 (8)
CL Item
Cycle 2 week 4 (9)
(Comment:en)
CL Item
Cycle 2 observation visit (10)
(Comment:en)
CL Item
Withdrawal Visit (11)
(Comment:en)
CL Item
Screening (0)
(Comment:en)
CL Item
Unscheduled visit (12)
(Comment:en)
Item Group
Electronically transferred lab data- blood sample
C0005834 (UMLS CUI [1])
Item
Date sample taken
text
C0005834 (UMLS CUI [1,1])
C0884358 (UMLS CUI [1,2])
Code List
Date sample taken
CL Item
Date available (99)
CL Item
Not Done (ND)
Date blood sample taken
Item
Date
date
C0005834 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item Group
Electronically transferred lab data - Neuro AB Panel
C0027763 (UMLS CUI [1,1])
C0003241 (UMLS CUI [1,2])
C0370003 (UMLS CUI [1,3])
Item
Date sample taken
text
C0027763 (UMLS CUI [1,1])
C0003241 (UMLS CUI [1,2])
C0370003 (UMLS CUI [1,3])
C0884358 (UMLS CUI [1,4])
Code List
Date sample taken
CL Item
Date available (99)
CL Item
Not done (ND)
Date neuro antibody panel sample taken
Item
Date
date
C0027763 (UMLS CUI [1,1])
C0003241 (UMLS CUI [1,2])
C0370003 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,4])
Item Group
Electronically transferred lab data - prognostic factors
C1514474 (UMLS CUI [1,1])
C0370003 (UMLS CUI [1,2])
Item
Date sample taken
text
C1514474 (UMLS CUI [1,1])
C0370003 (UMLS CUI [1,2])
C0884358 (UMLS CUI [1,3])
Code List
Date sample taken
CL Item
Date available (99)
CL Item
Not done (ND)
Date prognostic factor sample
Item
Date
date
C1514474 (UMLS CUI [1,1])
C0370003 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])

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