ID

41889

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 has to be filled out at the screening visit, the weekly visits during the cycles of treatment, the cycle observation visits, unscheduled visits, withdrawal visits and visits at the end of study/ treatment.

Link

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

Keywords

  1. 2/9/21 2/9/21 -
Copyright Holder

GlaxoSmithKline

Uploaded on

February 9, 2021

DOI

To request one please log in.

License

Creative Commons BY-NC 4.0

Model comments :

You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.

Itemgroup comments for :

Item comments for :


No comments

In order to download data models you must be logged in. Please log in or register for free.

GSK Ofatumumab in Waldenstrom Macroglobulinaemia, NCT00811733

Constitutional Symptoms and ECOG

Administrative Data
Description

Administrative Data

Alias
UMLS CUI-1
C1320722 (Administrative documentation)
SNOMED
405624007
date of visit/assessment
Description

date of visit/assessment

Data type

date

Alias
UMLS CUI [1]
C1320303 (Date of visit)
SNOMED
406543005
UMLS CUI [2]
C2985720 (Assessment Date)
subject number
Description

subject ID

Data type

text

Alias
UMLS CUI [1]
C2348585 (Clinical Trial Subject Unique Identifier)
visit type
Description

visit type

Data type

text

Alias
UMLS CUI [1,1]
C0545082 (Visit)
UMLS CUI [1,2]
C0332307 (Type - attribute)
SNOMED
261664005
Constitutional Symptoms
Description

Constitutional Symptoms

Alias
UMLS CUI-1
C0009812 (Constitutional Symptom)
Night sweats without signs of infection
Description

Night sweats without signs of infection

Data type

boolean

Alias
UMLS CUI [1,1]
C0028081 (Night sweats)
SNOMED
42984000
LOINC
LP75171-6
UMLS CUI [1,2]
C0009450 (Communicable Diseases)
SNOMED
189822004
UMLS CUI [1,3]
C0332197 (Absent)
SNOMED
2667000
LOINC
LA9634-2
Unintentional weight loss >= 10% within the previous 6 months
Description

Recent unintentional weight loss

Data type

boolean

Alias
UMLS CUI [1,1]
C0332185 (Recent)
SNOMED
6493001
UMLS CUI [1,2]
C2363736 (Unintentional weight loss)
SNOMED
448765001
Recurrent, unexplained fever of greater than 100°F for 2 weeks without signs of infection
Description

Recurrent, unexplained fever

Data type

boolean

Alias
UMLS CUI [1,1]
C2945760 (Recurrent)
SNOMED
255227004
UMLS CUI [1,2]
C1844662 (Unexplained fevers)
Extreme fatigue
Description

Extreme fatigue

Data type

boolean

Alias
UMLS CUI [1,1]
C0205403 (Extreme)
SNOMED
12565001
LOINC
LA14868-6
UMLS CUI [1,2]
C0015672 (Fatigue)
SNOMED
248274002
LOINC
MTHU013358
ECOG Performance Status Scale
Description

ECOG Performance Status Scale

Alias
UMLS CUI-1
C1520224 (ECOG performance status)
SNOMED
423740007
Total Score
Description

ECOG Performance status, total score

Data type

text

Alias
UMLS CUI [1,1]
C1520224 (ECOG performance status)
SNOMED
423740007
UMLS CUI [1,2]
C2964552 (Total score)
LOINC
LP101867-2

Similar models

Constitutional Symptoms and ECOG

Name
Type
Description | Question | Decode (Coded Value)
Data type
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
Screening visit (A)
CL Item
Cycle 1 week 1 (B)
CL Item
Cycle 1 week 2 (C)
CL Item
Cycle 1 week 3  (D)
CL Item
Cycle 1 week 4 (E)
CL Item
Cycle 1 Observation  (F)
CL Item
unscheduled visit (G)
CL Item
Withdrawal visit (H)
CL Item
End of Study / Treatment (I)
CL Item
Cycle 2 Week 1 (J)
CL Item
Cycle 2 Week 2 (K)
CL Item
Cycle 2 Week 3 (L)
CL Item
Cycle 2 Week 4 (M)
CL Item
Cycle 2 Observation (N)
Item Group
Constitutional Symptoms
C0009812 (UMLS CUI-1)
Night sweats without signs of infection
Item
Night sweats without signs of infection
boolean
C0028081 (UMLS CUI [1,1])
C0009450 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
Recent unintentional weight loss
Item
Unintentional weight loss >= 10% within the previous 6 months
boolean
C0332185 (UMLS CUI [1,1])
C2363736 (UMLS CUI [1,2])
Recurrent, unexplained fever
Item
Recurrent, unexplained fever of greater than 100°F for 2 weeks without signs of infection
boolean
C2945760 (UMLS CUI [1,1])
C1844662 (UMLS CUI [1,2])
Extreme fatigue
Item
Extreme fatigue
boolean
C0205403 (UMLS CUI [1,1])
C0015672 (UMLS CUI [1,2])
Item Group
ECOG Performance Status Scale
C1520224 (UMLS CUI-1)
ECOG Performance status, total score
Item
Total Score
text
C1520224 (UMLS CUI [1,1])
C2964552 (UMLS CUI [1,2])

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial