ID

41866

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 has to be filled out at the Screening Visit.

Link

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

Palabras clave

  1. 8/2/21 8/2/21 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

8 de febrero de 2021

DOI

Para solicitar uno, por favor iniciar sesión.

Licencia

Creative Commons BY-NC 4.0

Comentarios del modelo :

Puede comentar sobre el modelo de datos aquí. A través de las burbujas de diálogo en los grupos de elementos y elementos, puede agregar comentarios específicos.

Comentarios de grupo de elementos para :

Comentarios del elemento para :


Sin comentarios

Para descargar modelos de datos, debe haber iniciado sesión. Por favor iniciar sesión o Registrate gratis.

GSK Ofatumumab in Waldenstrom Macroglobulinaemia, NCT00811733

Medical History

  1. StudyEvent: ODM
    1. Medical History
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
Status Questions
Descripción

Status Questions

Alias
UMLS CUI-1
C0449437
Does the subject have any current or previous Medical Conditions?
Descripción

Medical History

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0262926
Medical Conditions
Descripción

Medical Conditions

Alias
UMLS CUI-1
C0012634
Sequence number
Descripción

[hidden]

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C2348184
Specific condition
Descripción

Specific condition

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C2348235
Modified term
Descripción

[hidden]

Tipo de datos

text

Alias
UMLS CUI [1]
C2826923
MedDRA Synonym
Descripción

[hidden]

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C1140263
MedDRA lower level term code
Descripción

[hidden]

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C3898442
failed coding
Descripción

[hidden]

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C0805701
UMLS CUI [1,3]
C0231175
NCI CTCAE v.3 Grade
Descripción

Disease, NCI CTCAE v.3 Grade

Tipo de datos

text

Alias
UMLS CUI [1]
C3887242
Status
Descripción

Disease status

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C0449438
Classification
Descripción

Disease classification

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C0008902

Similar models

Medical History

  1. StudyEvent: ODM
    1. Medical History
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 Group
Status Questions
C0449437 (UMLS CUI-1)
Medical History
Item
Does the subject have any current or previous Medical Conditions?
boolean
C0262926 (UMLS CUI [1])
Item Group
Medical Conditions
C0012634 (UMLS CUI-1)
Disease sequence number
Item
Sequence number
text
C0012634 (UMLS CUI [1,1])
C2348184 (UMLS CUI [1,2])
Specific condition
Item
Specific condition
text
C0012634 (UMLS CUI [1,1])
C2348235 (UMLS CUI [1,2])
Disease, modified term
Item
Modified term
text
C2826923 (UMLS CUI [1])
Disease, MedDRA Synonym
Item
MedDRA Synonym
text
C0012634 (UMLS CUI [1,1])
C1140263 (UMLS CUI [1,2])
Disease, MedDRA lower level term code
Item
MedDRA lower level term code
text
C0012634 (UMLS CUI [1,1])
C3898442 (UMLS CUI [1,2])
Disease, failed coding
Item
failed coding
text
C0012634 (UMLS CUI [1,1])
C0805701 (UMLS CUI [1,2])
C0231175 (UMLS CUI [1,3])
Item
NCI CTCAE v.3 Grade
text
C3887242 (UMLS CUI [1])
Code List
NCI CTCAE v.3 Grade
CL Item
Grade 1  (1)
CL Item
Grade 2 (2)
CL Item
Grade 3 (3)
CL Item
Grade 4 (4)
CL Item
Not Applicable (X)
Item
Status
integer
C0012634 (UMLS CUI [1,1])
C0449438 (UMLS CUI [1,2])
Code List
Status
CL Item
current (1)
CL Item
past (2)
Item
Classification
text
C0012634 (UMLS CUI [1,1])
C0008902 (UMLS CUI [1,2])
Code List
Classification
CL Item
Cancer related (24)
CL Item
Toxicities relate to previous therapy  (29)
CL Item
Other (general) (OT)

Utilice este formulario para comentarios, preguntas y sugerencias.

Los campos marcados con * son obligatorios.

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