ID

31385

Beschrijving

Study ID: 104507 Clinical Study ID: BEX104507 Study Title: Phase II Study of Iodine-131 Anti-B1 Antibody for Non Hodgkin’s Lymphoma Patients who have Previously Received Rituximab Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00996593 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: tositumomab Trade Name: Bexxar Study Indication: Lymphoma, Non-Hodgkin

Trefwoorden

Versies (2)
  1. 06-08-18 06-08-18 -
  2. 18-08-18 18-08-18 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

18 augustus 2018

DOI

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Creative Commons BY-NC 3.0
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Iodine-131 Anti-B1 Antibody for Non Hodgkin’s Lymphomas NCT00996593

Engels

Independent Response Evaluation Oncologist's Assessment and Consensus Criteria

1 Formulieren  
Response
Beschrijving

Response

Alias
UMLS CUI-1
C0521982
Date of Response
Beschrijving

Date of Response

Datatype

date

Alias
UMLS CUI [1,1]
C0521982
UMLS CUI [1,2]
C0011008
Response
Beschrijving

Response

Datatype

text

Alias
UMLS CUI [1]
C0521982
Comments
Beschrijving

Comments

Datatype

text

Alias
UMLS CUI [1]
C0947611
Consensus Criteria
Beschrijving

Consensus Criteria

Alias
UMLS CUI-1
C0376298
UMLS CUI-2
C0243161
Response Date (mm/dd/yyyy)
Beschrijving

Response to treatment; Date in time

Datatype

date

Alias
UMLS CUI [1,1]
C0521982
UMLS CUI [1,2]
C0011008
Consensus Response
Beschrijving

Consensus; Response to treatment

Datatype

text

Alias
UMLS CUI [1,1]
C0376298
UMLS CUI [1,2]
C0521982
Comments
Beschrijving

Comments

Datatype

text

Alias
UMLS CUI [1]
C0947611
Administrative
Beschrijving

Administrative

Alias
UMLS CUI-1
C1320722
Oncologist's Signature
Beschrijving

oncologist; Signature

Datatype

text

Alias
UMLS CUI [1,1]
C0259990
UMLS CUI [1,2]
C1519316
Date of evaluation
Beschrijving

Assessment Date

Datatype

date

Alias
UMLS CUI [1]
C2985720
Terug naar het begin van de pagina

Similar models

Independent Response Evaluation Oncologist's Assessment and Consensus Criteria

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Response
C0521982 (UMLS CUI-1)
Date of Response
Item
Date of Response
date
C0521982 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item
Response
text
C0521982 (UMLS CUI [1])
Response
Code List
Response
CL Item
CR (5)
CL Item
CCR (4)
CL Item
PR (3)
CL Item
SD (2)
CL Item
PD (1)
CL Item
NA / (baseline) (N)
Comments
Item
Comments
text
C0947611 (UMLS CUI [1])
Item Group
Consensus Criteria
C0376298 (UMLS CUI-1)
C0243161 (UMLS CUI-2)
Response to treatment; Date in time
Item
Response Date (mm/dd/yyyy)
date
C0521982 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item
Consensus Response
text
C0376298 (UMLS CUI [1,1])
C0521982 (UMLS CUI [1,2])
Consensus; Response to treatment
Code List
Consensus Response
CL Item
CR (5)
CL Item
CRu (4)
CL Item
PR (3)
CL Item
SD (2)
CL Item
PD (1)
CL Item
NA (N)
Comments
Item
Comments
text
C0947611 (UMLS CUI [1])
Item Group
Administrative
C1320722 (UMLS CUI-1)
oncologist; Signature
Item
Oncologist's Signature
text
C0259990 (UMLS CUI [1,1])
C1519316 (UMLS CUI [1,2])
Assessment Date
Item
Date of evaluation
date
C2985720 (UMLS CUI [1])
Terug naar het begin van de pagina 

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