ID

31386

Description

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

Mots-clés

  1. 06/08/2018 06/08/2018 -
  2. 18/08/2018 18/08/2018 -
Détendeur de droits

GlaxoSmithKline

Téléchargé le

18 août 2018

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0

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Iodine-131 Anti-B1 Antibody for Non Hodgkin’s Lymphomas NCT00996593

Independent Response Evaluation Joint Assessment and Consensus Criteria

Independent Response Evaluation
Description

Independent Response Evaluation

Alias
UMLS CUI-1
C0521982
UMLS CUI-2
C4277662
Date of Response
Description

Date of Response

Type de données

date

Alias
UMLS CUI [1,1]
C0521982
UMLS CUI [1,2]
C0011008
Joint Response Assessment
Description

Response to treatment | Evaluation | Common (qualifier value)

Type de données

text

Alias
UMLS CUI [1,1]
C0521982
UMLS CUI [1,2]
C0220825
UMLS CUI [1,3]
C0205214
Comments
Description

Comments

Type de données

text

Alias
UMLS CUI [1]
C0947611
Consensus Criteria
Description

Consensus Criteria

Alias
UMLS CUI-1
C0376298
UMLS CUI-2
C0243161
Date of Response
Description

Date of Response

Type de données

date

Alias
UMLS CUI [1,1]
C0521982
UMLS CUI [1,2]
C0011008
Joint Response Assessment
Description

Response to treatment | Evaluation | Common (qualifier value)

Type de données

text

Alias
UMLS CUI [1,1]
C0521982
UMLS CUI [1,2]
C0220825
UMLS CUI [1,3]
C0205214
Comments
Description

Comments

Type de données

text

Alias
UMLS CUI [1]
C0947611
Administrative
Description

Administrative

Alias
UMLS CUI-1
C1320722
Radiologist's Signature
Description

radiologist; Signature

Type de données

text

Alias
UMLS CUI [1,1]
C1519316
UMLS CUI [1,2]
C0260194
Date of Evaluation Radiologist
Description

radiologist; Assessment Date

Type de données

date

Alias
UMLS CUI [1,1]
C0260194
UMLS CUI [1,2]
C2985720
Oncologist's Signature
Description

oncologist ;Signature

Type de données

text

Alias
UMLS CUI [1,1]
C0259990
UMLS CUI [1,2]
C1519316
Date of Evaluation Oncologist
Description

oncologist; Assessment Date

Type de données

text

Alias
UMLS CUI [1,1]
C0259990
UMLS CUI [1,2]
C2985720

Similar models

Independent Response Evaluation Joint Assessment and Consensus Criteria

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Independent Response Evaluation
C0521982 (UMLS CUI-1)
C4277662 (UMLS CUI-2)
Date of Response
Item
Date of Response
date
C0521982 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item
Joint Response Assessment
text
C0521982 (UMLS CUI [1,1])
C0220825 (UMLS CUI [1,2])
C0205214 (UMLS CUI [1,3])
CL Item
CR  (5)
CL Item
CCR  (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
Consensus Criteria
C0376298 (UMLS CUI-1)
C0243161 (UMLS CUI-2)
Date of Response
Item
Date of Response
date
C0521982 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item
Joint Response Assessment
text
C0521982 (UMLS CUI [1,1])
C0220825 (UMLS CUI [1,2])
C0205214 (UMLS CUI [1,3])
CL Item
CR (5)
CL Item
CCR (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)
radiologist; Signature
Item
Radiologist's Signature
text
C1519316 (UMLS CUI [1,1])
C0260194 (UMLS CUI [1,2])
radiologist; Assessment Date
Item
Date of Evaluation Radiologist
date
C0260194 (UMLS CUI [1,1])
C2985720 (UMLS CUI [1,2])
oncologist ;Signature
Item
Oncologist's Signature
text
C0259990 (UMLS CUI [1,1])
C1519316 (UMLS CUI [1,2])
oncologist; Assessment Date
Item
Date of Evaluation Oncologist
text
C0259990 (UMLS CUI [1,1])
C2985720 (UMLS CUI [1,2])

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