ID

31381

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

  1. 31-07-18 31-07-18 -
  2. 18-08-18 18-08-18 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

18 augustus 2018

DOI

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Licentie

Creative Commons BY-NC 3.0

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

Actual administered mCi Dose

Dosimetric Dose
Beschrijving

Dosimetric Dose

Alias
UMLS CUI-1
C4019308
Date dose administered
Beschrijving

Medication dose; Date in time

Datatype

date

Alias
UMLS CUI [1,1]
C4019308
UMLS CUI [1,2]
C0011008
Actual Iodine-131 Anti-B1 Antibody dose administered
Beschrijving

iodine-131-tositumomab; Medication dose

Datatype

text

Maateenheden
  • mCi
Alias
UMLS CUI [1,1]
C0768182
UMLS CUI [1,2]
C3174092
mCi
Therapeutic Dose
Beschrijving

Therapeutic Dose

Alias
UMLS CUI-1
C0087111
UMLS CUI-2
C0178602
Date Therapeutic Dose administered
Beschrijving

Date Therapeutic Dose administered

Datatype

date

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C0011008
Actual Iodine-131 Anti-B1 Antibody dose administered
Beschrijving

Actual Iodine-131 Anti-B1 Antibody dose administered

Datatype

text

Maateenheden
  • mCi
Alias
UMLS CUI [1,1]
C0768182
UMLS CUI [1,2]
C3174092
mCi
Administrative
Beschrijving

Administrative

Alias
UMLS CUI-1
C1320722
Investigator Signature
Beschrijving

Investigator Signature

Datatype

text

Alias
UMLS CUI [1]
C2346576
Date of evaluation
Beschrijving

Date of evaluation

Datatype

date

Alias
UMLS CUI [1]
C2985720

Similar models

Actual administered mCi Dose

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Dosimetric Dose
C4019308 (UMLS CUI-1)
Medication dose; Date in time
Item
Date dose administered
date
C4019308 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
iodine-131-tositumomab; Medication dose
Item
Actual Iodine-131 Anti-B1 Antibody dose administered
text
C0768182 (UMLS CUI [1,1])
C3174092 (UMLS CUI [1,2])
Item Group
Therapeutic Dose
C0087111 (UMLS CUI-1)
C0178602 (UMLS CUI-2)
Date Therapeutic Dose administered
Item
Date Therapeutic Dose administered
date
C0087111 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
Actual Iodine-131 Anti-B1 Antibody dose administered
Item
Actual Iodine-131 Anti-B1 Antibody dose administered
text
C0768182 (UMLS CUI [1,1])
C3174092 (UMLS CUI [1,2])
Item Group
Administrative
C1320722 (UMLS CUI-1)
Investigator Signature
Item
Investigator Signature
text
C2346576 (UMLS CUI [1])
Date of evaluation
Item
Date of evaluation
date
C2985720 (UMLS CUI [1])

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