ID

13236

Description

A Safety Study of SGN-CD33A in AML Patients; ODM derived from: https://clinicaltrials.gov/show/NCT01902329

Link

https://clinicaltrials.gov/show/NCT01902329

Keywords

  1. 1/25/16 1/25/16 -
Copyright Holder

CC BY-NC 3.0

Uploaded on

January 25, 2016

DOI

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License

Creative Commons BY-NC 3.0

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Eligibility Acute Myelogenous Leukemia NCT01902329

Eligibility Acute Myelogenous Leukemia NCT01902329

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
acute myeloid leukemia, positive for cd33
Description

AML

Data type

boolean

Alias
UMLS CUI [1]
C0023467
eastern cooperative oncology group status of 0 or 1
Description

ECOG

Data type

boolean

Alias
UMLS CUI [1]
C1520224
adequate baseline renal and hepatic function
Description

renal and hepatic function

Data type

boolean

Alias
UMLS CUI [1,1]
C0232804
UMLS CUI [1,2]
C0232741
central venous access
Description

central venous access

Data type

boolean

Alias
UMLS CUI [1]
C1145640
either achieved complete remission (greater than 12 weeks in duration) with initial induction/consolidation and have experienced relapse of disease or declined treatment with high-dose induction/consolidation
Description

remission or relapse

Data type

boolean

Alias
UMLS CUI [1]
C0544452
UMLS CUI [2]
C0277556
bone marrow blasts greater than or equal to 5% for relapsed patients, or greater than or equal to 20% for untreated patients
Description

bone marrow blasts

Data type

boolean

Alias
UMLS CUI [1]
C0368761
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
inadequate lung function
Description

pulmonary function

Data type

boolean

Alias
UMLS CUI [1]
C0231921
prior allogeneic stem cell transplant, except for a specific cohort
Description

stem cell transplant

Data type

boolean

Alias
UMLS CUI [1]
C1504389
high-dose chemotherapy within 4 weeks of study drug
Description

chemotherapy

Data type

boolean

Alias
UMLS CUI [1]
C0392920
antileukemia treatment within 14 days of study drug (other than hydroxyurea or 6-mercaptopurine)
Description

antileukemia treatment

Data type

boolean

Alias
UMLS CUI [1]
C0087111

Similar models

Eligibility Acute Myelogenous Leukemia NCT01902329

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
AML
Item
acute myeloid leukemia, positive for cd33
boolean
C0023467 (UMLS CUI [1])
ECOG
Item
eastern cooperative oncology group status of 0 or 1
boolean
C1520224 (UMLS CUI [1])
renal and hepatic function
Item
adequate baseline renal and hepatic function
boolean
C0232804 (UMLS CUI [1,1])
C0232741 (UMLS CUI [1,2])
central venous access
Item
central venous access
boolean
C1145640 (UMLS CUI [1])
remission or relapse
Item
either achieved complete remission (greater than 12 weeks in duration) with initial induction/consolidation and have experienced relapse of disease or declined treatment with high-dose induction/consolidation
boolean
C0544452 (UMLS CUI [1])
C0277556 (UMLS CUI [2])
bone marrow blasts
Item
bone marrow blasts greater than or equal to 5% for relapsed patients, or greater than or equal to 20% for untreated patients
boolean
C0368761 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
pulmonary function
Item
inadequate lung function
boolean
C0231921 (UMLS CUI [1])
stem cell transplant
Item
prior allogeneic stem cell transplant, except for a specific cohort
boolean
C1504389 (UMLS CUI [1])
chemotherapy
Item
high-dose chemotherapy within 4 weeks of study drug
boolean
C0392920 (UMLS CUI [1])
antileukemia treatment
Item
antileukemia treatment within 14 days of study drug (other than hydroxyurea or 6-mercaptopurine)
boolean
C0087111 (UMLS CUI [1])

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