Informatie:
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ID
13236
Beschrijving
A Safety Study of SGN-CD33A in AML Patients; ODM derived from: https://clinicaltrials.gov/show/NCT01902329
Link
https://clinicaltrials.gov/show/NCT01902329
Trefwoorden
Versies (1)
- 25-01-16 25-01-16 -
Houder van rechten
CC BY-NC 3.0
Geüploaded op
25 januari 2016
DOI
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Licentie
Creative Commons BY-NC 3.0
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Eligibility Acute Myelogenous Leukemia NCT01902329
Eligibility Acute Myelogenous Leukemia NCT01902329
- StudyEvent: Eligibility
Similar models
Eligibility Acute Myelogenous Leukemia NCT01902329
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
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])
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])
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])
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])