ID
13744
Description
A Study of AS1411 Combined With Cytarabine in the Treatment of Patients With Primary Refractory or Relapsed Acute Myeloid Leukemia; ODM derived from: https://clinicaltrials.gov/show/NCT01034410
Lien
https://clinicaltrials.gov/show/NCT01034410
Mots-clés
Versions (1)
- 02/03/2016 02/03/2016 -
Détendeur de droits
CC BY-NC 3.0
Téléchargé le
2 mars 2016
DOI
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Licence
Creative Commons BY-NC 3.0
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Eligibility Acute Myeloid Leukemia NCT01034410
Eligibility Acute Myeloid Leukemia NCT01034410
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Description
an initial diagnosis of acute promyelocytic leukemia (as defined by french-american-british criteria (bennett 1976))
Type de données
boolean
Alias
- UMLS CUI [1]
- C0023487
Description
secondary aml, defined as aml evolving from antecedent hematological disorder or prior exposure to leukemogenic therapy or agent
Type de données
boolean
Alias
- UMLS CUI [1]
- C0280449
Description
clinically active cns leukemia
Type de données
boolean
Alias
- UMLS CUI [1]
- C1332884
Description
previously received a total cumulative dose of cytarabine > 6g/m2 in the last 6 months
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0010711
- UMLS CUI [1,2]
- C2986497
Description
previously received > 1 induction regimen (defined as 1 or 2 cycles of a drug or a drug combination administered as remission induction therapy)
Type de données
boolean
Alias
- UMLS CUI [1]
- C3179010
Similar models
Eligibility Acute Myeloid Leukemia NCT01034410
- StudyEvent: Eligibility
C0205269 (UMLS CUI [1,2])
C0205269 (UMLS CUI [1,2])
C1982687 (UMLS CUI [2])
C0023467 (UMLS CUI [2,1])
C0277556 (UMLS CUI [2,2])
C2986497 (UMLS CUI [1,2])