ID
13744
Descripción
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
Link
https://clinicaltrials.gov/show/NCT01034410
Palabras clave
Versiones (1)
- 2/3/16 2/3/16 -
Titular de derechos de autor
CC BY-NC 3.0
Subido en
2 de marzo de 2016
DOI
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Licencia
Creative Commons BY-NC 3.0
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Eligibility Acute Myeloid Leukemia NCT01034410
Eligibility Acute Myeloid Leukemia NCT01034410
- StudyEvent: Eligibility
Descripción
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Descripción
an initial diagnosis of acute promyelocytic leukemia (as defined by french-american-british criteria (bennett 1976))
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0023487
Descripción
secondary aml, defined as aml evolving from antecedent hematological disorder or prior exposure to leukemogenic therapy or agent
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0280449
Descripción
clinically active cns leukemia
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C1332884
Descripción
previously received a total cumulative dose of cytarabine > 6g/m2 in the last 6 months
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0010711
- UMLS CUI [1,2]
- C2986497
Descripción
previously received > 1 induction regimen (defined as 1 or 2 cycles of a drug or a drug combination administered as remission induction therapy)
Tipo de datos
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])