ID

41129

Descrizione

A Study of CSL362 in Patients With CD123+ Acute Myeloid Leukemia Currently in Remission; ODM derived from: https://clinicaltrials.gov/show/NCT01632852

collegamento

https://clinicaltrials.gov/show/NCT01632852

Keywords

  1. 27/06/20 27/06/20 -
Titolare del copyright

See clinicaltrials.gov

Caricato su

27 giugno 2020

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY 4.0

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Eligibility Leukemia, Myeloid, Acute NCT01632852

Eligibility Leukemia, Myeloid, Acute NCT01632852

Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
male or female aged 18 years or older.
Descrizione

Age

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0001779
previous diagnosis of cd123+ acute myeloid leukemia (aml), de novo or secondary.
Descrizione

AML de novo CD123 Positive | Secondary Acute Myeloid Leukemia CD123 Positive

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0023467
UMLS CUI [1,2]
C1515568
UMLS CUI [1,3]
C1416408
UMLS CUI [1,4]
C1514241
UMLS CUI [2,1]
C0280449
UMLS CUI [2,2]
C1416408
UMLS CUI [2,3]
C1514241
completed and recovered from all planned induction and consolidation therapy according to the institution's standard of care, and achieved a complete remission (cr)/cr with incomplete platelet recovery (crp); either first or second cr.
Descrizione

Neoadjuvant Therapy Completed | Consolidation Therapy Completed | Patient recovered | In complete remission | Complete Response with Incomplete Platelet Recovery | Complete remission First | Complete remission second

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0600558
UMLS CUI [1,2]
C0205197
UMLS CUI [2,1]
C1511484
UMLS CUI [2,2]
C0205197
UMLS CUI [3]
C1115804
UMLS CUI [4]
C0677874
UMLS CUI [5]
C3890735
UMLS CUI [6,1]
C0677874
UMLS CUI [6,2]
C0205435
UMLS CUI [7,1]
C0677874
UMLS CUI [7,2]
C0205436
has factors conferring high risk of relapse.
Descrizione

Factor High risk of Relapse

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C1521761
UMLS CUI [1,2]
C0332167
UMLS CUI [1,3]
C0035020
no plans for additional post-remission chemotherapy.
Descrizione

Absence Chemotherapy Post Remission

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0332197
UMLS CUI [1,2]
C0392920
UMLS CUI [1,3]
C0687676
UMLS CUI [1,4]
C0544452
not currently a candidate for allogeneic hematopoietic stem cell transplant (hsct).
Descrizione

Patient Inappropriate Allogeneic hematopoietic stem cell transplant

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C1548788
UMLS CUI [1,3]
C4255274
Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
diagnosis of acute promyelocytic leukemia (apl).
Descrizione

Acute Promyelocytic Leukemia

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0023487
known leukemic involvement of the central nervous system.
Descrizione

Central Nervous System Involvement Leukemia

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C4050309
UMLS CUI [1,2]
C0023418
life expectancy 4 months or less as estimated by the investigator.
Descrizione

Life Expectancy

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0023671
concurrent treatment or planned treatment with other anticancer therapy (chemotherapy, immunotherapy, radiotherapy, targeted therapy, gene therapy).
Descrizione

Cancer treatment Other | Cancer treatment Other Planned | Chemotherapy | Immunotherapy | Therapeutic radiology procedure | Targeted Therapy | Gene therapy

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0920425
UMLS CUI [1,2]
C0205394
UMLS CUI [2,1]
C0920425
UMLS CUI [2,2]
C0205394
UMLS CUI [2,3]
C1301732
UMLS CUI [3]
C0392920
UMLS CUI [4]
C0021083
UMLS CUI [5]
C1522449
UMLS CUI [6]
C2985566
UMLS CUI [7]
C0017296

Similar models

Eligibility Leukemia, Myeloid, Acute NCT01632852

Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
male or female aged 18 years or older.
boolean
C0001779 (UMLS CUI [1])
AML de novo CD123 Positive | Secondary Acute Myeloid Leukemia CD123 Positive
Item
previous diagnosis of cd123+ acute myeloid leukemia (aml), de novo or secondary.
boolean
C0023467 (UMLS CUI [1,1])
C1515568 (UMLS CUI [1,2])
C1416408 (UMLS CUI [1,3])
C1514241 (UMLS CUI [1,4])
C0280449 (UMLS CUI [2,1])
C1416408 (UMLS CUI [2,2])
C1514241 (UMLS CUI [2,3])
Neoadjuvant Therapy Completed | Consolidation Therapy Completed | Patient recovered | In complete remission | Complete Response with Incomplete Platelet Recovery | Complete remission First | Complete remission second
Item
completed and recovered from all planned induction and consolidation therapy according to the institution's standard of care, and achieved a complete remission (cr)/cr with incomplete platelet recovery (crp); either first or second cr.
boolean
C0600558 (UMLS CUI [1,1])
C0205197 (UMLS CUI [1,2])
C1511484 (UMLS CUI [2,1])
C0205197 (UMLS CUI [2,2])
C1115804 (UMLS CUI [3])
C0677874 (UMLS CUI [4])
C3890735 (UMLS CUI [5])
C0677874 (UMLS CUI [6,1])
C0205435 (UMLS CUI [6,2])
C0677874 (UMLS CUI [7,1])
C0205436 (UMLS CUI [7,2])
Factor High risk of Relapse
Item
has factors conferring high risk of relapse.
boolean
C1521761 (UMLS CUI [1,1])
C0332167 (UMLS CUI [1,2])
C0035020 (UMLS CUI [1,3])
Absence Chemotherapy Post Remission
Item
no plans for additional post-remission chemotherapy.
boolean
C0332197 (UMLS CUI [1,1])
C0392920 (UMLS CUI [1,2])
C0687676 (UMLS CUI [1,3])
C0544452 (UMLS CUI [1,4])
Patient Inappropriate Allogeneic hematopoietic stem cell transplant
Item
not currently a candidate for allogeneic hematopoietic stem cell transplant (hsct).
boolean
C0030705 (UMLS CUI [1,1])
C1548788 (UMLS CUI [1,2])
C4255274 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
Acute Promyelocytic Leukemia
Item
diagnosis of acute promyelocytic leukemia (apl).
boolean
C0023487 (UMLS CUI [1])
Central Nervous System Involvement Leukemia
Item
known leukemic involvement of the central nervous system.
boolean
C4050309 (UMLS CUI [1,1])
C0023418 (UMLS CUI [1,2])
Life Expectancy
Item
life expectancy 4 months or less as estimated by the investigator.
boolean
C0023671 (UMLS CUI [1])
Cancer treatment Other | Cancer treatment Other Planned | Chemotherapy | Immunotherapy | Therapeutic radiology procedure | Targeted Therapy | Gene therapy
Item
concurrent treatment or planned treatment with other anticancer therapy (chemotherapy, immunotherapy, radiotherapy, targeted therapy, gene therapy).
boolean
C0920425 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
C0920425 (UMLS CUI [2,1])
C0205394 (UMLS CUI [2,2])
C1301732 (UMLS CUI [2,3])
C0392920 (UMLS CUI [3])
C0021083 (UMLS CUI [4])
C1522449 (UMLS CUI [5])
C2985566 (UMLS CUI [6])
C0017296 (UMLS CUI [7])

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