ID

44055

Descripción

Study documentation part: Pre-Treatment This is a phase III study of BMS-354825 in subjects with chronic myelogenous leukemia in accelerated phase, or in myeloid or lymphoid blast phase or with Philadelphia chromosome positive (Ph+) acute lymphoblastic leukemia who are resistant or intolerant to imatinib mesylate (Gleevec).Trial Number: NCT00123487. Drug: dasatinib. Phase 3.

Palabras clave

Versiones (4)
  1. 6/7/15 6/7/15 -
  2. 6/8/15 6/8/15 -
  3. 15/3/21 15/3/21 - Dr. rer. medic Philipp Neuhaus
  4. 20/9/21 20/9/21 -
Subido en

20 de septiembre de 2021

DOI

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Licencia

Creative Commons BY-NC 3.0 Legacy
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Advanced Chronic Myelogenous Leukemia (CML) NCT00123487 – Pre-Treatment

Inglés

Pre- treatment status

8 formularios  
PRE-TREATMENT STATUS
Descripción

PRE-TREATMENT STATUS

Will the subject enter the treatment phase of this study?
Descripción

WILL THE SUBJECT ENTER THE TREATMENT PHASE OF THIS STUDY ?

Tipo de datos

boolean

PRIMARY REASON FOR NOT ENTERING THE TREATMENT PHASE OF THIS STUDY (Fill only if study entry is denied)
Descripción

PRIMARY REASON FOR NOT ENTERING THE TREATMENT PHASE OF THIS STUDY (Fill only if study entry is denied)

Adverse event:
Descripción

ADVERSE EVENT

Tipo de datos

boolean

Alias
UMLS CUI-1
C0877248
Subject withdrew consent (specify):
Descripción

SUBJECT WITHDREW CONSENT (SPECIFY)

Tipo de datos

text

Alias
UMLS CUI-1
C0514044
UMLS CUI-2
C0805443
Death:
Descripción

DEATH

Tipo de datos

boolean

Alias
UMLS CUI-1
C0011065
Lost to Follow-up (Date of last contact):
Descripción

LOST TO FOLLOW-UP (DATE OF LAST CONTACT)

Tipo de datos

date

Alias
UMLS CUI-1
C0011008
Poor/ Non- compliance (specify):
Descripción

Poor/ Non- compliance (specify)

Tipo de datos

text

Alias
UMLS CUI-1
C1321605
Pregnancy:
Descripción

PREGNANCY

Tipo de datos

boolean

Alias
UMLS CUI-1
C0549206
Subject no longer meets study criteria (specify):
Descripción

SUBJECT NO LONGER MEETS STUDY CRITERIA (SPECIFY)

Tipo de datos

text

Administrative reason by sponsor:
Descripción

ADMINISTRATIVE REASON BY SPONSOR

Tipo de datos

boolean

Others (Specify):
Descripción

Others (Specify)

Tipo de datos

text

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Similar models

Pre- treatment status

8 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
PRE-TREATMENT STATUS
PRE-TREATMENT STATUS
Item
Will the subject enter the treatment phase of this study?
boolean
Item Group
PRIMARY REASON FOR NOT ENTERING THE TREATMENT PHASE OF THIS STUDY (Fill only if study entry is denied)
ADVERSE EVENT
Item
Adverse event:
boolean
C0877248 (UMLS CUI-1)
CONSENT
Item
Subject withdrew consent (specify):
text
C0514044 (UMLS CUI-1)
C0805443 (UMLS CUI-2)
DEATH
Item
Death:
boolean
C0011065 (UMLS CUI-1)
Date
Item
Lost to Follow-up (Date of last contact):
date
C0011008 (UMLS CUI-1)
COMPLIANCE
Item
Poor/ Non- compliance (specify):
text
C1321605 (UMLS CUI-1)
PREGNANCY
Item
Pregnancy:
boolean
C0549206 (UMLS CUI-1)
STUDY CRITERIA
Item
Subject no longer meets study criteria (specify):
text
ADMINISTRATIVE REASON BY SPONSOR
Item
Administrative reason by sponsor:
boolean
Others
Item
Others (Specify):
text
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