ID

44055

Description

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.

Mots-clés

Versions (4)
  1. 06/07/2015 06/07/2015 -
  2. 06/08/2015 06/08/2015 -
  3. 15/03/2021 15/03/2021 - Dr. rer. medic Philipp Neuhaus
  4. 20/09/2021 20/09/2021 -
Téléchargé le

20 septembre 2021

DOI

Pour une demande vous connecter.

Licence

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

Anglais

Pre- treatment status

8 Formulaires  
PRE-TREATMENT STATUS
Description

PRE-TREATMENT STATUS

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

WILL THE SUBJECT ENTER THE TREATMENT PHASE OF THIS STUDY ?

Type de données

boolean

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

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

Adverse event:
Description

ADVERSE EVENT

Type de données

boolean

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

SUBJECT WITHDREW CONSENT (SPECIFY)

Type de données

text

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

DEATH

Type de données

boolean

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

LOST TO FOLLOW-UP (DATE OF LAST CONTACT)

Type de données

date

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

Poor/ Non- compliance (specify)

Type de données

text

Alias
UMLS CUI-1
C1321605
Pregnancy:
Description

PREGNANCY

Type de données

boolean

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

SUBJECT NO LONGER MEETS STUDY CRITERIA (SPECIFY)

Type de données

text

Administrative reason by sponsor:
Description

ADMINISTRATIVE REASON BY SPONSOR

Type de données

boolean

Others (Specify):
Description

Others (Specify)

Type de données

text

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Similar models

Pre- treatment status

8 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
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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