ID

19059

Description

Phase I study of panobinostat and imatinib in patients with treatment-refractory metastatic gastrointestinal stromal tumors WTZ-GIST-09-01 (EudraCT number: 2009-011417-24; German Clinical Trials Register: DRKS00000657) was approved by the institutional ethics committees of the two participating centers and the German Federal Regulatory Drug Agency (BfArM; 4035954).

Keywords

Versions (1)
  1. 12/2/16 12/2/16 -
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December 2, 2016

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Creative Commons BY-NC-ND 3.0
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WTZ-GIST-09-01 (Imatinib + LBH589) Concomitant Therapies 2009-011417-24 DRKS00000657

English

WTZ-GIST-09-01 (Imatinib + LBH589) Concomitant Therapies 2009-011417-24

1 forms  
Concomitant Therapies
Description

Concomitant Therapies

Alias
UMLS CUI-1
C1707479
The patient did not get any concomitant therapy for the whole study period?
Description

Concomitant Therapies

Data type

boolean

Alias
UMLS CUI [1]
C1707479
Nr.
Description

Concomitant Therapies: Number

Data type

integer

Alias
UMLS CUI [1,1]
C0449788
UMLS CUI [1,2]
C1707479
Concomitant therapy name
Description

Concomitant Therapies: Name

Data type

text

Alias
UMLS CUI [1,1]
C0027365
UMLS CUI [1,2]
C1707479
Concomitant therapy dosage
Description

Concomitant Therapies: Dosage

Data type

float

Alias
UMLS CUI [1,1]
C0178602
UMLS CUI [1,2]
C1707479
Indication: note the number if necessary
Description

Concomitant Therapies: Indication

Data type

integer

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C1707479
Onset of therapy
Description

Concomitant Therapies: Onset

Data type

date

Measurement units
  • YYYY-MM-DD
Alias
UMLS CUI [1,1]
C0574845
UMLS CUI [1,2]
C1707479
YYYY-MM-DD
End of therapy
Description

Concomitant Therapies: End Date

Data type

date

Measurement units
  • YYYY-MM-DD
Alias
UMLS CUI [1,1]
C0806020
UMLS CUI [1,2]
C1707479
YYYY-MM-DD
Continuing?
Description

Concomitant Therapies: Ongoing

Data type

boolean

Alias
UMLS CUI [1,1]
C0549178
UMLS CUI [1,2]
C1707479
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Similar models

WTZ-GIST-09-01 (Imatinib + LBH589) Concomitant Therapies 2009-011417-24

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Concomitant Therapies
C1707479 (UMLS CUI-1)
Concomitant Therapies
Item
The patient did not get any concomitant therapy for the whole study period?
boolean
C1707479 (UMLS CUI [1])
Concomitant Therapies: Number
Item
Nr.
integer
C0449788 (UMLS CUI [1,1])
C1707479 (UMLS CUI [1,2])
Concomitant Therapies: Name
Item
Concomitant therapy name
text
C0027365 (UMLS CUI [1,1])
C1707479 (UMLS CUI [1,2])
Concomitant Therapies: Dosage
Item
Concomitant therapy dosage
float
C0178602 (UMLS CUI [1,1])
C1707479 (UMLS CUI [1,2])
Concomitant Therapies: Indication
Item
Indication: note the number if necessary
integer
C3146298 (UMLS CUI [1,1])
C1707479 (UMLS CUI [1,2])
Concomitant Therapies: Onset
Item
Onset of therapy
date
C0574845 (UMLS CUI [1,1])
C1707479 (UMLS CUI [1,2])
Concomitant Therapies: End Date
Item
End of therapy
date
C0806020 (UMLS CUI [1,1])
C1707479 (UMLS CUI [1,2])
Concomitant Therapies: Ongoing
Item
Continuing?
boolean
C0549178 (UMLS CUI [1,1])
C1707479 (UMLS CUI [1,2])
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