Información:
Error:
ID
19051
Descripción
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).
Palabras clave
Versiones (1)
- 1/12/16 1/12/16 -
Subido en
1 de diciembre de 2016
DOI
Para solicitar uno, por favor iniciar sesión.
Licencia
Creative Commons BY-NC-ND 3.0
Comentarios del modelo :
Puede comentar sobre el modelo de datos aquí. A través de las burbujas de diálogo en los grupos de elementos y elementos, puede agregar comentarios específicos.
Comentarios de grupo de elementos para :
Comentarios del elemento para :
Para descargar modelos de datos, debe haber iniciado sesión. Por favor iniciar sesión o Registrate gratis.
WTZ-GIST-09-01 (Imatinib + LBH589) Additional Cycle 2009-011417-24 DRKS00000657
WTZ-GIST-09-01 (Imatinib + LBH589) Additional Cycle 2009-011417-24
Similar models
WTZ-GIST-09-01 (Imatinib + LBH589) Additional Cycle 2009-011417-24
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Cycle Week
Item
Cycle Week Number: V_
integer
C1302181 (UMLS CUI [1,1])
C0449788 (UMLS CUI [1,2])
C0449788 (UMLS CUI [1,2])
Start Day
Item
Start of cycle
date
C0808070 (UMLS CUI [1])
Body Weight
Item
Weight
float
C0005910 (UMLS CUI [1])
Systolic Blood Pressure
Item
Syst.
integer
C0871470 (UMLS CUI [1])
Diastolic Blood Pressure
Item
Diast.
integer
C0428883 (UMLS CUI [1])
Heart rate
Item
Pulse
integer
C0018810 (UMLS CUI [1])
Body temperature
Item
Temperature
float
C0005903 (UMLS CUI [1])
ECG
Item
ECG
text
C1623258 (UMLS CUI [1])
Physical Examination
Item
Physical Examination
text
C0031809 (UMLS CUI [1])
Adverse Event
Item
Adverse Event
text
C0877248 (UMLS CUI [1])
Dose-limiting toxicity
Item
DLT
text
C1512043 (UMLS CUI [1,1])
C0013221 (UMLS CUI [1,2])
C0013221 (UMLS CUI [1,2])
Concomitant Medication
Item
Concomitant Medication
text
C2347852 (UMLS CUI [1])
ECOG status
Item
ECOG
text
C1520224 (UMLS CUI [1])
Haematology assessment
Item
Haematology
text
C0474523 (UMLS CUI [1])
Urinanalysis
Item
Urinanalysis
text
C0042014 (UMLS CUI [1])
Biochemistry assessment
Item
Biochemistry
text
C0005477 (UMLS CUI [1,1])
C0220825 (UMLS CUI [1,2])
C0220825 (UMLS CUI [1,2])