ID

30801

Descripción

Study part: Treatment confirmation. A phase 1 single-masked, randomized (with respect to placebo), placebo-controlled, parallel-group, dose-rising study to evaluate the safety, tolerability and pharmacokinetics of repeat oral doses of GW786034 in elderly healthy volunteers. Trade Name: Votrient. Clinical Study ID: MD1103367.

Palabras clave

  1. 20/6/18 20/6/18 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

20 de junio de 2018

DOI

Para solicitar uno, por favor iniciar sesión.

Licencia

Creative Commons BY-NC 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.

Treatment confirmation Pazopanib Macular Degeneration MD1103367

Treatment confirmation

  1. StudyEvent: ODM
    1. Treatment confirmation
TREATMENT CONFIRMATION (Trt Cont)
Descripción

TREATMENT CONFIRMATION (Trt Cont)

Alias
UMLS CUI-1
C0087111
UMLS CUI-2
C0750484
Did the subject receive the correct treatment (e.g., treatment which the subject was assigned to) during this dosing interval?
Descripción

therapy assigned

Tipo de datos

text

Alias
UMLS CUI [1]
C1522541
When no, record reason
Descripción

reason therapy assigned

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0392360
UMLS CUI [1,2]
C1522541

Similar models

Treatment confirmation

  1. StudyEvent: ODM
    1. Treatment confirmation
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
TREATMENT CONFIRMATION (Trt Cont)
C0087111 (UMLS CUI-1)
C0750484 (UMLS CUI-2)
Item
Did the subject receive the correct treatment (e.g., treatment which the subject was assigned to) during this dosing interval?
text
C1522541 (UMLS CUI [1])
Code List
Did the subject receive the correct treatment (e.g., treatment which the subject was assigned to) during this dosing interval?
CL Item
Yes (Y)
CL Item
No (N)
reason therapy assigned
Item
When no, record reason
text
C0392360 (UMLS CUI [1,1])
C1522541 (UMLS CUI [1,2])

Utilice este formulario para comentarios, preguntas y sugerencias.

Los campos marcados con * son obligatorios.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial