ID

30758

Description

Study part: Pregnancy Information. 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.

Mots-clés

  1. 19/06/2018 19/06/2018 -
Détendeur de droits

GlaxoSmithKline

Téléchargé le

19 juin 2018

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0

Modèle Commentaires :

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Pregnancy Information Pazopanib Macular Degeneration MD1103367

Pregnancy Information

  1. StudyEvent: ODM
    1. Pregnancy Information
PREGNANCY INFORMATION (Preg M)
Description

PREGNANCY INFORMATION (Preg M)

Alias
UMLS CUI-1
C0032961
UMLS CUI-2
C1533716
UMLS CUI-3
C0086582
Did a female partner of the male subject become pregnant during the study?
Description

Female partner pregnant

Type de données

text

Alias
UMLS CUI [1,1]
C0919624
UMLS CUI [1,2]
C0347984
UMLS CUI [1,3]
C0008972
PREGNANCY INFORMATION (Preg F)
Description

PREGNANCY INFORMATION (Preg F)

Alias
UMLS CUI-1
C0032961
UMLS CUI-2
C1533716
UMLS CUI-3
C0086287
Did the subject become pregnant during the study?
Description

pregnancy

Type de données

text

Alias
UMLS CUI [1]
C0032961

Similar models

Pregnancy Information

  1. StudyEvent: ODM
    1. Pregnancy Information
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
PREGNANCY INFORMATION (Preg M)
C0032961 (UMLS CUI-1)
C1533716 (UMLS CUI-2)
C0086582 (UMLS CUI-3)
Item
Did a female partner of the male subject become pregnant during the study?
text
C0919624 (UMLS CUI [1,1])
C0347984 (UMLS CUI [1,2])
C0008972 (UMLS CUI [1,3])
Code List
Did a female partner of the male subject become pregnant during the study?
CL Item
No (N)
CL Item
Yes (Y)
CL Item
Not Applicable (X)
Item Group
PREGNANCY INFORMATION (Preg F)
C0032961 (UMLS CUI-1)
C1533716 (UMLS CUI-2)
C0086287 (UMLS CUI-3)
Item
Did the subject become pregnant during the study?
text
C0032961 (UMLS CUI [1])
Code List
Did the subject become pregnant during the study?
CL Item
No (N)
CL Item
Yes (Y)

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