ID

44054

Description

Study part: Status of treatment blind. 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.

Keywords

  1. 6/19/18 6/19/18 -
  2. 9/20/21 9/20/21 -
Copyright Holder

GlaxoSmithKline

Uploaded on

September 20, 2021

DOI

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License

Creative Commons BY-NC 3.0

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Status of treatment blind Pazopanib Macular Degeneration MD1103367

Status of treatment blind

STATUS OF TREATMENT BLIND (Blind)
Description

STATUS OF TREATMENT BLIND (Blind)

Alias
UMLS CUI-1
C0749659
UMLS CUI-2
C2347038
Was the treatment blind broken during the study?
Description

Treatment Status; Blinded Clinical Study

Data type

text

Alias
UMLS CUI [1]
C0749659
UMLS CUI [2]
C2347038
Date/time blind broken
Description

Date and time Blinded Clinical Study study end

Data type

datetime

Alias
UMLS CUI [1,1]
C1264639
UMLS CUI [1,2]
C2347038
UMLS CUI [1,3]
C2983670
Reason blind broken
Description

Reason

Data type

text

Alias
UMLS CUI [1]
C0392360
Other, specify
Description

Other

Data type

text

Alias
UMLS CUI [1]
C0205394

Similar models

Status of treatment blind

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
STATUS OF TREATMENT BLIND (Blind)
C0749659 (UMLS CUI-1)
C2347038 (UMLS CUI-2)
Item
Was the treatment blind broken during the study?
text
C0749659 (UMLS CUI [1])
C2347038 (UMLS CUI [2])
Code List
Was the treatment blind broken during the study?
CL Item
No (N)
CL Item
Yes (Y)
Date and time Blinded Clinical Study study end
Item
Date/time blind broken
datetime
C1264639 (UMLS CUI [1,1])
C2347038 (UMLS CUI [1,2])
C2983670 (UMLS CUI [1,3])
Item
Reason blind broken
text
C0392360 (UMLS CUI [1])
Code List
Reason blind broken
CL Item
Medical emergency requiring identification of investigational product for further treatment (Medical emergency requiring identification of investigational product for further treatment)
CL Item
Other (Other)
Other
Item
Other, specify
text
C0205394 (UMLS CUI [1])

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