ID

30759

Beschrijving

Study part: Study Conclusion. 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.

Trefwoorden

Versies (2)
  1. 19-06-18 19-06-18 -
  2. 20-09-21 20-09-21 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

19 juni 2018

DOI

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Licentie

Creative Commons BY-NC 3.0
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Study Conclusion Pazopanib Macular Degeneration MD1103367

Engels

Study Conclusion

1 Formulieren  
  1. StudyEvent: ODM
    1. Study Conclusion
STUDY CONCLUSION (Conclusion)
Beschrijving

STUDY CONCLUSION (Conclusion)

Alias
UMLS CUI-1
C1707478
UMLS CUI-2
C0008976
Date/time of subject completion or withdrawal
Beschrijving

Date and time Study Conclusion

Datatype

datetime

Alias
UMLS CUI [1,1]
C1717740
UMLS CUI [1,2]
C1707478
UMLS CUI [1,3]
C0008976
Was the subject withdrawn from the study?
Beschrijving

Study Withdrawn

Datatype

text

Alias
UMLS CUI [1]
C2348571
Specify primary reason for withdrawal
Beschrijving

reason study withdrawn

Datatype

text

Alias
UMLS CUI [1,1]
C0392360
UMLS CUI [1,2]
C2348571
Other, specify
Beschrijving

other

Datatype

text

Alias
UMLS CUI [1]
C0205394
Case book ready for signature
Beschrijving

Case book ready for signature

Datatype

text

Alias
UMLS CUI [1]
C1519316
Terug naar het begin van de pagina

Similar models

Study Conclusion

1 Formulieren
  1. StudyEvent: ODM
    1. Study Conclusion
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
STUDY CONCLUSION (Conclusion)
C1707478 (UMLS CUI-1)
C0008976 (UMLS CUI-2)
Date and time Study Conclusion
Item
Date/time of subject completion or withdrawal
datetime
C1717740 (UMLS CUI [1,1])
C1707478 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
Item
Was the subject withdrawn from the study?
text
C2348571 (UMLS CUI [1])
Study Withdrawn
Code List
Was the subject withdrawn from the study?
CL Item
No (N)
CL Item
Yes (Y)
Item
Specify primary reason for withdrawal
text
C0392360 (UMLS CUI [1,1])
C2348571 (UMLS CUI [1,2])
reason study withdrawn
Code List
Specify primary reason for withdrawal
CL Item
Adverse event  (1)
C0877248 (UMLS CUI-1)
(Comment:en)
CL Item
Lost to follow-up  (2)
C1302313 (UMLS CUI-1)
(Comment:en)
CL Item
Protocol violation  (3)
C1709750 (UMLS CUI-1)
(Comment:en)
CL Item
Subject decided to withdraw from the study  (4)
C1710677 (UMLS CUI-1)
(Comment:en)
CL Item
Sponsor terminated study  (6)
C1710224 (UMLS CUI-1)
(Comment:en)
CL Item
Other (Z)
C0205394 (UMLS CUI-1)
(Comment:en)
other
Item
Other, specify
text
C0205394 (UMLS CUI [1])
Item
Case book ready for signature
text
C1519316 (UMLS CUI [1])
Study Withdrawn
Code List
Case book ready for signature
CL Item
No (N)
CL Item
Yes (Y)
Terug naar het begin van de pagina 

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