ID

31864

Beschrijving

Study ID: 105229 Clinical Study ID: GLP105229 Study Title: A double-blinded, randomized, placebo-controlled, staggered-parallel, escalating dose study to investigate the safety, tolerability, pharmacokinetics and pharmacodynamics of subcutaneous injections of GSK 716155 in healthy volunteers. Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: albiglutide Trade Name: Tanzeum,Eperzan Study Indication: Diabetes Mellitus, Type 2

Trefwoorden

Versies (1)
  1. 05-10-18 05-10-18 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

5 oktober 2018

DOI

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Licentie

Creative Commons BY-NC 3.0
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Subcutaneous injections of GSK 716155 in healthy volunteers; Study ID: 105229

Engels

Pregnancy Information

1 Formulieren  
  1. StudyEvent: ODM
    1. Pregnancy Information
Pregnancy Information
Beschrijving

Pregnancy Information

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

Pregnancy, During, Clinical Trial Period

Datatype

text

Alias
UMLS CUI [1,1]
C0032961
UMLS CUI [1,2]
C0347984
UMLS CUI [1,3]
C2347804
Did a female partner of the male subject become pregnant during the study?
Beschrijving

Pregnancy of partner, During; Clinical Trial Period

Datatype

text

Alias
UMLS CUI [1,1]
C0919624
UMLS CUI [1,2]
C0347984
UMLS CUI [1,3]
C2347804
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Similar models

Pregnancy Information

1 Formulieren
  1. StudyEvent: ODM
    1. Pregnancy Information
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Pregnancy Information
C0032961 (UMLS CUI-1)
C1533716 (UMLS CUI-2)
Item
Did the subject become pregnant during the study?
text
C0032961 (UMLS CUI [1,1])
C0347984 (UMLS CUI [1,2])
C2347804 (UMLS CUI [1,3])
Pregnancy, During, Clinical Trial Period
Code List
Did the subject become pregnant during the study?
CL Item
Yes (Yes)
CL Item
No (No)
CL Item
Not applicable (not of childbearing potential or male) (Not applicable (not of childbearing potential or male))
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])
C2347804 (UMLS CUI [1,3])
Pregnancy of partner, During; Clinical Trial Period
Code List
Did a female partner of the male subject become pregnant during the study?
CL Item
Yes (Yes)
CL Item
No (No)
CL Item
Not Applicable (subject is female, female partner not of childbearing potential or no female partner) (Not Applicable (subject is female, female partner not of childbearing potential or no female partner))
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