0 Avaliações
ID

31865

Descrição

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

Palavras-chave

Versões (1)
  1. 05/10/2018 05/10/2018 -
Titular dos direitos

GlaxoSmithCline

Transferido a

5 de outubro de 2018

DOI

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Licença

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

    Inglês

    Study Conclusion

    1 Formulários  
    1. StudyEvent: ODM
      1. Study Conclusion
    Study Conclusion
    Descrição

    Study Conclusion

    Alias
    UMLS CUI-1
    C1707478 (Conclusion)
    UMLS CUI-2
    C0008976 (Clinical Trials)
    SNOMED
    110465008
    LOINC
    LP231796-6
    Study Conclusion
    Descrição

    Study Conclusion

    Alias
    UMLS CUI-1
    C1707478 (Conclusion)
    UMLS CUI-2
    C0008976 (Clinical Trials)
    SNOMED
    110465008
    LOINC
    LP231796-6
    Date of subject completion or withdrawal
    Descrição

    Study End Date; Patient withdrawn from study, date in time

    Tipo de dados

    date

    Alias
    UMLS CUI [1]
    C2983670 (Study End Date)
    UMLS CUI [2,1]
    C0422727 (Patient withdrawn from trial)
    SNOMED
    185924006
    UMLS CUI [2,2]
    C0011008 (Date in time)
    SNOMED
    410671006
    Was the subject withdrawn from the study?
    Descrição

    Patient withdrawn from trial

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1]
    C0422727 (Patient withdrawn from trial)
    SNOMED
    185924006
    Primary reason for withdrawal
    Descrição

    Patient withdrawn from study; Indication

    Tipo de dados

    text

    Alias
    UMLS CUI [1,1]
    C0422727 (Patient withdrawn from trial)
    SNOMED
    185924006
    UMLS CUI [1,2]
    C0392360 (Indication of (contextual qualifier))
    SNOMED
    230165009
    LOINC
    MTHU008319
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    Similar models

    Study Conclusion

    1 Formulários
    1. StudyEvent: ODM
      1. Study Conclusion
    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de dados
    Alias
    Item Group
    Study Conclusion
    C1707478 (UMLS CUI-1)
    C0008976 (UMLS CUI-2)
    Item Group
    Study Conclusion
    C1707478 (UMLS CUI-1)
    C0008976 (UMLS CUI-2)
    Study End Date; Patient withdrawn from study, date in time
    Item
    Date of subject completion or withdrawal
    date
    C2983670 (UMLS CUI [1])
    C0422727 (UMLS CUI [2,1])
    C0011008 (UMLS CUI [2,2])
    Patient withdrawn from trial
    Item
    Was the subject withdrawn from the study?
    boolean
    C0422727 (UMLS CUI [1])
    Item
    Primary reason for withdrawal
    text
    C0422727 (UMLS CUI [1,1])
    C0392360 (UMLS CUI [1,2])
    Patient withdrawn from study; Indication
    Code List
    Primary reason for withdrawal
    CL Item
    Adverse event (Adverse event)
    CL Item
    Lost to follow-up (Lost to follow-up)
    CL Item
    Protocol violation (Protocol violation)
    CL Item
    Subject decided to withdraw from the study (Subject decided to withdraw from the study)
    CL Item
    Sponsor terminated study (Sponsor terminated study)
    CL Item
    Hypoglycaemic event (Hypoglycaemic event)
    CL Item
    Other, specify (Other, specify)
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