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ID

22457

Description

Study part: Study conclusion.A Phase 2 Multicenter, Double-blind, Placebo-controlled, Study to to Evaluate the Corticosteroid- sparing effects of Mepolizumab in Subjects with Hypereosinophilic Syndromes (HES) and Evaluate Efficacy and Safety of Mepolizumab in Controlling the Clinical Signs and Symptoms of subjects with HES Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Sponsor: GlaxoSmithKline. Study ID: 100185, Clinical Study ID:MHE100185.

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Versions (1)
  1. 05/06/17 05/06/17 -
Détendeur de droits

GlaxoSmithKline

Téléchargé le

5 giugno 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0
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    Study conclusion Mepolizumab HES NCT00086658

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    Study conclusion

    1 Formulaires  
    1. StudyEvent: ODM
      1. Study conclusion
    STUDY CONCLUSION
    Description

    STUDY CONCLUSION

    Alias
    UMLS CUI-1
    C1707478
    UMLS CUI-2
    C0008972
    Subject ID
    Description

    Subject ID

    Type de données

    text

    Alias
    UMLS CUI [1]
    C2348585
    Date of subject completion or withdrawal
    Description

    Date of subject completion or withdrawal

    Type de données

    date

    Alias
    UMLS CUI [1]
    C2983670
    Was the subject withdrawn from the study?
    Description

    Study Subject Participation Status

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C2348568
    The primary reason for withdrawal:
    Description

    reason study conclusion

    Type de données

    text

    Alias
    UMLS CUI [1,1]
    C0392360
    UMLS CUI [1,2]
    C1707478
    UMLS CUI [1,3]
    C0008972
    If other, please specify
    Description

    Other

    Type de données

    text

    Alias
    UMLS CUI [1]
    C0205394
    Retour au début de la page

    Similar models

    Study conclusion

    1 Formulaires
    1. StudyEvent: ODM
      1. Study conclusion
    Name
    Type
    Description | Question | Decode (Coded Value)
    Type de données
    Alias
    Item Group
    STUDY CONCLUSION
    C1707478 (UMLS CUI-1)
    C0008972 (UMLS CUI-2)
    Subject ID
    Item
    Subject ID
    text
    C2348585 (UMLS CUI [1])
    Date of subject completion or withdrawal
    Item
    Date of subject completion or withdrawal
    date
    C2983670 (UMLS CUI [1])
    Study Subject Participation Status
    Item
    Was the subject withdrawn from the study?
    boolean
    C2348568 (UMLS CUI [1])
    Item
    The primary reason for withdrawal:
    text
    C0392360 (UMLS CUI [1,1])
    C1707478 (UMLS CUI [1,2])
    C0008972 (UMLS CUI [1,3])
    reason study conclusion
    Code List
    The primary reason for withdrawal:
    CL Item
    Adverse event (record details on the Non-Serious Adverse Event or Serious Adverse Event pages as appropriate) (Adverse event (record details on the Non-Serious Adverse Event or Serious Adverse Event pages as appropriate))
    C0877248 (UMLS CUI-1)
    CL Item
    Lost to follow-up (Lost to follow-up)
    C1302313 (UMLS CUI-1)
    CL Item
    Protocol violation (Protocol violation)
    C1709750 (UMLS CUI-1)
    CL Item
    Subject decided to withdraw from the study (Subject decided to withdraw from the study)
    C2348571 (UMLS CUI-1)
    CL Item
    Lack of efficacy (Lack of efficacy)
    C0235828 (UMLS CUI-1)
    CL Item
    Sponsor terminated study (Sponsor terminated study)
    C1710224 (UMLS CUI-1)
    CL Item
    Disease progression (Disease progression)
    C0242656 (UMLS CUI-1)
    CL Item
    Other, specify (Other, specify)
    C0205394 (UMLS CUI-1)
    Other
    Item
    If other, please specify
    text
    C0205394 (UMLS CUI [1])
    Retour au début de la page 

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