ID

22456

Beskrivning

Study part: Pregnancy Information 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.

Nyckelord

Pregnancy Tests

2017-06-05 2017-06-05 -

Rättsinnehavare

GlaxoSmithKline

Uppladdad den

5 juni 2017

DOI

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Licens

Creative Commons BY-NC 3.0

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Pregnancy Information Study Conclusion Mepolizumab HES NCT00086658

model
Detaljer

Pregnancy Information Study Conclusion

StudyEvent: ODM
1. Pregnancy Information Study Conclusion

PREGNANCY INFORMATION

Beskrivning

PREGNANCY INFORMATION

Alias

UMLS CUI-1: C0032961

Did the subject become pregnant during the study?

Beskrivning

pregnancy

Datatyp

text

Alias

UMLS CUI [1]: C0032961

Yes (If Yes, complete Pregnancy Notification form.) (Yes (If Yes, complete Pregnancy Notification form.))

No (No)

Not Applicable (not of childbearing potential or male) (Not Applicable (not of childbearing potential or male))

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Pregnancy Information Study Conclusion

StudyEvent: ODM
1. Pregnancy Information Study Conclusion

Name

Typ

Description | Question | Decode (Coded Value)

Datatyp

Alias

PREGNANCY INFORMATION

Item Group

PREGNANCY INFORMATION

C0032961 (UMLS CUI-1)

Item

Did the subject become pregnant during the study?

text

C0032961 (UMLS CUI [1])

Code List

Did the subject become pregnant during the study?

CL Item

Yes (If Yes, complete Pregnancy Notification form.) (Yes (If Yes, complete Pregnancy Notification form.))

CL Item

No (No)

CL Item

Not Applicable (not of childbearing potential or male) (Not Applicable (not of childbearing potential or male))

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