ID

23772

Descrição

Study part: Adverse Events Week 28. 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.

Palavras-chave

Versões (1)
  1. 12-07-17 12-07-17 -
Titular dos direitos

GlaxoSmithKline

Transferido a

12 juli 2017

DOI

Para um pedido faça login.

Licença

Creative Commons BY-NC 3.0
Comentários do modelo :

Aqui pode comentar o modelo. Pode comentá-lo especificamente através dos balões de texto nos grupos de itens e itens.

Voltar para os comentários do modelo
Comentários do grupo de itens para :

Comentários do item para :

  • Os mais recentes
  • Os mais antigos
  • Preferidos
  • Os mais recentes
    • Os mais recentes
    • Os mais antigos
    • Preferidos

Sem comentários

Para descarregar formulários, precisa de ter uma sessão iniciada. Por favor faça login ou registe-se gratuitamente.

Adverse Events Week 28 Mepolizumab HES NCT00086658

Inglês

Adverse Events Week 28

1 Formulários  
  1. StudyEvent: ODM
    1. Adverse Events Week 28
ADVERSE EVENTS
Descrição

ADVERSE EVENTS

Alias
UMLS CUI-1
C0877248 (Adverse event)
LOINC
MTHU014542
Any new study related non-serious adverse events/serious adverse events observed or reported by the subject or any changes to ongoing non-serious adverse events recorded in the appropriate Non-Serious Adverse Events/Serious Adverse Events section?
Descrição

Adverse Events

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0877248 (Adverse event)
LOINC
MTHU014542
Voltar ao início da página

Similar models

Adverse Events Week 28

1 Formulários
  1. StudyEvent: ODM
    1. Adverse Events Week 28
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
ADVERSE EVENTS
C0877248 (UMLS CUI-1)
Adverse Events
Item
Any new study related non-serious adverse events/serious adverse events observed or reported by the subject or any changes to ongoing non-serious adverse events recorded in the appropriate Non-Serious Adverse Events/Serious Adverse Events section?
boolean
C0877248 (UMLS CUI [1])
Voltar ao início da página 

Ajuda

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial