ID

38749

Descripción

Study ID: 109035 Clinical Study ID: 109035 Study Title: A Randomised, Double-Blind, Parallel-Group, Placebo-Controlled Study Evaluating the Efficacy and Safety of GSK163090 in Subjects With Major Depressive Disorder Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00896363 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: GSK163090 1 mg, GSK163090 Placebo, GSK163090 3 mg Trade Name: Study Indication: Depressive Disorder

Palabras clave

  1. 31/10/19 31/10/19 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

31 de octubre de 2019

DOI

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Licencia

Creative Commons BY-NC 3.0

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Efficacy and Safety of GSK163090 in Subjects with Major Depressive Disorder; NCT00896363

Dose Reduction

  1. StudyEvent: ODM
    1. Dose Reduction
Dose Reduction Due to Adverse Experiences
Descripción

Dose Reduction Due to Adverse Experiences

Alias
UMLS CUI-1
C1707814
Date of decision to reduce the dose
Descripción

Dose Reduced, Decision, Date in time

Tipo de datos

date

Alias
UMLS CUI [1,1]
C1707814
UMLS CUI [1,2]
C0679006
UMLS CUI [1,3]
C0011008

Similar models

Dose Reduction

  1. StudyEvent: ODM
    1. Dose Reduction
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Dose Reduction Due to Adverse Experiences
C1707814 (UMLS CUI-1)
Dose Reduced, Decision, Date in time
Item
Date of decision to reduce the dose
date
C1707814 (UMLS CUI [1,1])
C0679006 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])

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