ID

15581

Description

Principal Investigator: Luisa Klotz Collaborator: Novartis Information provided by (Responsible Party):University Hospital Muenster -Study to Assess Immune Function and MRI Disease Activity in RRMS Patients When Switching From Natalizumab to Gilenya (ToFingo2) Purpose A trial in patients with relapsing remitting multiple sclerosis (RRMS) Main objectives: •To evaluate changes in the reconstitution of immune surveillance over time upon switching from natalizumab to fingolimod assessed by a change in the expression of CD49d. •To evaluate changes in the migratory capacity of immune cells/peripheral blood mononuclear cells (PBMCs) upon switching from natalizumab to fingolimod in an in-vitro model of the blood-brain-barrier (BBB). •To evaluate changes in paraclinical disease activity over time upon switching from natalizumab to fingolimod assessed by MRI (changes in Gd+, T2w lesions and DTI). •To evaluate changes in T1w / FLAIR lesions upon switching from natalizumab to fingolimod. For further Information please visit https://clinicaltrials.gov/ct2/show/NCT02325440

Lien

https://clinicaltrials.gov/ct2/show/NCT02325440

Mots-clés

  1. 03/06/2016 03/06/2016 -
Téléchargé le

3 juin 2016

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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ToFingo Screening V1 Study relevant assessments NCT02325440

ToFingo Screening V1 Study relevant assessments NCT02325440

Study relevant assessments
Description

Study relevant assessments

Alias
UMLS CUI-1
C3472195
Pregnancy test; Serum
Description

Pregnancy test; Serum

Type de données

float

Unités de mesure
  • U/L
Alias
UMLS CUI [1]
C1880076
U/L
Peripheral blood taken
Description

Peripheral blood taken

Type de données

boolean

Alias
UMLS CUI [1]
C0005834
Date of collection
Description

Date of collection

Type de données

date

Alias
UMLS CUI [1,1]
C0005834
UMLS CUI [1,2]
C1317250

Similar models

ToFingo Screening V1 Study relevant assessments NCT02325440

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Study relevant assessments
C3472195 (UMLS CUI-1)
Pregnancy test; Serum
Item
Pregnancy test; Serum
float
C1880076 (UMLS CUI [1])
Peripheral blood taken
Item
Peripheral blood taken
boolean
C0005834 (UMLS CUI [1])
Date of collection
Item
Date of collection
date
C0005834 (UMLS CUI [1,1])
C1317250 (UMLS CUI [1,2])

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