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Informatie:
Fout:
ID
34549
Beschrijving
Efficacy, Safety, and Tolerability of Plovamer Acetate (Pathway 1); ODM derived from: https://clinicaltrials.gov/show/NCT01963611
Link
https://clinicaltrials.gov/show/NCT01963611
Trefwoorden
Versies (2)
- 19-01-19 19-01-19 -
- 06-02-20 06-02-20 - Christian Arras
Houder van rechten
see on clinicaltrials.gov
Geüploaded op
19 januari 2019
DOI
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Licentie
Creative Commons BY-NC 3.0
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Eligibility Relapsing Remitting Multiple Sclerosis NCT01963611
Eligibility Relapsing Remitting Multiple Sclerosis NCT01963611
- StudyEvent: Eligibility
Similar models
Eligibility Relapsing Remitting Multiple Sclerosis NCT01963611
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
ID.1
Item
male or female, between the ages of 18 and 60 years
boolean
ID.2
Item
subject is able to learn and self-administer subcutaneous injections (a care-giver may be trained to inject the subject)
boolean
ID.3
Item
subjects must have a current diagnosis of relapsing remitting multiple sclerosis (rrms) (according to the 2010 mcdonald ms diagnostic criteria)
boolean
ID.4
Item
other protocol defined inclusion criteria could apply
boolean
ID.5
Item
any multiple sclerosis categorized as primary progressive, secondary progressive or progressive relapsing
boolean
ID.6
Item
allergy to mannitol, plovamer acetate, copaxone (glatiramer acetate), gd contrast for mri
boolean
ID.7
Item
any requirement for continuous systemic glucocorticoid administration during the trial period. (note: treatment with interferons such as avonex®, rebif®, or betaseron® will be allowed until the baseline visit, as no wash-out period is needed)
boolean
ID.8
Item
contraindication to copaxone use
boolean
ID.9
Item
other protocol defined exclusion criteria could apply
boolean