Eligibility Relapsing Remitting Multiple Sclerosis NCT01963611

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
male or female, between the ages of 18 and 60 years
Descripción

ID.1

Tipo de datos

boolean

subject is able to learn and self-administer subcutaneous injections (a care-giver may be trained to inject the subject)
Descripción

ID.2

Tipo de datos

boolean

subjects must have a current diagnosis of relapsing remitting multiple sclerosis (rrms) (according to the 2010 mcdonald ms diagnostic criteria)
Descripción

ID.3

Tipo de datos

boolean

other protocol defined inclusion criteria could apply
Descripción

ID.4

Tipo de datos

boolean

Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
any multiple sclerosis categorized as primary progressive, secondary progressive or progressive relapsing
Descripción

ID.5

Tipo de datos

boolean

allergy to mannitol, plovamer acetate, copaxone (glatiramer acetate), gd contrast for mri
Descripción

ID.6

Tipo de datos

boolean

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)
Descripción

ID.7

Tipo de datos

boolean

contraindication to copaxone use
Descripción

ID.8

Tipo de datos

boolean

other protocol defined exclusion criteria could apply
Descripción

ID.9

Tipo de datos

boolean

Similar models

Eligibility Relapsing Remitting Multiple Sclerosis NCT01963611

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
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
Item Group
C0680251 (UMLS CUI)
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