Multiple Sclerosis
Item
1. diagnosis of confirmed and documented ms defined by the revised mcdonald criteria.
boolean
C0026769 (UMLS CUI [1])
Multiple Sclerosis, Relapsing-Remitting
Item
2. subjects must be of the relapsing-remitting (r-r) type.
boolean
C0751967 (UMLS CUI [1])
Relapse Quantity | Gadolinium-Enhancing Lesion Quantity Magnetic Resonance Imaging
Item
3. subject has experienced prior to screening at least one documented relapse in 12 months or at least 2 documented relapses in the 24 months or one documented relapse between 12 - 24 months with at least 1 documented t1-gd enhancing lesion in the mri performed 12 months prior screening.
boolean
C0035020 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C1333400 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
C0024485 (UMLS CUI [2,3])
disease length
Item
4. disease duration for at least 6 months.
boolean
C0872146 (UMLS CUI [1])
Ambulatory Kurtzke multiple sclerosis rating scale
Item
5. ambulatory with converted kurtzke edss score of 0 - 5.
boolean
C0439841 (UMLS CUI [1,1])
C0451246 (UMLS CUI [1,2])
Condition Neurologic Stable | Relapse Free of
Item
6. relapse free and stable neurological condition at least for 30 days prior screening.
boolean
C0348080 (UMLS CUI [1,1])
C0205494 (UMLS CUI [1,2])
C0205360 (UMLS CUI [1,3])
C0035020 (UMLS CUI [2,1])
C0332296 (UMLS CUI [2,2])
Age
Item
7. age - 18-55 (inclusive)
boolean
C0001779 (UMLS CUI [1])
Copaxone | glatiramer acetate
Item
1. previous use of copaxone (glatiramer acetate)
boolean
C0528175 (UMLS CUI [1])
C0289884 (UMLS CUI [2])
Adrenal Cortex Hormones
Item
2. treatment with corticosteroids within 30 days prior screening or between screening and baseline.
boolean
C0001617 (UMLS CUI [1])
Adrenal Cortex Hormones chronic
Item
3. chronic corticosteroids treatment - more than 30 consecutive days.
boolean
C0001617 (UMLS CUI [1,1])
C0205191 (UMLS CUI [1,2])
Medical condition Clinical Significance | Medical condition Unstable
Item
4. subject with any clinically significant or unstable medical condition.
boolean
C3843040 (UMLS CUI [1,1])
C2826293 (UMLS CUI [1,2])
C3843040 (UMLS CUI [2,1])
C0443343 (UMLS CUI [2,2])
Study Subject Participation Status
Item
5. subjects participating in any other clinical trial (within 12 weeks prior to screening and thereafter).
boolean
C2348568 (UMLS CUI [1])
Hypersensitivity Gadolinium | Magnetic Resonance Imaging Receive Unable
Item
6. known history of sensitivity to gadolinium and inability to successfully undergo mri scanning.
boolean
C0020517 (UMLS CUI [1,1])
C0016911 (UMLS CUI [1,2])
C0024485 (UMLS CUI [2,1])
C1514756 (UMLS CUI [2,2])
C1299582 (UMLS CUI [2,3])