The objective of the study is to evaluate the effect, safety and tolerability of CDP323 in patients with relapsing forms of multiple sclerosis
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
232
The cumulative number of newly active lesions on standardized brain MRI scans after 24 weeks of treatment (Week 28).
The following lesions are considered newly active: new gadolinium enhancement on T1-weighted images; new lesions on T2-weighted images, but non-enhancing on T1-weighted images; new enlargement on T2-weighted images, but non-enhancing on T1-weighted images.
Time frame: Cumulative number of newly active lesions from baseline to Week 28.
Occurrence of any treatment emergent adverse event.
Time frame: During up to 24 weeks of treatment.
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Unnamed facility
Cullman, Alabama, United States
Unnamed facility
Phoenix, Arizona, United States
Unnamed facility
Tucson, Arizona, United States
Unnamed facility
Springs, Colorado, United States
Unnamed facility
Washington D.C., District of Columbia, United States
Unnamed facility
Maitland, Florida, United States
Unnamed facility
Atlanta, Georgia, United States
Unnamed facility
Northbrook, Illinois, United States
Unnamed facility
Fort Wayne, Indiana, United States
Unnamed facility
Kansas City, Kansas, United States
...and 61 more locations