This is a 12-week study to assess the safety, tolerability, pharmacokinetics and pharmacodynamics of oral CS-0777 in patients with Multiple Sclerosis.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
25
0.1 mg, once-weekly, for 12 weeks
0.3 mg, once-weekly or once every 2 weeks, for 12 weeks
0.6 mg, once-weekly or once every 2 weeks, for 12 weeks
Unnamed facility
Denver, Colorado, United States
Unnamed facility
Port Orange, Florida, United States
Unnamed facility
Lenexa, Kansas, United States
Unnamed facility
Billings, Montana, United States
Unnamed facility
Philadelphia, Pennsylvania, United States
Safety and tolerability.
Time frame: 12 weeks, with 4 weeks to follow-up
Pharmacodynamic response (lymphocyte counts Pharmacokinetics Exploratory efficacy based on brain MRI lesions)
Time frame: 12 weeks, with 4 weeks to follow up.
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