The purpose of this study is to determine the safety and tolerability of the MDX-1100 regimen in subjects with active Ulcerative colitis(UC) and determine the response rate at day 57 in patients administered MDX-1100.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
110
10mg/kg/dose sterile saline injected every other week for a total of 4 doses
10mg/kg/dose MDX-1100 injected every other week for a total of 4 doses
Change in Mayo score at Day 57 compared with Screening
Time frame: Day 57
the remission rate
Time frame: Day 57
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Advanced Medical Research Center
Port Orange, Florida, United States
Florida Medical Clinic-Tampa Clinic
Tampa, Florida, United States
Northwestern University Feinberg School of Medicine
Chicago, Illinois, United States
Chevy Chase Clinical Research
Chevy Chase, Maryland, United States
Washington University School of Medicine
St Louis, Missouri, United States
Mount Sinai School of Medicine
New York, New York, United States
Dayton Science Institute
Dayton, Ohio, United States
Unnamed facility
Abbotsford, British Columbia, Canada
Unnamed facility
Vancouver, British Columbia, Canada
Unnamed facility
Toronto, Ontario, Canada
...and 34 more locations