This study will evaluate the efficacy and safety of different doses of EVO756 in adults with moderate to severe chronic spontaneous urticaria (CSU).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
182
Mean change from baseline in UAS7
Time frame: Week 12
Percent change from baseline in UAS7
Time frame: Week 12
Mean and percent change from baseline in UAS7
Time frame: Weeks 1, 2, 4, 8
Mean and percent change from baseline in ISS7
Time frame: Weeks 1, 2, 4, 8, 12
Mean and percent change from baseline in HSS7
Time frame: Weeks 1, 2, 4, 8, 12
Mean and percent change from baseline in AAS7
Time frame: Weeks 1, 2, 4, 8, 12
Proportion of subjects achieving UAS7 ≤ 6
Time frame: Weeks 1, 2, 4, 8, 12
Proportion of subjects achieving UAS7 = 0
Time frame: Weeks 1, 2, 4, 8, 12
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Placebo control
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NorthBay Clinical Research
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Integrated Research of Inland
Upland, California, United States
FOMAT Medical Research
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AMR Fort Myers
Fort Myers, Florida, United States
Advanced Clinical Research Institute
Tampa, Florida, United States
...and 43 more locations