The study is being conducted to evaluate the effect of 3 dosing regimens of povorcitinib on pulmonary function
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
247
Absolute change in pre-bronchodilator forced expiratory volume in the first 1 second (pre-BD FEV1)
To assess the effect of povorcitinib on lung function (pre-BD FEV1) between baseline and week 24
Time frame: Baseline ; Week 24
Number of asthma exacerbations during the Placebo Controlled (PC) period
Defined as a worsening of asthma
Time frame: Up to 28 weeks
Absolute change from baseline in pre-BD FEV1 at each visit
Time frame: Up to 14 months
Percent change from baseline in pre-BD FEV1 at each visit
Time frame: Up to 14 months
Absolute change from baseline in post-BD FEV1 at week 24
Time frame: Baseline; Week 24
Percent change from baseline in post-BD FEV1 at week 24
Time frame: Baseline; Week 24
Absolute change from baseline in pre-BD FVC at each visit
Time frame: Up to 14 months
Percent change from baseline in pre-BD FVC at each visit
Time frame: Up to 14 months
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...and 72 more locations