24
Participants
Start Date
May 7, 2024
Primary Completion Date
June 7, 2024
Study Completion Date
June 7, 2024
Povorcitinib
Povorcitinib will be administered at protocol defined dose.
Levonorgestrel/Ethinyl estradiol
Levonorgestrel/Ethinyl estradiol will be administered at protocol defined dose.
Celerion Clinical Research Unit, Tempe
Lead Sponsor
Incyte Corporation
INDUSTRY