The purpose of this study is to evaluate the maximal use of ruxolitinib cream in adult and adolescent participants with hidradenitis suppurativa.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
24
Ruxolitinib cream applied topically to the affected area as a thin film twice daily.
Number of participants with Treatment-emergent Adverse Events (TEAEs)
Defined as adverse events reported for the first time or worsening of a pre-existing event after the first application of study drug.
Time frame: Up to 24 weeks
Number of participants with TEAEs leading to treatment interruption, discontinuation
Number of participants with TEAEs leading to dose interruption or discontinuation
Time frame: Up to 24 weeks
Pharmacokinetics Parameter (PK): Cmax of INCB018424
Defined as maximum observed plasma concentration of INCB018424.
Time frame: Up to 24 weeks
Pharmacokinetics Parameter: Tmax of INCB018424
Defined as the time to reach the maximum plasma concentration of INCB018424.
Time frame: Up to 24 weeks
Pharmacokinetics Parameter: AUC 0-12 of INCB018424
Defined as the area under the plasma or serum concentration-time curve from Hour 0 to 12 hours of INCB018424.
Time frame: Up to 24 weeks
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