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Incyte (INCY) Announces 52-Week Results from Phase 2 Study Evaluating Povorcitinib in Patients with HS

Incyte (INCY) Announces 52-Week Results from Phase 2 Study Evaluating Povorcitinib in Patients with HS
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Kurt brownHidradenitis suppurativaJoslyn kirbyConference of the european hidradenitis suppurativa foundationInternational hidradenitis suppurativa severity score systemGlobal program headDrug developmentDepartment of dermatology at penn state healthWall streetEuropean hidradenitis suppurativa foundationInflammatory noduleAssociate vice presidentAssociate professorVice chairPenn state

Incyte Announces 52-Week Results from Phase 2 Study Evaluating Povorcitinib (INCB54707) in Patients with Hidradenitis Suppurativa

Results from open-label extension period of the Phase 2 trial demonstrate that longer-term treatment with povorcitinib 75 mg resulted in sustained and durable efficacy across all treatment arms Data

United statesCatalina lovemanKurt brownChristine chiouHidradenitis suppurativaJoslyn kirbyEuropean academy of dermatologyNational centerInternational hidradenitis suppurativa severity score systemRare diseases information centerDrug developmentExchange commissionConference of the european hidradenitis suppurativa foundationEuropean hidradenitis suppurativa foundationGlobal program headDepartment of dermatology at penn state health