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Incyte Reports Topline Data from P-III (STOP-HS1 & STOP-HS2) Trials of Povorcitinib (INCB054707) for Hidradenitis Suppurativa (HS)

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Incyte Reports Topline Data from P-III (STOP-HS1 & STOP-HS2) Trials of Povorcitinib (INCB054707) for Hidradenitis Suppurativa (HS)

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  • The 2 P-III (STOP-HS1 & STOP-HS2) trials assessed povorcitinib (45 or 75mg, QD, PO) vs PBO in mod. to sev. HS pts (≥18yrs.; n=600 each) for 12wks., followed by 42wk. extension & 30-day follow-up
  • STOP-HS1 met its 1EP, with povorcitinib (45 mg/75 mg) showing higher HiSCR50 rates at Wk. 12 (40.2%/40.6% vs 29.7%), while a biologics-experienced subgroup also showed higher response (34.2%/37.8% vs 21.9%), with >3-pt. Skin Pain NRS reductions (incl. NRS30), fewer flares, & rapid onset
  • STOP-HS2 also met its 1EP of superior HiSCR50 rates at Wk. 12 (42.3%/42.3% vs 28.6%), with higher response in mentioned subgroup (45.0%/40.0% vs 19.5%); data to support regulatory filings & presented at future meetings

Ref: Incyte  | Image: Incyte 

Related News:- Incyte Highlights P-III (TRuE-PN) Clinical Program Data of Opzelura (1.5% Ruxolitinib Cream) for Prurigo Nodularis (PN) at AAD 2025

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Ridhi Rastogi

Ridhi is an avid secondary researcher who follows trends in the biopharmaceutical and healthcare sectors to curate engaging content for the global audience. She works as a news editor at PharmaShots and loves to read books and explore new destinations.

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