{"id":62822,"date":"2026-03-20T16:02:22","date_gmt":"2026-03-20T15:02:22","guid":{"rendered":"https:\/\/pharma-trend.com\/en\/incyte-to-highlight-late-breaking-hidradenitis-suppurativa-data-at-the-2026-american-academy-of-dermatology-aad-annual-meeting\/"},"modified":"2026-03-20T16:02:22","modified_gmt":"2026-03-20T15:02:22","slug":"incyte-to-highlight-late-breaking-hidradenitis-suppurativa-data-at-the-2026-american-academy-of-dermatology-aad-annual-meeting","status":"publish","type":"post","link":"https:\/\/pharma-trend.com\/en\/incyte-to-highlight-late-breaking-hidradenitis-suppurativa-data-at-the-2026-american-academy-of-dermatology-aad-annual-meeting\/","title":{"rendered":"Incyte to Highlight Late-Breaking Hidradenitis Suppurativa Data at the 2026 American Academy of Dermatology (AAD) Annual Meeting"},"content":{"rendered":"
\n

\n– New, late-breaking 54-week data for povorcitinib in hidradenitis suppurativa (STOP-HS1 & STOP-HS2) to be highlighted<\/i><\/p>\n

<\/a>
<\/a><\/p>\n

\n– Featured abstracts for ruxolitinib cream (Opzelura\u00ae<\/sup>) and povorcitinib include multiple ePosters in atopic dermatitis, hidradenitis suppurativa and vitiligo<\/i><\/p>\n

WILMINGTON, Del.–(BUSINESS WIRE)–$INCY<\/a> #AAD2026<\/a>–Incyte (Nasdaq:INCY) today announced that data from key programs in its Inflammation and Autoimmunity (IAI) franchise will be presented at the 2026 American Academy of Dermatology (AAD) Annual Meeting, to be held March 27 \u2013 31, 2026, in Denver.<\/p>\n

\n\u201cAt AAD 2026, we are presenting late\u2011breaking 54-week results from the Phase 3 STOP\u2011HS program evaluating povorcitinib in hidradenitis suppurativa (HS),\u201d said Jim Lee, M.D., Ph.D., Group Vice President, Inflammation and Autoimmunity, Incyte. \u201cThese data provide longer term evidence of the safety and efficacy of povorcitinib in HS patients and further strengthen the significant growth potential of our Inflammation and Autoimmunity franchise.\u201d<\/p>\n

\nDetails on key data presentations at AAD include:<\/p>\n

\nLate-Breaking Oral Presentations<\/span><\/b><\/p>\n

\nHidradenitis Suppurativa<\/i><\/b><\/p>\n

\nPovorcitinib in Patients With Moderate to Severe Hidradenitis Suppurativa: 54-Week Efficacy and Safety Results From the STOP-HS1 & STOP-HS2 Phase 3 Studies
\n
<\/b>(Session: S034 \u2013 Late-Breaking Research: Session 2. Saturday, March 28, 2026, 1:00 p.m. MT)<\/p>\n

\nePoster Exhibits<\/span><\/b><\/p>\n

\nAtopic Dermatitis<\/i><\/b><\/p>\n

\nRuxolitinib Cream Improves Patient-Reported Outcomes in Adults With Moderate Atopic Dermatitis (TRuE-AD4)
\n
<\/b>\u200b<\/b>(Abstract #: 75312)<\/p>\n

\nRuxolitinib Cream Is Efficacious in Adults With Moderate Atopic Dermatitis Regardless of Baseline Disease Severity and Previous Medication History
\n
<\/b>\u200b<\/b>(Abstract #: 70667)<\/p>\n

\nHidradenitis Suppurativa<\/i><\/b><\/p>\n

\nPovorcitinib for Moderate-to-Severe Hidradenitis Suppurativa: Week 24 Interim Phase 3 Results in Anti-TNF-Experienced Patients
\n
<\/b>(Abstract #: 75195)<\/p>\n

\nPhysician Perspectives on Diagnosis and Treatment of Hidradenitis Suppurativa: Results From the Global HERALD (Hidradenitis Suppurativa Experiences in the Real World) Survey
\n
<\/b>\u200b<\/b>(Abstract #: 75265)<\/p>\n

\nDisease Burden and Treatment History of Hidradenitis Suppurativa: Patient Perspectives From the Global HERALD (Hidradenitis Suppurativa Experiences in the Real World) Survey
\n
<\/b>\u200b<\/b>(Abstract #: 75268)<\/p>\n

\nVitiligo<\/i><\/b><\/p>\n

\nAssociation Between Repigmentation and Quality of Life Among Patients With Vitiligo Treated With Ruxolitinib Cream in the TRuE-V Studies
\n
<\/b>\u200b<\/b>(Abstract #: 75247)<\/p>\n

\nReal-World Factors Influencing Vitiligo Care: Insights From a Patient Survey Assessing the Use of Ruxolitinib Cream
\n
<\/b>\u200b<\/b>(Abstract #: 75258)<\/p>\n

\nMore information regarding the 2026 AAD Annual Meeting can be found at: https:\/\/www.aad.org\/member\/meetings-education\/am26\/education<\/a>.<\/p>\n

\nAbout Povorcitinib
\n
<\/b>Povorcitinib (INCB54707) is an oral small-molecule JAK1 selective inhibitor currently in Phase 3 clinical trials for HS, vitiligo and prurigo nodularis (PN), as well as a Phase 2 trial for asthma.<\/p>\n

\nAbout Opzelura\u00ae<\/sup> (ruxolitinib) Cream
\n
<\/b>Opzelura\u00ae <\/sup>(ruxolitinib) cream, a novel cream formulation of Incyte\u2019s selective JAK1\/JAK2 inhibitor ruxolitinib, approved by the U.S. FDA for the topical treatment of nonsegmental vitiligo in patients 12 years of age and older, is the first and only treatment for repigmentation approved for use in the United States. Opzelura is also approved in the U.S. for the topical short-term and non-continuous chronic treatment of mild to moderate AD in non-immunocompromised patients 2 years of age and older whose disease is not adequately controlled with topical prescription therapies, or when those therapies are not advisable. Use of Opzelura in combination with therapeutic biologics, other JAK inhibitors, or potent immunosuppressants, such as azathioprine or cyclosporine, is not recommended.<\/p>\n

\nIn Europe, Opzelura (ruxolitinib) cream 15mg\/g is approved for the treatment of non-segmental vitiligo with facial involvement in adults and adolescents from 12 years of age.<\/p>\n

\nIncyte has worldwide rights for the development and commercialization of Opzelura.<\/p>\n

\nOpzelura is a registered trademark of Incyte.<\/b><\/p>\n

\nAbout Incyte\u00ae
\n
<\/sup><\/b>Incyte is redefining what\u2019s possible in biopharmaceutical innovation. Through deep scientific expertise and a relentless focus on patients, we have built an established portfolio of first-in-class medicines and an extensive portfolio of next-generation medicines across our key franchises: Hematology, Oncology and Inflammation and Autoimmunity.<\/p>\n

\nTo learn more, visit Incyte.com<\/a> and Investor.Incyte.com<\/a>. Follow us on social media: LinkedIn<\/a>, X<\/a> and Instagram<\/a>.<\/p>\n

\nIncyte Forward-Looking Statements
\n
<\/b>Except for the historical information set forth herein, the matters set forth in this press release, including statements regarding the presentation of data from Incyte\u2019s clinical development pipeline and the potential for povorcitinib to provide a safe and effective treatment option for HS and further strengthen the significant growth potential of Incyte\u2019s Inflammation and Autoimmunity franchise, contain predictions, estimates and other forward-looking statements.<\/p>\n

\nThese forward-looking statements are based on Incyte\u2019s current expectations and subject to risks and uncertainties that may cause actual results to differ materially, including unanticipated developments in and risks related to: unanticipated delays; further research and development and the results of clinical trials possibly being unsuccessful or insufficient to meet applicable regulatory standards or warrant continued development; the ability to enroll sufficient numbers of subjects in clinical trials; determinations made by the FDA, EMA, and other regulatory authorities; the efficacy or safety of Incyte\u2019s products; the acceptance of Incyte\u2019s products in the marketplace; market competition; sales, marketing, manufacturing and distribution requirements; and other risks detailed from time to time in Incyte\u2019s reports filed with the U.S. Securities and Exchange Commission, including its annual report on form 10-K for the year ended December 31, 2025. Incyte disclaims any intent or obligation to update these forward-looking statements.<\/p>\n

Contacts<\/b> <\/p>\n

\nMedia<\/b>
media@incyte.com<\/a><\/p>\n

Investors<\/b>
ir@incyte.com<\/a><\/p>\n<\/div>\n","protected":false},"excerpt":{"rendered":"

– New, late-breaking 54-week data for povorcitinib in hidradenitis suppurativa (STOP-HS1 & STOP-HS2) to be highlighted – Featured abstracts for ruxolitinib cream (Opzelura\u00ae) and povorcitinib include multiple ePosters in atopic dermatitis, hidradenitis suppurativa and vitiligo WILMINGTON, Del.–(BUSINESS WIRE)–$INCY #AAD2026–Incyte (Nasdaq:INCY) today announced that data from key programs in its Inflammation and Autoimmunity (IAI) franchise will … [Read more…]<\/a><\/span><\/p>\n","protected":false},"author":4,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[13],"tags":[],"class_list":{"0":"entry","1":"post","2":"publish","3":"author-business","4":"post-62822","6":"format-standard","7":"category-industry"},"yoast_head":"\nIncyte to Highlight Late-Breaking Hidradenitis Suppurativa Data at the 2026 American Academy of Dermatology (AAD) Annual Meeting - Pharma Trend<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/pharma-trend.com\/en\/incyte-to-highlight-late-breaking-hidradenitis-suppurativa-data-at-the-2026-american-academy-of-dermatology-aad-annual-meeting\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Incyte to Highlight Late-Breaking Hidradenitis Suppurativa Data at the 2026 American Academy of Dermatology (AAD) Annual Meeting - Pharma Trend\" \/>\n<meta property=\"og:description\" content=\"– New, late-breaking 54-week data for povorcitinib in hidradenitis suppurativa (STOP-HS1 & STOP-HS2) to be highlighted – Featured abstracts for ruxolitinib cream (Opzelura\u00ae) and povorcitinib include multiple ePosters in atopic dermatitis, hidradenitis suppurativa and vitiligo WILMINGTON, Del.–(BUSINESS WIRE)–$INCY #AAD2026–Incyte (Nasdaq:INCY) today announced that data from key programs in its Inflammation and Autoimmunity (IAI) franchise will ... 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