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Review
. 2025 Sep;15(9):2361-2377.
doi: 10.1007/s13555-025-01487-y. Epub 2025 Jul 18.

Current Treatments and Future Directions for Hidradenitis Suppurativa: a Narrative Review of Completed and Ongoing Phase 3 Clinical Trials of Biologic Therapies

Affiliations
Review

Current Treatments and Future Directions for Hidradenitis Suppurativa: a Narrative Review of Completed and Ongoing Phase 3 Clinical Trials of Biologic Therapies

Amit Garg et al. Dermatol Ther (Heidelb). 2025 Sep.

Abstract

Hidradenitis suppurativa (HS) is a chronic, progressive inflammatory disease characterized by recurrent nodules, abscesses, draining tunnels, and scarring. Current treatment strategies for patients with HS typically involve a combination of therapeutic and surgical interventions that are tailored to the severity and extent of the disease. Treatment of patients with mild disease often includes topical or systemic antibiotics followed by anti-androgen therapies; however, these treatments are off-label and are generally only modestly effective for patients with moderate-to-severe disease. The lack of dedicated therapies targeting pathogenic mechanisms of HS has historically contributed to the unmet needs for disease management. These needs have been addressed recently by the emergence of biologic therapies, which can provide rapid and sustained symptom and disease control for patients who have poor treatment responses to initial therapies and progressive disease. Biologics have become an integral component in treatment strategies for patients with HS, but the unique clinical benefits and safety profile of each biologic can impact treatment decisions for individual patients. Recent elucidation of unique immunological pathways that contribute to HS pathophysiology may lead to the development of novel therapeutics that would expand the current therapeutic options, especially for patients with advanced disease. The purpose of this review is to provide an overview of the present therapeutic landscape for HS, with a particular focus on the mechanism of action, efficacy, and safety of biologic therapies either approved or under clinical investigation for the treatment of patients with HS. We also provide expert commentary on future directions of HS therapies as they pertain to recent research on the immunopathology of HS.

Keywords: Biologics; Efficacy; Hidradenitis suppurativa; Phase 3 clinical trials.

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Conflict of interest statement

Declarations. Conflict of interest: Amit Garg is an advisor for AbbVie, Almirall, Boehringer Ingelheim, Engitix, Immunitas Therapeutics, Incyte, Insmed, Novartis, Pfizer, Sonoma Biotherapeutics, Sun Pharma, UCB, Union Therapeutics, Zura Bio, and receives honoraria. He receives research grants from AbbVie, UCB, National Psoriasis Foundation, and CHORD COUSIN Collaboration (C3). He is co-copyright holder of HS-IGA and HiSQOL instruments. Jennifer Hsiao is an Editorial Board member of Dermatology and Therapy. Jennifer Hsiao was not involved in the selection of peer reviewers for the manuscript nor any subsequent editorial decisions. She is on the board of directors for the HS Foundation and has served as an advisor, investigator, and/or speaker for AbbVie, Aclaris, Amgen, AstraZeneca, Boehringer Ingelheim, Galderma, Incyte, Navigator Medicines, Novartis, Pfizer, Regeneron, Sanofi, UCB. Martina Porter is a consultant and/or investigator for AbbVie, Alumis, AnaptysBio, Aristea, Bayer, Eli Lilly, Incyte, Janssen, MoonLake, Novartis, Pfizer, Prometheus Laboratories, Regeneron, Trifecta Clinical (in conjunction with Acelyrin), Sonoma Bio, UCB, and ZuraBio. Vivian Shi is on the board of directors for the HS Foundation; serves as an advisor for the National Eczema Association; is a stock shareholder of Learn Health; and has served as an advisory board member, investigator, speaker, and/or received research funding from Sanofi Genzyme, Regeneron, AbbVie, Eli Lilly, Novartis, SUN Pharma, LEO Pharma, Pfizer, Incyte, Boehringer Ingelheim, Aristea Therapeutics, Menlo Therapeutics, Dermira, Burt’s Bees, Galderma, Kiniksa, UCB, Target-PharmaSolutions, Altus Lab/cQuell, MYOR, Polyfins Technology, GpSkin, and Skin Actives Scientific. Ethical approval: This article summarizes previously published clinical trial data and did not require approval or a waiver from an institutional review board. This article is based on previously conducted studies and does not contain any new studies with human participants or animals performed by any of the authors.

Figures

Fig. 1
Fig. 1
Molecular targets of therapies approved for treatmenta or under phase 3 investigation [–, , –86]. BTK Bruton’s tyrosine kinase, IL interleukin, JAK Janus kinase, Th T-helper, TNF tumor necrosis factor. aFDA-approved therapies. bIncludes biosimilars
Fig. 2
Fig. 2
Planned and ongoing phase 3 trials of investigational therapies grouped by mechanisms of action. BTK Bruton’s tyrosine kinase, dT draining fistula/tunnel, HiSCR Hidradenitis Suppurativa Clinical Response, IL interleukin, JAK Janus kinase

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