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Report Overview

Hidradenitis suppurativa (HS) is a chronic, painful skin condition characterized by inflamed nodules, abscesses, and scarring, primarily in areas with sweat glands. According to Kimberly Ballard et al., 2024, the disease accounts for around 1% to 4% of the global population. The drug pipeline for HS includes promising biologics such as Bimekizumab, targeting key inflammatory pathways. According to the hidradenitis suppurativa pipeline analysis by Expert Market Research, there is a growing focus on developing novel immunomodulatory therapies and precision medicine for the condition. Rising awareness, improved diagnosis, and ongoing clinical trials are expected to drive significant market growth in the coming years.

  • Major companies involved in the hidradenitis suppurativa pipeline analysis include Avalo Therapeutics, Inc., Citryll BV, and others.

  • Leading drugs currently in the pipeline include AVTX-009, CIT-013, SBT777101, and others.

  • The hidradenitis suppurativa drug pipeline is expanding due to increasing R&D in biologics, rising clinical trials for IL-17 inhibitors, and growing FDA designations for novel therapies.

Report Coverage

The Hidradenitis Suppurativa Pipeline Analysis Report by Expert Market Research gives comprehensive insights into hidradenitis suppurativa therapeutics currently undergoing clinical trials. It covers various aspects related to the details of each of these drugs under development for hidradenitis suppurativa. The hidradenitis suppurativa report assessment includes the analysis of over 100 pipeline drugs and 50+ companies. The hidradenitis suppurativa pipeline landscape will include an analysis based on efficacy and safety measure outcomes published for the trials, including their adverse effects on patients suffering from the condition, and alignment with hidradenitis suppurativa treatment guidelines to ensure optimal care practices.

The assessment part will include a detailed analysis of each drug, drug class, clinical studies, phase type, drug type, route of administration, and ongoing product development activities related to hidradenitis suppurativa.

Hidradenitis Suppurativa Pipeline Analysis By Drug Class

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Hidradenitis Suppurativa Pipeline Outlook

Hidradenitis suppurativa (HS) is a chronic, inflammatory skin condition characterized by painful, boil-like lumps, typically forming in areas where skin rubs together, such as the armpits, groin, and under the breasts. It occurs due to follicular occlusion, inflammation, and immune system dysregulation, often resulting in abscesses, tunnels under the skin, and scarring over time.

Hidradenitis suppurativa is treated through antibiotics, corticosteroids, hormonal therapy, immunosuppressants, and biologics to reduce inflammation, manage symptoms, and prevent flare-ups, with treatment tailored to disease severity and progression. In October 2023, the United States Food and Drug Administration approved Novartis’ Cosentyx® (secukinumab) as the first IL-17A inhibitor for moderate to severe hidradenitis suppurativa, demonstrating early and sustained symptom relief in pivotal Phase III trials.

Hidradenitis Suppurativa Epidemiology

According to Kimberly Ballard et al., 2024, the estimated prevalence of hidradenitis suppurativa ranges from 1%-4%, with figures likely underestimated due to underreporting and misdiagnosis. As per Verma, Kritin K et al., 2024, a large-scale study involving 407,333 individuals reported a prevalence of 0.40%, with a female-to-male ratio of 4:1. The highest prevalence was observed in individuals aged 18–25 years and among Black patients at 0.76%.

Hidradenitis Suppurativa – Pipeline Therapeutic Assessment

This section of the report covers the analysis of hidradenitis suppurativa drug candidates based on several segmentations, including:

By Phase

  • Late-Stage Products (Phase 3 and Phase 4)
  • Mid-Stage Products (Phase 2)
  • Early-Stage Products (Phase I)
  • Preclinical and Discovery Stage Products

By Drug Class

  • Small Molecules
  • Gene Therapies
  • Monoclonal Antibodies
  • Peptides
  • Polymers

By Route of Administration

  • Oral
  • Parenteral
  • Others

Hidradenitis Suppurativa Pipeline Assessment Segmentation, By Phases

The report covers phase I, phase II, phase III, phase IV, and early-phase drugs. The coverage includes an in-depth analysis of each drug across these phases. According to EMR analysis, phase II (at 37%), covers a major share of the total hidradenitis suppurativa clinical trials. It is followed closely by phase III with 37%. Phase I accounts for 16%. The strong presence in advanced stages reflects growing research interest, which is expected to positively impact the hidradenitis suppurativa treatment landscape through improved treatment outcomes and drug availability.

Hidradenitis Suppurativa Pipeline Assessment Segmentation, By Drug Classes

The drug molecule categories covered under the hidradenitis suppurativa pipeline analysis include small molecules, gene therapies, monoclonal antibodies, peptides, and polymers. The hidradenitis suppurativa report provides a comparative analysis of the drug classes for each drug in various phases of clinical trials for hidradenitis suppurativa. Interleukin inhibitors are emerging as a promising drug class in the hidradenitis suppurativa treatment pipeline. For instance, lutikizumab, a dual-variable-domain interleukin-1α/1β antagonist, demonstrated higher HiSCR 50 response rates in a Phase 2 trial. It is now advancing to Phase 3, targeting inflammatory pathways linked to moderate to severe hidradenitis suppurativa in patients unresponsive to anti-TNF therapies.

Hidradenitis Suppurativa Clinical Trials – Key Players

The EMR report for the hidradenitis suppurativa pipeline covers the profile of key companies involved in clinical trials and their drugs under development. It provides a hidradenitis suppurativa therapeutic assessment, analyzing the competitive dynamics of the clinical trial landscape. Below is the list of a few players involved in hidradenitis suppurativa clinical trials:

  • Avalo Therapeutics, Inc.
  • Citryll BV
  • Huaota Biopharmaceutical Co., Ltd.
  • Sonoma Biotherapeutics, Inc.
  • Leadingtac Pharmaceutical (Shaoxing) Co., Ltd.
  • Novartis Pharmaceuticals
  • Incyte Corporation
  • Merck Sharp & Dohme LLC
  • Eli Lilly and Company
  • AbbVie
  • Sanofi

Hidradenitis Suppurativa – Emerging Drugs Profile

This section covers the detailed analysis of each drug under multiple phases, including phase I, phase II, phase III, phase IV, and emerging drugs for hidradenitis suppurativa. It includes product description, trial ID, study type, drug class, mode of administration, and recruitment status of hidradenitis suppurativa drug candidates.

Drug: AVTX-009

AVTX-009 is a humanized monoclonal antibody targeting interleukin-1 beta, that neutralizes the inflammatory activity in moderate to severe hidradenitis suppurativa. Sponsored by Avalo Therapeutics, Inc., the Phase 2 LOTUS study is evaluating the drug’s efficacy and safety compared to placebo. Researchers are assessing how AVTX-009 is reducing HS symptoms over a 16-week treatment period, with patients receiving one of two dosage regimens or placebo.

Drug: CIT-013

CIT-013, sponsored by Citryll BV, is currently being evaluated in a Phase 2a trial for hidradenitis suppurativa (HS). This study aims to determine whether CIT-013 can reduce the disease activity and assess its safety profile. CIT-013 is a first-in-class monoclonal antibody designed to prevent and clear extracellular traps, such as NETs and EETs, which are linked to chronic inflammation in HS and other immune-mediated disorders.

Biological: SBT777101

SBT777101, sponsored by Sonoma Biotherapeutics, Inc., is currently undergoing a Phase 1 clinical trial to assess its safety, tolerability, pharmacokinetics, and pharmacodynamics in patients with hidradenitis suppurativa. This study is examining the effects of single ascending doses of SBT777101, an autologous CAR-Treg cell therapy designed to target inflamed tissue. The objective is to reduce inflammation and restore immune balance using next-generation genome-edited regulatory T cells.

*Please note that this is only a partial list; the complete list of drugs will be available in the full report.*

Key Questions Answered in the Hidradenitis Suppurativa Pipeline Insight Report

  • Which companies/institutions are leading the hidradenitis suppurativa drug development?
  • What is the efficacy and safety profile of hidradenitis suppurativa pipeline drugs?
  • Which company is leading the hidradenitis suppurativa pipeline development activities?
  • What is the current hidradenitis suppurativa commercial assessment?
  • What are the opportunities and challenges present in the hidradenitis suppurativa pipeline landscape?
  • Which company is conducting major trials for hidradenitis suppurativa drugs?
  • Which companies/institutions are involved in hidradenitis suppurativa collaborations aimed at providing enhanced therapeutic alternatives for patients?
  • What are the geographies covered for clinical trials in hidradenitis suppurativa?

Reasons To Buy This Report

The Hidradenitis Suppurativa Pipeline Analysis Report provides a strategic overview of the latest and future landscape of treatments for hidradenitis suppurativa. It provides necessary information for making informed investment decisions along with research, development, and strategic planning efforts. The stakeholders will benefit from the essential insights into hidradenitis suppurativa collaborations, regulatory environments, and potential growth opportunities.

Related Reports

Global Clinical Trials Market

Hidradenitis Suppurativa Treatment Market

Hidradenitis Suppurativa Epidemiology Forecast

*While we strive to always give you current and accurate information, the numbers depicted on the website are indicative and may differ from the actual numbers in the main report. At Expert Market Research, we aim to bring you the latest insights and trends in the market. Using our analyses and forecasts, stakeholders can understand the market dynamics, navigate challenges, and capitalize on opportunities to make data-driven strategic decisions.*

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Report Summary

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Please note that the figures mentioned in the description serve as estimates and may vary from the actual figures presented in the final report.

Scope of the Report

Details

Drug Pipeline by Clinical Trial Phase

  • Late-Stage Products (Phase III and Phase IV)
  • Mid-Stage Products (Phase II)
  • Early-Stage Products (Phase I)
  • Preclinical and Discovery Stage Products

Route of Administration

  • Oral
  • Parenteral
  • Others

Drug Classes

  • Small Molecules
  • Gene Therapies
  • Monoclonal Antibodies
  • Peptides
  • Polymers

Leading Sponsors Covered

  • Avalo Therapeutics, Inc.
  • Citryll BV
  • Huaota Biopharmaceutical Co., Ltd.
  • Sonoma Biotherapeutics, Inc.
  • Leadingtac Pharmaceutical (Shaoxing) Co., Ltd.
  • Novartis Pharmaceuticals
  • Incyte Corporation
  • Merck Sharp & Dohme LLC
  • Eli Lilly and Company
  • AbbVie
  • Sanofi

Geographies Covered

  • North America
  • Europe
  • Asia Pacific
  • Others

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