Hereditary Angioedema Market Overview
Valued at nearly USD 3 billion in 2023, the Hereditary Angioedema market is projected to witness substantial growth, primarily fueled by the launch of innovative therapies. HAE is a rare inherited disorder marked by repeated episodes of severe swelling affecting areas such as the face, extremities, gastrointestinal tract, and airway.
Existing treatment options include C1 esterase inhibitor (C1-INH) therapies like BERINERT and RUCONEST, kallikrein inhibitors such as Ecallantide, bradykinin receptor antagonists like FIRAZYR, and prophylactic agents including CINRYZE, HAEGARDA, and LANADELUMAB. The United States dominates the global market, contributing nearly 90% of total revenue. Approximately 65% of patients diagnosed with HAE are women.
The pipeline remains highly promising, featuring candidates such as Navenibart (STAR-0215), Donidalorsen, NTLA-2002, and Sebetralstat. Major 2024 developments include FDA acceptance of Ionis’s NDA for Donidalorsen, KalVista’s NDA filing for Sebetralstat, and Astria’s partnership with Ypsomed for STAR-0215. Positive Phase III OASIS-HAE data for Donidalorsen demonstrated more than a 90% reduction in attack rates, reinforcing strong future market growth potential.
DelveInsight’s report, “Hereditary Angioedema Market Insights, Epidemiology, and Market Forecast – 2034,” delivers an extensive assessment of HAE, covering both historical and forecasted epidemiology as well as market dynamics across the United States, EU4 (Germany, Spain, Italy, France), the UK, and Japan. The report evaluates current therapies, pipeline assets, drug-wise market share, and overall market size from 2020 to 2034. It further examines treatment pathways, growth drivers, barriers, and unmet needs to identify key opportunities and future expansion trends.
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Key Highlights from the Hereditary Angioedema Market Report
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Hereditary Angioedema Overview
HAE is a rare inherited disorder characterized by episodic, potentially life-threatening swelling of the skin and mucosal tissues, particularly affecting the face, limbs, gastrointestinal tract, and airway. The condition arises due to C1-INH deficiency or dysfunction, resulting in excessive bradykinin production and increased vascular permeability. HAE is categorized into Type I, Type II, and normal C1-INH variants.
Women are disproportionately affected, and triggers such as stress, trauma, or hormonal fluctuations may precipitate attacks. Available treatments include acute therapies (C1-INH products, kallikrein inhibitors, bradykinin antagonists) and preventive options such as lanadelumab and HAEGARDA. Emerging innovations, including RNA-based, monoclonal antibody, and gene-editing therapies, aim to deliver longer-lasting and more convenient disease control. However, challenges remain in ensuring global access and achieving curative outcomes.
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Hereditary Angioedema Epidemiology Insights
In 2023, the U.S. recorded nearly 7,000 diagnosed HAE cases, with Type I representing the majority (~5,500 cases). Approximately 1,000 cases were observed among individuals aged 17–65 years.
The epidemiological analysis (2020–2034) segments the disease by total prevalence, severity, gender distribution, and episodic versus chronic cases across the 7MM.
Hereditary Angioedema Epidemiology Segmentation:
The Hereditary Angioedema market report proffers epidemiological analysis for the study period 2020-2034 in the 7MM segmented into:
Hereditary Angioedema Pipeline and Drug Uptake
Navenibart (Astria Therapeutics):
Navenibart (STAR-0215) by Astria Therapeutics is a long-acting monoclonal antibody targeting plasma kallikrein, developed to provide sustained prevention of HAE attacks with dosing every three or six months. Results from the ALPHA-STAR Phase Ib/II trial showed a 90–96% reduction in attack frequency and strong safety and tolerability. Following these promising results, Astria plans to begin Phase III trials in Q1 2025, with top-line data expected by late 2026.
Donidalorsen (Ionis Pharmaceuticals):
Donidalorsen (IONIS-PKK-LRx) by Ionis Pharmaceuticals is an investigational ligand-conjugated antisense (LICA) therapy designed to inhibit the production of prekallikrein (PKK), a key mediator in Hereditary Angioedema (HAE) attacks. By lowering PKK levels, it aims to prevent acute episodes effectively. In the Phase III OASIS-HAE trial, subcutaneous donidalorsen administered every 4 weeks reduced the mean monthly attack rate by 81% versus placebo, while dosing every 8 weeks achieved a 55% reduction.
Hereditary Angioedema Therapies and Key Companies
Discover more about therapies set to grab major Hereditary Angioedema market share @ Hereditary Angioedema Medication and Companies
Hereditary Angioedema Market Dynamics
Hereditary Angioedema Market Drivers
Hereditary Angioedema Market Barriers
Scope of the Hereditary Angioedema Market Report
To know more about Hereditary Angioedema companies working in the treatment market, visit @ Hereditary Angioedema Clinical Trials and Therapeutic Assessment
Table of Contents
1. Hereditary Angioedema Market Report Introduction
2. Executive Summary for Hereditary Angioedema
3. SWOT analysis of Hereditary Angioedema
4. Hereditary Angioedema Patient Share (%) Overview at a Glance
5. Hereditary Angioedema Market Overview at a Glance
6. Hereditary Angioedema Disease Background and Overview
7. Hereditary Angioedema Epidemiology and Patient Population
8. Country-Specific Patient Population of Hereditary Angioedema
9. Hereditary Angioedema Current Treatment and Medical Practices
10. Hereditary Angioedema Unmet Needs
11. Hereditary Angioedema Emerging Therapies
12. Hereditary Angioedema Market Outlook
13. Country-Wise Hereditary Angioedema Market Analysis (2020-2034)
14. Hereditary Angioedema Market Access and Reimbursement of Therapies
15. Hereditary Angioedema Market Drivers
16. Hereditary Angioedema Market Barriers
17. Hereditary Angioedema Appendix
18. Hereditary Angioedema Report Methodology
19. DelveInsight Capabilities
20. Disclaimer
21. About DelveInsight
About DelveInsight
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