유전성 혈관부종 치료제 시장 - 세계 산업 규모, 점유율, 동향, 기회, 예측, 약제 클래스별, 유통 채널별, 용도별, 지역별 부문, 경쟁(2020-2030년)
Hereditary Angioedema Therapeutics Market - Global Industry Size, Share, Trends, Opportunity, and Forecast, Segmented By Drug Class, By Distribution Channel, By Application, By Region and Competition, 2020-2030F
상품코드 : 1691775
리서치사 : TechSci Research
발행일 : 2025년 03월
페이지 정보 : 영문 183 Pages
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한글목차

유전성 혈관부종 치료제 세계 시장 규모는 2024년에 43억 6,000만 달러로 평가되었고, 예측 기간 동안 72억 8,000만 달러에 달할 것으로 예상되며, 2030년까지 8.89%의 연평균 복합 성장률(CAGR)을 나타낼 것으로 예상됩니다.

세계 유전성 혈관부종 치료제 시장은 인지도 향상, 진단 능력 향상, 새로운 치료 옵션의 도입으로 인해 크게 성장하고 있습니다. 유전학 연구의 발전으로 조기에 정확한 진단이 가능해져 적시에 개입하고 질병을 더 잘 관리할 수 있게 되었습니다. 제약회사들은 단클론 항체 및 저분자 억제제를 포함한 표적 치료제 개발에 집중하여 장기적인 예방 및 급성기 치료 솔루션을 제공합니다. 유전성 혈관성 부종의 유병률 증가는 의료비 지출 증가 및 환자 지원 활동과 함께 시장 성장을 더욱 촉진하고 있습니다. 또한, 혁신적인 치료법에 대한 규제 당국의 승인과 피하 및 경구 치료 옵션의 출현은 환자의 복약 순응도와 편의성을 향상시켜 업계에 좋은 전망을 가져다주고 있습니다.

시장 개요
예측 기간 2026-2030년
시장 규모 : 2024년 43억 6,000만 달러
시장 규모 : 2030년 72억 8,000만 달러
CAGR : 2025-2030년 8.89%
급성장 부문 예방약
최대 시장 북미

강력한 신약 파이프라인과 R&D 투자 증가가 경쟁 구도를 형성하고 있습니다. 바이오 제약사들은 효능을 개선하고 부작용을 줄이며 투여 방법을 개선하는 차세대 치료법을 모색하고 있습니다. 정맥주사에서 피하주사 및 경구투여로의 전환은 표준 치료법을 변화시켜 환자와 의료진의 부담을 줄여주고 있습니다. 제약사, 연구기관, 환자 단체 간의 공동연구와 전략적 파트너십을 통해 의약품 개발이 가속화되고 있습니다. 급성기 치료에만 의존하지 않고 예방적 조치를 원하는 환자가 증가함에 따라 예방적 치료의 확대는 시장의 장기적인 지속성을 촉진할 것으로 예상됩니다.

주요 시장 성장 촉진요인

연구개발(R&D) 진행 상황

주요 시장 이슈

높은 치료비

주요 시장 동향

개인 맞춤형 의료 접근법

목차

제1장 개요

제2장 조사 방법

제3장 주요 요약

제4장 세계의 유전성 혈관부종 치료제 시장 전망

제5장 아시아태평양의 유전성 혈관부종 치료제 시장 전망

제6장 유럽의 유전성 혈관부종 치료제 시장 전망

제7장 북미의 유전성 혈관부종 치료제 시장 전망

제8장 남미의 유전성 혈관부종 치료제 시장 전망

제9장 중동 및 아프리카의 유전성 혈관부종 치료제 시장 전망

제10장 시장 역학

제11장 시장 동향과 발전

제12장 세계의 유전성 혈관부종 치료제 시장 : SWOT 분석

제13장 Porter의 Five Forces 분석

제14장 경쟁 구도

제15장 전략적 제안

제16장 리서치사에 대해 & 면책사항

LSH
영문 목차

영문목차

Global Hereditary Angioedema Therapeutics Market was valued at USD 4.36 Billion in 2024 and is expected to reach USD 7.28 Billion in the forecast period with a CAGR of 8.89% through 2030. The global hereditary angioedema therapeutics market is experiencing significant expansion, driven by increasing awareness, improved diagnostic capabilities, and the introduction of novel treatment options. Advances in genetic research have enabled early and accurate diagnosis, allowing for timely intervention and better disease management. Pharmaceutical companies are focusing on developing targeted therapies, including monoclonal antibodies and small-molecule inhibitors, to provide long-term prophylaxis and acute treatment solutions. The growing prevalence of hereditary angioedema, coupled with rising healthcare expenditure and patient advocacy efforts, is further supporting market growth. Furthermore, regulatory approvals for innovative therapies and the emergence of subcutaneous and oral treatment options are enhancing patient adherence and convenience, creating a favorable outlook for the industry.

Market Overview
Forecast Period2026-2030
Market Size 2024USD 4.36 Billion
Market Size 2030USD 7.28 Billion
CAGR 2025-20308.89%
Fastest Growing SegmentProphylaxis
Largest MarketNorth America

A strong pipeline of novel drugs and increased investment in research and development are shaping the competitive landscape. Biopharmaceutical companies are exploring next-generation therapies that offer enhanced efficacy, fewer side effects, and improved administration methods. The shift from intravenous to subcutaneous and oral treatments is transforming the standard of care, reducing the burden on patients and healthcare providers. Collaborations and strategic partnerships between pharmaceutical firms, research institutions, and patient organizations are accelerating drug development and market penetration. The expansion of prophylactic treatments is expected to drive long-term market sustainability, as more patients seek preventive measures rather than relying solely on acute treatments.

Key Market Drivers

Advancements in Research and Development (R&D)

Advancements in Research and Development (R&D) have been pivotal in boosting the Global Hereditary Angioedema Therapeutics Market. Hereditary Angioedema is a rare genetic disorder characterized by debilitating and unpredictable swelling episodes that can be life-threatening. In recent years, the relentless pursuit of scientific knowledge and innovative therapies has transformed the landscape of HAE treatment.

One of the most significant drivers of market growth has been the breakthrough discoveries in understanding the underlying mechanisms of HAE. Researchers have delved deep into the genetic and biochemical aspects of the disease, leading to a more precise understanding of how it develops and progresses. This increased knowledge has paved the way for the development of targeted therapies that are specifically designed to address the root causes of HAE.

Monoclonal antibodies, in particular, have emerged as a revolutionary approach in HAE therapeutics. These monoclonal antibodies, such as lanadelumab and ecallantide, have been engineered to specifically inhibit the activity of proteins like plasma kallikrein, which play a critical role in HAE attacks. This precision in drug design has proven highly effective in preventing and managing HAE episodes, providing patients with newfound hope and relief from the burden of their condition.

Key Market Challenges

High Treatment Costs

The High treatment costs have emerged as a significant obstacle hindering the growth and accessibility of the Global Hereditary Angioedema Therapeutics Market. HAE is a rare genetic disorder characterized by recurrent and potentially life-threatening swelling episodes. While advancements in therapeutics have improved the quality of life for HAE patients, the exorbitant cost of these treatments poses a considerable challenge. The prohibitively high cost of treatment makes these life-saving therapies inaccessible to a substantial portion of HAE patients, especially those without comprehensive health insurance coverage. This leads to disparities in access to care, with only a fraction of those in need benefiting from the latest advancements in HAE therapeutics.

For individuals who manage to access HAE therapies, the financial strain can be overwhelming. Copayments, deductibles, and out-of-pocket expenses can quickly accumulate, potentially forcing patients to make difficult choices between their healthcare needs and other essential expenses.

Access to HAE treatments is even more challenging in regions with limited healthcare resources and lower income levels. This exacerbates global healthcare disparities, where patients in wealthier nations have greater access to cutting-edge treatments, while those in less affluent regions struggle to secure even basic care.

Key Market Trends

Personalized Medicine Approaches

Hereditary angioedema (HAE) is a rare genetic disorder characterized by recurrent episodes of severe swelling in various body parts, including the extremities, face, gastrointestinal tract, and airway. This condition is caused by mutations in the SERPING1 gene, leading to deficient or dysfunctional C1 inhibitor (C1-INH) proteins, which play a crucial role in regulating inflammatory pathways.

Personalized medicine has significantly advanced the management of HAE by tailoring treatments to individual genetic profiles and disease manifestations. The process begins with precise genetic testing to identify specific mutations in the SERPING1 gene, which helps determine the subtype of HAE a patient has. This accurate diagnosis is essential, as it guides the selection of targeted therapies that address the underlying pathophysiological mechanisms.

For instance, patients with Type I HAE, characterized by low levels of functional C1-INH, may benefit from C1-INH replacement therapies such as Berinert or Cinryze. These treatments work by supplementing the deficient protein, thereby preventing or reducing the frequency of swelling episodes. Conversely, patients with normal C1-INH levels but dysfunctional protein (Type II HAE) might respond better to therapies that inhibit the kallikrein-kinin pathway, such as lanadelumab (Takhzyro), a monoclonal antibody that targets plasma kallikrein to prevent bradykinin formation, a key mediator of swelling in HAE.

Key Market Players

Report Scope:

In this report, the Global Hereditary Angioedema Therapeutics Market has been segmented into the following categories, in addition to the industry trends which have also been detailed below:

Hereditary Angioedema Therapeutics Market, By Drug Class:

Hereditary Angioedema Therapeutics Market, By Distribution Channel:

Hereditary Angioedema Therapeutics Market, By Application:

Hereditary Angioedema Therapeutics Market, By Region:

Competitive Landscape

Company Profiles: Detailed analysis of the major companies present in the Global Hereditary Angioedema Therapeutics Market.

Available Customizations:

Global Hereditary Angioedema Therapeutics Market report with the given market data, TechSci Research offers customizations according to a company's specific needs. The following customization options are available for the report:

Company Information

Table of Contents

1. Product Overview

2. Research Methodology

3. Executive Summary

4. Global Hereditary Angioedema Therapeutics Market Outlook

5. Asia Pacific Hereditary Angioedema Therapeutics Market Outlook

6. Europe Hereditary Angioedema Therapeutics Market Outlook

7. North America Hereditary Angioedema Therapeutics Market Outlook

8. South America Hereditary Angioedema Therapeutics Market Outlook

9. Middle East and Africa Hereditary Angioedema Therapeutics Market Outlook

10. Market Dynamics

11. Market Trends & Developments

12. Global Hereditary Angioedema Therapeutics Market: SWOT Analysis

13. Porter's Five Forces Analysis

14. Competitive Landscape

15. Strategic Recommendations

16. About Us & Disclaimer

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