시장보고서
상품코드
2018403

유전성 혈관부종 치료제 시장 규모, 점유율, 동향 분석 보고서 : 치료법별, 용도별, 지역별, 부문별 예측(2026-2033년)

Hereditary Angioedema Therapeutics Market Size, Share & Trends Analysis Report By Treatment (C1-Inhibitor Concentrates, Bradykinin B2 Receptor Antagonist), By End Use, By Region, And Segment Forecasts, 2026 - 2033

발행일: | 리서치사: 구분자 Grand View Research | 페이지 정보: 영문 150 Pages | 배송안내 : 2-10일 (영업일 기준)

    
    
    




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유전성 혈관성 부종 치료제 시장 개요

세계의 유전성 혈관부종 치료제 시장 규모는 2025년에 36억 달러로 추정되며, 2033년까지 81억 8,000만 달러에 달할 것으로 예측되며, 2026년부터 2033년까지 CAGR 10.43%로 성장할 것으로 전망됩니다.

전 세계 유전성 혈관부종 치료제 시장은 진단율 향상과 희귀 유전성 질환에 대한 임상적 인식이 높아짐에 따라 확대되고 있습니다.

전문적인 검사에 대한 접근성이 개선되어 환자의 조기 발견이 가능해졌고, 적시에 치료를 시작할 수 있게 되었습니다. 질병의 근본적인 기전에 작용하는 표적 치료제가 가능해짐에 따라 치료 성과와 환자들의 신뢰가 높아지고 있습니다. 제약 분야의 혁신으로 피하투여, 경구제제 등 복약 순응도를 높일 수 있는 편리한 투약 방법이 도입되었습니다. 선진국과 신흥 지역에서 유병률 보고가 증가함에 따라 효과적인 치료법에 대한 수요가 지속적으로 증가하고 있습니다.

바이오의약품과 새로운 약물의 발전은 시장의 또 다른 주요 성장 요인으로 작용하고 있습니다. 장기지속형 예방요법은 발작 빈도를 감소시키고 환자의 삶의 질을 향상시킴으로써 의사들의 채택이 증가하고 있습니다. 현재 개발 중인 경구용 칼리크레인 억제제 및 유전자 표적 치료제는 미래의 치료 옵션을 넓히고 있습니다. 활발한 임상시험 활동과 규제 당국의 승인으로 혁신적인 치료제의 시장 출시 일정이 가속화되고 있습니다. 예를 들어, 2025년 12월 HCPLive는 미국 식품의약국(FDA)이 2025년 3개월 동안 갈라다시맙 GXII, 6월 안뎀브리(Andembry), 7월 세베트랄스타트(Ekterly), 8월 도니달로센(Dawnzera)을 승인했습니다. 이 질환은 전 세계적으로 약 5만 명 중 1명, 미국에서는 약 6,000명이 앓고 있습니다. 승인 이전에는 9가지 치료법이 있었지만, 경구 및 주사제 선택의 폭이 넓어짐에 따라 2026년까지 12가지로 늘어날 것으로 예상됩니다. 생명공학기업과 대형 제약사와의 전략적 제휴를 통해 연구 역량과 세계 유통망을 더욱 강화했습니다.

의료 인프라의 개선과 전문 의료 네트워크의 확대도 시장 성장에 더욱 기여하고 있습니다. 면역학자와 희귀질환 전문의의 참여가 증가함에 따라 질병 관리 기준과 치료의 활용도가 높아졌습니다. 환자 지원 활동과 교육 프로그램은 치료의 수용과 장기적인 치료 순응도를 높이고 있습니다. 일부 지역에서의 유리한 보험 환급 제도는 고가의 생물학적 제제에 대한 환자의 접근성을 향상시켰습니다. 예를 들어, 2025년 12월 Rare Disease Advisor는 미국 식품의약국(FDA)이 ORLADEYO로 판매되는 벨로트랄스타트를 2세에서 11세 사이의 소아에서 유전성 혈관성 부종에 대한 최초의 경구용 혈장 칼리크레인 억제제 예방요법으로 승인했다고 보도했습니다. 이로써 기존 12세 이상 환자에 대한 승인 범위가 확대되었습니다. 이번 소아 승인은 2-11세 환자 29명(여성 48.3%)을 대상으로 한 APeX P 임상을 기반으로 했습니다. 평균 연령은 8세, 발병 평균 연령은 2세였으며, 월별 발작 빈도의 지속적인 감소와 최고 혈중 농도 도달 시간 중앙값 3.9시간(범위 0.9-6.0시간)을 보였습니다. 희귀질환 연구에 대한 투자 확대는 혁신과 경쟁력 있는 시장 확대를 지속적으로 뒷받침하고 있습니다.

자주 묻는 질문

  • 유전성 혈관성 부종 치료제 시장 규모는 어떻게 예측되나요?
  • 유전성 혈관성 부종 치료제 시장의 성장 요인은 무엇인가요?
  • 현재 유전성 혈관성 부종 치료제의 승인된 치료법은 몇 가지인가요?
  • 유전성 혈관성 부종 치료제 시장에서 바이오의약품의 역할은 무엇인가요?
  • 유전성 혈관성 부종 치료제 시장의 의료 인프라 개선은 어떤 영향을 미치고 있나요?

목차

제1장 조사 방법과 범위

제2장 주요 요약

제3장 유전성 혈관부종 치료제 시장 : 변수, 동향, 범위

제4장 유전성 혈관부종 치료제 시장 : 치료별 비즈니스 분석

제5장 유전성 혈관부종 치료제 시장 : 최종사용별 비즈니스 분석

제6장 유전성 혈관부종 치료제 시장 : 투여 경로별 비즈니스 분석

제7장 유전성 혈관부종 치료제 시장 : 지역별 추정·동향 분석

제8장 경쟁 구도

KSM 26.05.13

Hereditary Angioedema Therapeutics Market Summary

The global hereditary angioedema therapeutics market size was estimated at USD 3.60 billion in 2025 and is projected to reach USD 8.18 billion by 2033, growing at a CAGR of 10.43% from 2026 to 2033. The global hereditary angioedema therapeutics market is expanding due to increasing diagnosis rates and greater clinical awareness of rare genetic disorders.

Improved access to specialized testing has enabled earlier identification of patients, which supports timely treatment initiation. The availability of targeted therapies that address underlying disease pathways has strengthened treatment outcomes and patient confidence. Pharmaceutical innovation has introduced convenient administration options, including subcutaneous and oral formulations, which improve adherence. Rising prevalence reporting across developed and emerging regions continues to create sustained demand for effective therapies.

Advancements in biologics and novel drug classes represent another major growth driver for the market. Long-acting prophylactic therapies have reduced attack frequency and improved quality of life for patients, which has increased adoption among physicians. Oral kallikrein inhibitors and gene-targeted approaches under development are expanding the future treatment landscape. Strong clinical trial activity and regulatory approvals have accelerated commercialization timelines for innovative therapies. For instance, December 2025, HCPLive reported that the U.S. Food and Drug Administration had approved three new hereditary angioedema treatments in 2025 over three months, including garadacimab gxii, Andembry, in June, sebetralstat, Ekterly, in July, and donidalorsen, Dawnzera, in August, in a disease affecting about 1 in 50,000 people globally and nearly 6,000 in the United States. Prior to these approvals, 9 therapies were available, increasing to 12 by 2026, reflecting the expansion of oral and injectable options. Strategic collaborations between biotechnology firms and larger pharmaceutical companies have further enhanced research capabilities and global distribution reach.

Healthcare infrastructure improvements and the expansion of specialty care networks are further contributing to market growth. Increased involvement of immunologists and rare disease specialists has strengthened disease management standards and treatment utilization. Patient advocacy initiatives and education programs have encouraged treatment uptake and long-term therapy compliance. Favorable reimbursement coverage in several regions has improved patient access to high-cost biologic treatments. For instance, in December 2025, Rare Disease Advisor reported that the U.S. Food and Drug Administration had approved berotralstat, marketed as ORLADEYO, as the first oral plasma kallikrein inhibitor prophylactic therapy for hereditary angioedema in children aged 2 to 11 years, extending prior approval for patients 12 years and older. The pediatric approval was based on the APeX P trial involving 29 patients aged 2 to 11 years, 48.3 percent female, with a mean age of 8 years and a mean onset at 2 years, demonstrating sustained reductions in monthly attack rates and a peak median concentration of 3.9 hours, range 0.9 to 6.0 hours. Growing investment in rare disease research continues to support innovation and competitive market expansion.

Global Hereditary Angioedema Therapeutics Market Report Segmentation

This report forecasts revenue growth at global, regional, and country levels and provides an analysis of the latest industry trends in each of the sub-segments from 2021 to 2033. For this study, Grand View Research has segmented the global hereditary angioedema therapeutics market based on treatment, end use, route of administration, and region:

  • Treatment Outlook (Revenue, USD Million, 2021 - 2033)
  • C1-Inhibitor Concentrates
  • Bradykinin B2 Receptor Antagonist
  • Kallikrein Inhibitor
  • Others
  • End use Outlook (Revenue, USD Million, 2021 - 2033)
  • Prophylaxis
  • On-demand
  • Route of Administration Outlook (Revenue, USD Million, 2021 - 2033)
  • Intravenous
  • Subcutaneous
  • Oral
  • Regional Outlook (Revenue, USD Million, 2021 - 2033)
  • North America
    • U.S.
    • Canada
    • Mexico
  • Europe
    • UK
    • Germany
    • France
    • Italy
    • Spain
    • Denmark
    • Sweden
    • Norway
  • Asia Pacific
    • Japan
    • China
    • India
    • Australia
    • South Korea
    • Thailand
  • Latin America
    • Brazil
    • Argentina
  • Middle East & Africa
    • South Africa
    • Saudi Arabia
    • UAE
    • Kuwait

Table of Contents

Chapter 1. Methodology and Scope

  • 1.1. Market Segmentation & Scope
  • 1.2. Segment Definitions
    • 1.2.1. Treatment
    • 1.2.2. End Use
    • 1.2.3. Route of Administration
  • 1.3. Estimates and Forecast Timeline
  • 1.4. Research Methodology
  • 1.5. Information Procurement
    • 1.5.1. Purchased Database
    • 1.5.2. GVR's Internal Database
    • 1.5.3. Secondary Sources
    • 1.5.4. Primary Research
  • 1.6. Information Analysis
    • 1.6.1. Data Analysis Models
  • 1.7. Market Formulation & Data Visualization
  • 1.8. Model Details
    • 1.8.1. Commodity Flow Analysis
  • 1.9. List of Secondary Sources
  • 1.10. Objectives

Chapter 2. Executive Summary

  • 2.1. Market Snapshot
  • 2.2. Segment Snapshot
  • 2.3. Competitive Landscape Snapshot

Chapter 3. Hereditary Angioedema Therapeutics Market Variables, Trends, & Scope

  • 3.1. Market Lineage Outlook
  • 3.2. Market Dynamics
    • 3.2.1. Market Driver Analysis
    • 3.2.2. Market Restraint Analysis
  • 3.3. Business Environment Analysis
    • 3.3.1. Industry Analysis - Porter's Five Forces Analysis
      • 3.3.1.1. Supplier Power
      • 3.3.1.2. Buyer Power
      • 3.3.1.3. Substitution Threat
      • 3.3.1.4. Threat of New Entrants
      • 3.3.1.5. Competitive Rivalry
    • 3.3.2. PESTLE Analysis
    • 3.3.3. Pipeline Analysis
    • 3.3.4. Patent Expiry Analysis
    • 3.3.5. Pricing Analysis

Chapter 4. Hereditary Angioedema Therapeutics Market: Treatment Business Analysis

  • 4.1. Treatment Market Share, 2025 & 2033
  • 4.2. Treatment Segment Dashboard
  • 4.3. Market Size & Forecasts and Trend Analysis, by Treatment, 2021 to 2033 (USD Million)
  • 4.4. C1-Inhibitor Concentrates
    • 4.4.1. C1-Inhibitor Concentrates Market, 2021 - 2033 (USD Million)
  • 4.5. Bradykinin B2 Receptor Antagonist
    • 4.5.1. Bradykinin B2 Receptor Antagonist Market, 2021 - 2033 (USD Million)
  • 4.6. Kallikrein Inhibitor
    • 4.6.1. Kallikrein Inhibitor Market, 2021 - 2033 (USD Million)
  • 4.7. Others
    • 4.7.1. Others Market, 2021 - 2033 (USD Million)

Chapter 5. Hereditary Angioedema Therapeutics Market: End Use Business Analysis

  • 5.1. End Use Market Share, 2025 & 2033
  • 5.2. End Use Segment Dashboard
  • 5.3. Market Size & Forecasts and Trend Analysis, by End Use, 2021 to 2033 (USD Million)
  • 5.4. Prophylaxis
    • 5.4.1. Prophylaxis Market, 2021 - 2033 (USD Million)
  • 5.5. On-demand
    • 5.5.1. On-demand Market, 2021 - 2033 (USD Million)

Chapter 6. Hereditary Angioedema Therapeutics Market: Route of Administration Business Analysis

  • 6.1. Route of Administration Market Share, 2025 & 2033
  • 6.2. Route of Administration Segment Dashboard
  • 6.3. Market Size & Forecasts and Trend Analysis, by Route of administration, 2021 to 2033 (USD Million)
  • 6.4. Intravenous
    • 6.4.1. Intravenous Market, 2021 - 2033 (USD Million)
  • 6.5. Subcutaneous
    • 6.5.1. Subcutaneous Market, 2021 - 2033 (USD Million)
  • 6.6. Oral
    • 6.6.1. Oral Market, 2021 - 2033 (USD Million)

Chapter 7. Hereditary Angioedema Therapeutics Market: Regional Estimates & Trend Analysis

  • 7.1. Regional Market Share Analysis, 2025 & 2033
  • 7.2. Regional Market Dashboard
  • 7.3. Market Size & Forecasts Trend Analysis, 2021 to 2033:
  • 7.4. North America
    • 7.4.1. North America Hereditary Angioedema Therapeutics Market Estimates and Forecasts, By Country, 2021 - 2033 (USD Million)
    • 7.4.2. U.S.
      • 7.4.2.1. Key Country Dynamics
      • 7.4.2.2. End Use Disease Prevalence
      • 7.4.2.3. Regulatory Framework
      • 7.4.2.4. Reimbursement Framework
      • 7.4.2.5. U.S. Hereditary Angioedema Therapeutics Market Estimates and Forecasts, 2021 - 2033 (USD Million)
    • 7.4.3. Canada
      • 7.4.3.1. Key Country Dynamics
      • 7.4.3.2. End Use Disease Prevalence
      • 7.4.3.3. Regulatory Framework
      • 7.4.3.4. Reimbursement Framework
      • 7.4.3.5. U.S. Hereditary Angioedema Therapeutics Market Estimates and Forecasts, 2021 - 2033 (USD Million)
    • 7.4.4. Mexico
      • 7.4.4.1. Key Country Dynamics
      • 7.4.4.2. End Use Disease Prevalence
      • 7.4.4.3. Regulatory Framework
      • 7.4.4.4. Reimbursement Framework
      • 7.4.4.5. Mexico Hereditary Angioedema Therapeutics Market Estimates and Forecasts, 2021 - 2033 (USD Million)
  • 7.5. Europe
    • 7.5.1. Europe Hereditary Angioedema Therapeutics Market Estimates and Forecasts, 2021 - 2033 (USD Million)
    • 7.5.2. UK
      • 7.5.2.1. Key Country Dynamics
      • 7.5.2.2. End Use Disease Prevalence
      • 7.5.2.3. Regulatory Framework
      • 7.5.2.4. Reimbursement Framework
      • 7.5.2.5. Uk Hereditary Angioedema Therapeutics Market Estimates and Forecasts, 2021 - 2033 (USD Million)
    • 7.5.3. Germany
      • 7.5.3.1. Key Country Dynamics
      • 7.5.3.2. End Use Disease Prevalence
      • 7.5.3.3. Regulatory Framework
      • 7.5.3.4. Reimbursement Framework
      • 7.5.3.5. Germany Hereditary Angioedema Therapeutics Market Estimates and Forecasts, 2021 - 2033 (USD Million)
    • 7.5.4. France
      • 7.5.4.1. Key Country Dynamics
      • 7.5.4.2. End Use Disease Prevalence
      • 7.5.4.3. Regulatory Framework
      • 7.5.4.4. Reimbursement Framework
      • 7.5.4.5. France Hereditary Angioedema Therapeutics Market Estimates and Forecasts, 2021 - 2033 (USD Million)
    • 7.5.5. Italy
      • 7.5.5.1. Key Country Dynamics
      • 7.5.5.2. End Use Disease Prevalence
      • 7.5.5.3. Regulatory Framework
      • 7.5.5.4. Reimbursement Framework
      • 7.5.5.5. Italy Hereditary Angioedema Therapeutics Market Estimates and Forecasts, 2021 - 2033 (USD Million)
    • 7.5.6. Spain
      • 7.5.6.1. Key Country Dynamics
      • 7.5.6.2. End Use Disease Prevalence
      • 7.5.6.3. Regulatory Framework
      • 7.5.6.4. Reimbursement Framework
      • 7.5.6.5. Spain Hereditary Angioedema Therapeutics Market Estimates and Forecasts, 2021 - 2033 (USD Million)
    • 7.5.7. Denmark
      • 7.5.7.1. Key Country Dynamics
      • 7.5.7.2. End Use Disease Prevalence
      • 7.5.7.3. Regulatory Framework
      • 7.5.7.4. Reimbursement Framework
      • 7.5.7.5. Denmark Hereditary Angioedema Therapeutics Market Estimates and Forecasts, 2021 - 2033 (USD Million)
    • 7.5.8. Sweden
      • 7.5.8.1. Key Country Dynamics
      • 7.5.8.2. End Use Disease Prevalence
      • 7.5.8.3. Regulatory Framework
      • 7.5.8.4. Reimbursement Framework
      • 7.5.8.5. Sweden Hereditary Angioedema Therapeutics Market Estimates and Forecasts, 2021 - 2033 (USD Million)
    • 7.5.9. Norway
      • 7.5.9.1. Key Country Dynamics
      • 7.5.9.2. End Use Disease Prevalence
      • 7.5.9.3. Regulatory Framework
      • 7.5.9.4. Reimbursement Framework
      • 7.5.9.5. Norway Hereditary Angioedema Therapeutics Market Estimates and Forecasts, 2021 - 2033 (USD Million)
  • 7.6. Asia Pacific
    • 7.6.1. Asia Pacific Hereditary Angioedema Therapeutics Market Estimates and Forecasts, 2021 - 2033 (USD Million)
    • 7.6.2. Japan
      • 7.6.2.1. Key Country Dynamics
      • 7.6.2.2. End Use Disease Prevalence
      • 7.6.2.3. Regulatory Framework
      • 7.6.2.4. Reimbursement Framework
      • 7.6.2.5. Japan Hereditary Angioedema Therapeutics Market Estimates and Forecasts, 2021 - 2033 (USD Million)
    • 7.6.3. China
      • 7.6.3.1. Key Country Dynamics
      • 7.6.3.2. End Use Disease Prevalence
      • 7.6.3.3. Regulatory Framework
      • 7.6.3.4. Reimbursement Framework
      • 7.6.3.5. China Hereditary Angioedema Therapeutics Market Estimates and Forecasts, 2021 - 2033 (USD Million)
    • 7.6.4. India
      • 7.6.4.1. Key Country Dynamics
      • 7.6.4.2. End Use Disease Prevalence
      • 7.6.4.3. Regulatory Framework
      • 7.6.4.4. Reimbursement Framework
      • 7.6.4.5. India Hereditary Angioedema Therapeutics Market Estimates and Forecasts, 2021 - 2033 (USD Million)
    • 7.6.5. Australia
      • 7.6.5.1. Key Country Dynamics
      • 7.6.5.2. End Use Disease Prevalence
      • 7.6.5.3. Regulatory Framework
      • 7.6.5.4. Reimbursement Framework
      • 7.6.5.5. Australia Hereditary Angioedema Therapeutics Market Estimates and Forecasts, 2021 - 2033 (USD Million)
    • 7.6.6. South Korea
      • 7.6.6.1. Key Country Dynamics
      • 7.6.6.2. End Use Disease Prevalence
      • 7.6.6.3. Regulatory Framework
      • 7.6.6.4. Reimbursement Framework
      • 7.6.6.5. South Korea Hereditary Angioedema Therapeutics Market Estimates and Forecasts, 2021 - 2033 (USD Million)
    • 7.6.7. Thailand
      • 7.6.7.1. Key Country Dynamics
      • 7.6.7.2. End Use Disease Prevalence
      • 7.6.7.3. Regulatory Framework
      • 7.6.7.4. Reimbursement Framework
      • 7.6.7.5. Thailand Hereditary Angioedema Therapeutics Market Estimates and Forecasts, 2021 - 2033 (USD Million)
  • 7.7. Latin America
    • 7.7.1. Latin America Hereditary Angioedema Therapeutics Market Estimates and Forecasts, 2021 - 2033 (USD Million)
    • 7.7.2. Brazil
      • 7.7.2.1. Key Country Dynamics
      • 7.7.2.2. End Use Disease Prevalence
      • 7.7.2.3. Regulatory Framework
      • 7.7.2.4. Reimbursement Framework
      • 7.7.2.5. Japan Hereditary Angioedema Therapeutics Market Estimates and Forecasts, 2021 - 2033 (USD Million)
    • 7.7.3. Argentina
      • 7.7.3.1. Key Country Dynamics
      • 7.7.3.2. End Use Disease Prevalence
      • 7.7.3.3. Regulatory Framework
      • 7.7.3.4. Reimbursement Framework
      • 7.7.3.5. China Hereditary Angioedema Therapeutics Market Estimates and Forecasts, 2021 - 2033 (USD Million)
  • 7.8. Middle East and Africa
    • 7.8.1. Middle East and Africa Hereditary Angioedema Therapeutics Market Estimates and Forecasts, 2021 - 2033 (USD Million)
    • 7.8.2. South Africa
      • 7.8.2.1. Key Country Dynamics
      • 7.8.2.2. End Use Disease Prevalence
      • 7.8.2.3. Regulatory Framework
      • 7.8.2.4. Reimbursement Framework
      • 7.8.2.5. South Africa Hereditary Angioedema Therapeutics Market Estimates and Forecasts, 2021 - 2033 (USD Million)
    • 7.8.3. Saudi Arabia
      • 7.8.3.1. Key Country Dynamics
      • 7.8.3.2. End Use Disease Prevalence
      • 7.8.3.3. Regulatory Framework
      • 7.8.3.4. Reimbursement Framework
      • 7.8.3.5. Saudi Arabia Hereditary Angioedema Therapeutics Market Estimates and Forecasts, 2021 - 2033 (USD Million)
    • 7.8.4. UAE
      • 7.8.4.1. Key Country Dynamics
      • 7.8.4.2. End Use Disease Prevalence
      • 7.8.4.3. Regulatory Framework
      • 7.8.4.4. Reimbursement Framework
      • 7.8.4.5. UAE Hereditary Angioedema Therapeutics Market Estimates and Forecasts, 2021 - 2033 (USD Million)
    • 7.8.5. Kuwait
      • 7.8.5.1. Key Country Dynamics
      • 7.8.5.2. End Use Disease Prevalence
      • 7.8.5.3. Regulatory Framework
      • 7.8.5.4. Reimbursement Framework
      • 7.8.5.5. Kuwait Hereditary Angioedema Therapeutics Market Estimates and Forecasts, 2021 - 2033 (USD Million)

Chapter 8. Competitive Landscape

  • 8.1. Participant Overview
  • 8.2. Company Market Position Analysis
  • 8.3. Company Categorization
  • 8.4. Strategy Mapping
  • 8.5. Company Profiles/Listing
    • 8.5.1. BioCryst Pharmaceuticals, Inc.
      • 8.5.1.1. Overview
      • 8.5.1.2. Financial Performance
      • 8.5.1.3. Treatment Benchmarking
      • 8.5.1.4. Strategic Initiatives
    • 8.5.2. Ionis Pharmaceuticals
      • 8.5.2.1. Overview
      • 8.5.2.2. Financial Performance
      • 8.5.2.3. Treatment Benchmarking
      • 8.5.2.4. Strategic Initiatives
    • 8.5.3. CSL
      • 8.5.3.1. Overview
      • 8.5.3.2. Financial Performance
      • 8.5.3.3. Treatment Benchmarking
      • 8.5.3.4. Strategic Initiatives
    • 8.5.4. Attune Pharmaceuticals
      • 8.5.4.1. Overview
      • 8.5.4.2. Financial Performance
      • 8.5.4.3. Treatment Benchmarking
      • 8.5.4.4. Strategic Initiatives
    • 8.5.5. Adverum Biotechnologies, Inc.
      • 8.5.5.1. Overview
      • 8.5.5.2. Financial Performance
      • 8.5.5.3. Treatment Benchmarking
      • 8.5.5.4. Strategic Initiatives
    • 8.5.6. KalVista Pharmaceuticals, Inc.
      • 8.5.6.1. Overview
      • 8.5.6.2. Financial Performance
      • 8.5.6.3. Treatment Benchmarking
      • 8.5.6.4. Strategic Initiatives
    • 8.5.7. Takeda Pharmaceutical Company Limited
      • 8.5.7.1. Overview
      • 8.5.7.2. Financial Performance
      • 8.5.7.3. Treatment Benchmarking
      • 8.5.7.4. Strategic Initiatives
    • 8.5.8. Pharming
      • 8.5.8.1. Overview
      • 8.5.8.2. Financial Performance
      • 8.5.8.3. Treatment Benchmarking
      • 8.5.8.4. Strategic Initiatives
    • 8.5.9. Sanofi
      • 8.5.9.1. Overview
      • 8.5.9.2. Financial Performance
      • 8.5.9.3. Treatment Benchmarking
      • 8.5.9.4. Strategic Initiatives
    • 8.5.10. Pharvaris B.V.
      • 8.5.10.1. Overview
      • 8.5.10.2. Financial Performance
      • 8.5.10.3. Treatment Benchmarking
      • 8.5.10.4. Strategic Initiatives
    • 8.5.11. Arrowhead Pharmaceuticals, Inc.
      • 8.5.11.1. Overview
      • 8.5.11.2. Financial Performance
      • 8.5.11.3. Treatment Benchmarking
      • 8.5.11.4. Strategic Initiatives
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