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市場調査レポート
商品コード
1653949
特発性肺線維症治療市場規模、シェア、成長分析:薬剤クラス別、投与経路別、作用機序別、流通チャネル別、最終用途別、地域別 - 産業予測 2025~2032年Idiopathic Pulmonary Fibrosis Treatment Market Size, Share, and Growth Analysis, By Drug Class, By Route of Administration, By Mode of Action, By Distribution Channel, By End-use, By Region - Industry Forecast 2025-2032 |
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特発性肺線維症治療市場規模、シェア、成長分析:薬剤クラス別、投与経路別、作用機序別、流通チャネル別、最終用途別、地域別 - 産業予測 2025~2032年 |
出版日: 2025年02月10日
発行: SkyQuest
ページ情報: 英文 157 Pages
納期: 3~5営業日
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特発性肺線維症治療市場規模は2023年に46億米ドルと評価され、2024年の49億2,000万米ドルから2032年には83億9,000万米ドルに成長し、予測期間(2025-2032年)のCAGRは6.9%で成長する見通しです。
世界の特発性肺線維症(IPF)治療市場は、主に人口の増加と呼吸器疾患に対する意識の高まりによって、大幅な成長を遂げています。IPFは、呼吸を障害する肺の瘢痕化を特徴とし、肺線維症の主流です。現在の治療法には、ニンテダニブやピルフェニドンといったFDA承認の薬理療法がある一方、進行した患者には肺移植が有効な解決策となっています。近年、研究開発活動が急増し、有望な治療法の革新や新薬候補が生み出されています。さらに、製薬企業と研究機関の戦略的提携が効果的なIPF治療法の開発を後押しし、市場ダイナミクスをさらに活性化させ、患者の治療成果を向上させています。
Idiopathic Pulmonary Fibrosis Treatment Market size was valued at USD 4.6 billion in 2023 and is poised to grow from USD 4.92 billion in 2024 to USD 8.39 billion by 2032, growing at a CAGR of 6.9% during the forecast period (2025-2032).
The global idiopathic pulmonary fibrosis (IPF) treatment market has seen substantial growth, primarily driven by an increasing population and heightened awareness of respiratory diseases. IPF, characterized by lung scarring that impairs breathing, is the predominant form of pulmonary fibrosis. Current treatment options include FDA-approved pharmacological therapies like Nintedanib and Pirfenidone, while lung transplantation remains a viable solution for patients in advanced stages of the disease. Recent years have witnessed a surge in R&D activities, resulting in promising therapeutic innovations and new drug candidates. Moreover, strategic collaborations between pharmaceutical companies and research institutions are propelling the development of effective IPF treatments, further invigorating market dynamics and enhancing patient care outcomes.
Top-down and bottom-up approaches were used to estimate and validate the size of the Idiopathic Pulmonary Fibrosis Treatment market and to estimate the size of various other dependent submarkets. The research methodology used to estimate the market size includes the following details: The key players in the market were identified through secondary research, and their market shares in the respective regions were determined through primary and secondary research. This entire procedure includes the study of the annual and financial reports of the top market players and extensive interviews for key insights from industry leaders such as CEOs, VPs, directors, and marketing executives. All percentage shares split, and breakdowns were determined using secondary sources and verified through Primary sources. All possible parameters that affect the markets covered in this research study have been accounted for, viewed in extensive detail, verified through primary research, and analyzed to get the final quantitative and qualitative data.
Idiopathic Pulmonary Fibrosis Treatment Market Segments Analysis
Global Idiopathic Pulmonary Fibrosis Treatment Market is segmented by Drug Class, Route of Administration, Mode of Action, Distribution Channel, End-use and region. Based on Drug Class, the market is segmented into Pirfenidone, Nintedanib and Others. Based on Route of Administration, the market is segmented into Oral and Injectable. Based on Mode of Action, the market is segmented into Antifibrotic Agents, Tyrosine Kinase Inhibitors and Others. Based on Distribution Channel, the market is segmented into Hospital Pharmacies, Retail Pharmacies and Online Pharmacies. Based on End-use, the market is segmented into Hospitals, Clinics and Homecare Settings. Based on region, the market is segmented into North America, Europe, Asia Pacific, Latin America and Middle East & Africa.
Driver of the Idiopathic Pulmonary Fibrosis Treatment Market
A significant factor propelling the Global Idiopathic Pulmonary Fibrosis (IPF) Treatment Market is the growing incidence of IPF, especially among the elderly demographic. As the disease becomes more common worldwide, there is an escalating demand for effective treatment modalities. This increase in diagnosed cases highlights the urgent need for pharmaceutical solutions and therapies that can not only decelerate the progression of the disease but also enhance the overall quality of life for patients. Consequently, the continual rise in the prevalence of IPF serves as a vital driver for the expansion and innovation within this treatment market.
Restraints in the Idiopathic Pulmonary Fibrosis Treatment Market
A significant challenge facing the idiopathic pulmonary fibrosis (IPF) treatment market is the prohibitive cost associated with therapies. The expenses tied to medications and diagnostic procedures can be substantial, potentially restricting access to essential treatments, particularly in areas where healthcare resources are scarce or insurance coverage is insufficient. This financial barrier can hinder the availability and affordability of effective therapeutic options, ultimately affecting patient outcomes and limiting the overall growth potential of the IPF treatment market in various regions, particularly those with less developed healthcare infrastructure. Addressing these cost-related issues is crucial for improving patient access to necessary care.
Market Trends of the Idiopathic Pulmonary Fibrosis Treatment Market
The idiopathic pulmonary fibrosis (IPF) treatment market is witnessing a significant shift towards personalized medicine and precision therapeutics, reflecting a broader trend in healthcare. As research progresses, the emphasis has moved from understanding the disease's pathogenesis to developing tailored treatment strategies aimed at individual patient profiles. Notable advancements in pharmacotherapy, particularly with the introduction of Nintedanib and Pirfenidone, have demonstrated efficacy in slowing the decline in forced vital capacity (FVC) and improving patient quality of life. This growing focus on individualized treatment plans is poised to drive market growth, as stakeholders aim to enhance therapeutic outcomes and optimize patient care in IPF management.