特発性肺線維症市場- 世界の産業規模、シェア、動向、機会、予測、薬剤の種類別、投与経路別、流通チャネル別、地域別、競合別、2020～2030年

肺特発性肺線維症（IPF）市場は2024年に36億4,000万米ドルと評価され、予測期間中のCAGRは6.72%で2030年には53億9,000万米ドルに達すると予測されています。

肺疾患特発性肺線維症（IPF）は危険です。息を吸うと、酸素は肺の小さな気嚢を通って血流に入る。その後、酸素は体内の臓器に運ばれます。2022年7月に発表されたPrescriber社の疫学データによると、欧州における特発性肺線維症の年間発症率は10万人当たり0.22～7.4人で、英国だけで約32,500人の症例が報告されています。

IPFにより肺が瘢痕組織でうっ血します。時間の経過とともに、瘢痕組織は悪化します。切り傷を負った後の皮膚の傷のように、IPFの瘢痕組織は緻密です。瘢痕組織は肺から血液への酸素の移行を阻害し、身体が正常に機能しなくなる可能性があります。特発性肺線維症は、症状が現れないまま非常に長い間存在することがあります。公害や特定の薬、病気などにさらされると、肺線維症になることがあります。しかし、IPFの原因が何であるかについては、医師もよくわかっていないです。

IPFの診断には、病歴、身体診察、肺機能検査、高分解能コンピュータ断層撮影（HRCT）スキャン、そして場合によっては肺生検を組み合わせる必要があります。IPFは他の肺疾患と症状が重複することがあるため、診断が難しいことが多いです。高解像度コンピュータ断層撮影（HRCT）やバイオマーカーの同定などの診断技術の向上により、IPFの早期かつ正確な発見が可能となりました。これにより、治療を希望する患者数が増加しています。IPFに対する新薬や治療法の継続的な研究開発により、新たな治療法が導入され、患者にとって利用可能な選択肢が広がっています。革新的な治療法の承認は市場の原動力となっています。IPFの症状や早期診断の重要性に関する啓蒙キャンペーンや教育的イニシアチブの増加により、医療を求める患者が増加しています。ヘルスケアの専門家もIPFを認識する能力が向上しています。サポートグループや患者支援活動、IPF患者の生活の質の向上など、患者中心のケアに重点を置くことが市場の促進要因となっています。患者支援団体は、認知度の向上と患者ケアの改善に重要な役割を果たしています。

主な市場促進要因

診断の進歩

主な市場課題

治療費の高騰

主な市場動向

遺伝要因と環境要因の調査

目次

第1章 概要

第2章 調査手法

第3章 エグゼクティブサマリー

第4章 顧客の声

第5章 世界の特発性肺線維症市場展望

• 市場規模・予測
  • 金額別
• 市場シェア・予測
  • 薬剤の種類別（ピルフェニドン、ニンテダニブ、その他）
  • 投与経路別（非経口、経口、その他）
  • 流通チャネル別（病院薬局、小売薬局、オンライン薬局）
  • 地域別
  • 企業別（2024）
• 市場マップ

第6章 北米の特発性肺線維症市場展望

• 市場規模・予測
• 市場シェア・予測
• 北米：国別分析
  • 米国
  • カナダ
  • メキシコ

第7章 欧州の特発性肺線維症市場展望

• 市場規模・予測
• 市場シェア・予測
• 欧州：国別分析
  • ドイツ
  • 英国
  • イタリア
  • フランス
  • スペイン

第8章 アジア太平洋地域の特発性肺線維症市場展望

• 市場規模・予測
• 市場シェア・予測
• アジア太平洋地域：国別分析
  • 中国
  • インド
  • 日本
  • 韓国
  • オーストラリア

第9章 南米の特発性肺線維症市場展望

• 市場規模・予測
• 市場シェア・予測
• 南米：国別分析
  • ブラジル
  • アルゼンチン
  • コロンビア

第10章 中東・アフリカの特発性肺線維症市場展望

• 市場規模・予測
• 市場シェア・予測
• 中東・アフリカ：国別分析
  • 南アフリカ
  • サウジアラビア
  • アラブ首長国連邦

第11章 市場力学

• 促進要因
• 課題

第12章 市場動向と発展

• 合併と買収（ある場合）
• 製品の発売（ある場合）
• 最近の動向

第13章 ポーターのファイブフォース分析

• 業界内の競合
• 新規参入の可能性
• サプライヤーの力
• 顧客の力
• 代替品の脅威

第14章 競合情勢

• Boehringer Ingelheim International GmbH
• F. Hoffmann-La Roche Ltd.
• Cipla Limited
• Shionogi & Co., Ltd
• Bristol-Myers Squibb Company
• United Therapeutics Corporation
• FibroGen, Inc
• Pliant Therapeutics, Inc
• Galecto, Inc.
• CSL Behring

第15章 戦略的提言

第16章 調査会社について・免責事項

lobal Idiopathic Pulmonary Fibrosis Market was valued at USD 3.64 Billion in 2024 and is expected to reach USD 5.39 Billion by 2030 with a CAGR of 6.72% during the forecast period. The lung condition idiopathic pulmonary fibrosis (IPF) is dangerous. When you breathe in, oxygen enters your bloodstream through small air sacs in your lungs. It then makes its way to your inside organs. Epidemiological data from Prescriber, published in July 2022, indicates that the annual incidence of idiopathic pulmonary fibrosis in Europe ranges from 0.22 to 7.4 cases per 100,000 individuals, with approximately 32,500 cases reported in the United Kingdom alone.

Your lungs get congested with scar tissue because of IPF. With time, it becomes worse. Like the scars you receive on your skin after a cut, the IPF scar tissue is dense. It inhibits the transfer of oxygen from your lungs to your blood, which might prevent your body from functioning properly. Idiopathic pulmonary fibrosis can exist for a very long time without any symptoms showing up. When someone is exposed to anything like pollution, certain medications, or an illness, they may develop pulmonary fibrosis. Doctors are unsure of what causes IPF, though.

Diagnosing IPF involves a combination of medical history, physical examination, lung function tests, high-resolution computed tomography (HRCT) scans, and, in some cases, a lung biopsy. IPF is often challenging to diagnose because its symptoms can overlap with those of other lung diseases. Improved diagnostic techniques, such as high-resolution computed tomography (HRCT) and the identification of biomarkers, have enabled earlier and more accurate detection of IPF. This has increased the number of patients seeking treatment. The ongoing research and development of new drugs and therapies for IPF have led to the introduction of novel treatments, which expand the available options for patients. The approval of innovative therapies is a driving force in the market. Increased awareness campaigns and educational initiatives about IPF symptoms and the importance of early diagnosis have resulted in more patients seeking medical care. Healthcare professionals are also better equipped to recognize the disease. The focus on patient-centered care, including support groups, patient advocacy, and improving the quality of life for IPF patients, has become a driving factor in the market. Patient advocacy organizations play a crucial role in raising awareness and improving patient care.

Key Market Drivers

Advancements in Diagnosis

High-Resolution Computed Tomography (HRCT) imaging has become a gold standard in diagnosing IPF. It provides detailed images of the lungs, allowing healthcare professionals to detect characteristic patterns of fibrosis. HRCT is non-invasive and has significantly improved the accuracy of IPF diagnosis. Ongoing research into biomarkers, such as specific proteins or genetic markers, has the potential to aid in early diagnosis and disease monitoring. Identifying biomarkers associated with IPF can help distinguish it from other lung conditions. Minimally invasive lung biopsy techniques, such as transbronchial cryobiopsy and endobronchial ultrasound-guided biopsy, offer alternatives to traditional surgical biopsies. These techniques provide tissue samples for analysis, aiding in the confirmation of IPF diagnosis.

Multi-Disciplinary Discussion (MDD) approach involves a team of specialists, including radiologists, pulmonologists, and pathologists, who jointly evaluate patient data, imaging, and biopsy results. This collaborative approach enhances the accuracy of IPF diagnosis. AI and machine learning algorithms have been applied to HRCT scans and other patient data to improve diagnostic accuracy. These technologies can assist in identifying patterns and characteristics of IPF that may be missed by human observers. Telemedicine has become a valuable tool, especially during the COVID-19 pandemic. It allows healthcare professionals to remotely assess patients, review diagnostic images, and provide consultation for individuals in remote or underserved areas. Genetic testing for specific gene mutations associated with familial IPF can help confirm the diagnosis in cases where a family history of the disease is present. International guidelines and consensus statements, such as those from the American Thoracic Society (ATS) and the European Respiratory Society (ERS), have provided standardized criteria for diagnosing IPF, facilitating consistency in diagnosis. Improved understanding of the clinical presentation and symptoms of IPF has enabled healthcare providers to diagnose the disease more accurately. Common symptoms include progressive breathlessness and dry cough. Bronchoalveolar Lavage (BAL) is a diagnostic procedure that involves collecting fluid from the air sacs in the lungs. It can help rule out other lung diseases and contribute to the diagnostic process. This factor will help in the development of the Global Idiopathic Pulmonary Fibrosis Market.

Key Market Challenges

High Cost of Treatment

Idiopathic Pulmonary Fibrosis (IPF) is a chronic and often progressive disease that requires long-term treatment. The high cost of medications, therapy, and healthcare services can impose a substantial financial burden on patients and their families, potentially leading to financial stress. Some IPF treatments, especially newer and more advanced therapies, may not be fully covered by health insurance plans. This can result in out-of-pocket expenses for patients, making it difficult for them to access necessary treatments. The high cost of IPF treatment can create disparities in access to care. Patients with limited financial resources may face barriers to accessing the most effective therapies, leading to disparities in outcomes. The cost of treatment can impact patients' adherence to prescribed medications and therapies. Patients may reduce or skip doses due to cost concerns, which can affect the effectiveness of the treatment. The high cost of IPF treatment places a financial burden on healthcare systems and insurance providers, potentially limiting the availability of certain treatments or leading to increased healthcare costs for society. High treatment costs can lead to financial toxicity, which has a negative impact on patients' overall well-being. This can include increased stress, anxiety, and reduced quality of life. Pharmaceutical companies face significant research and development costs when developing new IPF treatments. The high cost of development and regulatory approval can contribute to the high prices of these therapies once they reach the market. High costs can lead some patients to discontinue or delay their treatment, which may result in disease progression and more severe health outcomes.

Key Market Trends

Research into Genetic and Environmental Factors

Research into genetic factors helps identify individuals who may be at a higher risk of developing IPF. This knowledge can lead to personalized screening and preventative strategies. Genetic and environmental research may reveal biomarkers that can be used for early detection and diagnosis of IPF, enabling healthcare providers to intervene at an earlier, potentially more treatable stage of the disease. Identifying genetic and environmental risk factors allows for risk assessment and counseling for individuals with a family history of IPF or who have been exposed to certain environmental triggers.

Genetic research can help identify specific pathways and mechanisms underlying IPF. This knowledge may lead to the development of targeted therapies that address the root causes of the disease. Understanding the genetic and environmental factors contributing to an individual's IPF can inform the development of personalized treatment plans, optimizing therapy for each patient's unique needs. Research into environmental factors, such as exposure to certain toxins or pollutants, can help identify strategies for reducing exposure and preventing the development or exacerbation of IPF. Patients with IPF may benefit from genetic counseling to understand the hereditary aspects of the disease, particularly in cases of familial IPF. Insights gained from genetic and environmental research can uncover novel therapeutic targets, which may lead to the development of innovative treatments for IPF.

Segmental Insights

Distribution Channel Insights

In 2024, the Global Idiopathic Pulmonary Fibrosis Market largest share was held by hospital pharmacies segment in the forecast period and is predicted to continue expanding over the coming years. In some regions, a significant proportion of IPF patients receive treatment on an inpatient basis, particularly during acute exacerbations or advanced stages of the disease. Hospital pharmacies are responsible for dispensing and managing medications for these inpatients. Hospitals often play a key role in conducting clinical trials for new IPF treatments. The distribution and management of trial medications may involve hospital pharmacies. IPF treatment can involve complex medication regimens, including the use of oxygen therapy, immunosuppressive drugs, and other specialized medications. Hospital pharmacies are equipped to handle these complex regimens. Regional healthcare regulations and reimbursement policies can influence the distribution of medications. In some cases, regulations or policies may favour or require hospital-based distribution of certain medications.

Key Market Players

• Boehringer Ingelheim International GmbH
• F. Hoffmann-La Roche Ltd.
• Cipla Limited
• Shionogi & Co., Ltd
• Bristol-Myers Squibb Company
• United Therapeutics Corporation
• FibroGen, Inc
• Pliant Therapeutics, Inc
• Galecto, Inc.
• CSL Behring

Report Scope:

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

Idiopathic Pulmonary Fibrosis Market, By Drug Type:

• Pirfenidone
• Nintedanib
• others
• Idiopathic Pulmonary Fibrosis Market, By Route of Administration
• Oral
• Parenteral
• Others

Idiopathic Pulmonary Fibrosis Market, By Distribution Channel:

• Hospital Pharmacies
• Retail Pharmacies
• Online Pharmacies

Idiopathic Pulmonary Fibrosis Market, By region:

• North America
  • United States
  • Canada
  • Mexico
• Asia-Pacific
  • China
  • India
  • South Korea
  • Australia
  • Japan
• Europe
  • Germany
  • France
  • United Kingdom
  • Spain
  • Italy
• South America
  • Brazil
  • Argentina
  • Colombia
• Middle East & Africa
  • South Africa
  • Saudi Arabia
  • UAE

Competitive Landscape

Company Profiles: Detailed analysis of the major companies presents in the Global Idiopathic Pulmonary Fibrosis Market.

Available Customizations:

Global Idiopathic Pulmonary Fibrosis 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

• Detailed analysis and profiling of additional market players (up to five).

Table of Contents

1. Product Overview

• 1.1. Market Definition
• 1.2. Scope of the Market
  • 1.2.1. Markets Covered
  • 1.2.2. Years Considered for Study
  • 1.2.3. Key Market Segmentations

2. Research Methodology

• 2.1. Objective of the Study
• 2.2. Baseline Methodology
• 2.3. Key Industry Partners
• 2.4. Major Association and Secondary Sources
• 2.5. Forecasting Methodology
• 2.6. Data Triangulation & Validations
• 2.7. Assumptions and Limitations

3. Executive Summary

• 3.1. Overview of the Market
• 3.2. Overview of Key Market Segmentations
• 3.3. Overview of Key Market Players
• 3.4. Overview of Key Regions/Countries
• 3.5. Overview of Market Drivers, Challenges, Trends

4. Voice of Customer

5. Global Idiopathic Pulmonary Fibrosis Market Outlook

• 5.1. Market Size & Forecast
  • 5.1.1. By Value
• 5.2. Market Share & Forecast
  • 5.2.1. By Drug Type (Pirfenidone, Nintedanib, others)
  • 5.2.2. By Route of Administration (Parenteral, Oral, Others)
  • 5.2.3. By Distribution Channel (Hospital Pharmacies, Retail Pharmacies, Online Pharmacies)
  • 5.2.4. By Region
  • 5.2.5. By Company (2024)
• 5.3. Market Map

6. North America Idiopathic Pulmonary Fibrosis Market Outlook

• 6.1. Market Size & Forecast
  • 6.1.1. By Value
• 6.2. Market Share & Forecast
  • 6.2.1. By Drug Type
  • 6.2.2. By Route of Administration
  • 6.2.3. By Distribution Channel
  • 6.2.4. By Country
• 6.3. North America: Country Analysis
  • 6.3.1. United States Idiopathic Pulmonary Fibrosis Market Outlook
    • 6.3.1.1. Market Size & Forecast
      • 6.3.1.1.1. By Value
    • 6.3.1.2. Market Share & Forecast
      • 6.3.1.2.1. By Drug Type
      • 6.3.1.2.2. By Route of Administration
      • 6.3.1.2.3. By Distribution Channel
  • 6.3.2. Canada Idiopathic Pulmonary Fibrosis Market Outlook
    • 6.3.2.1. Market Size & Forecast
      • 6.3.2.1.1. By Value
    • 6.3.2.2. Market Share & Forecast
      • 6.3.2.2.1. By Drug Type
      • 6.3.2.2.2. By Route of Administration
      • 6.3.2.2.3. By Distribution Channel
  • 6.3.3. Mexico Idiopathic Pulmonary Fibrosis Market Outlook
    • 6.3.3.1. Market Size & Forecast
      • 6.3.3.1.1. By Value
    • 6.3.3.2. Market Share & Forecast
      • 6.3.3.2.1. By Drug Type
      • 6.3.3.2.2. By Route of Administration
      • 6.3.3.2.3. By Distribution Channel

7. Europe Idiopathic Pulmonary Fibrosis Market Outlook

• 7.1. Market Size & Forecast
  • 7.1.1. By Value
• 7.2. Market Share & Forecast
  • 7.2.1. By Drug Type
  • 7.2.2. By Route of Administration
  • 7.2.3. By Distribution Channel
  • 7.2.4. By Country
• 7.3. Europe: Country Analysis
  • 7.3.1. Germany Idiopathic Pulmonary Fibrosis Market Outlook
    • 7.3.1.1. Market Size & Forecast
      • 7.3.1.1.1. By Value
    • 7.3.1.2. Market Share & Forecast
      • 7.3.1.2.1. By Drug Type
      • 7.3.1.2.2. By Route of Administration
      • 7.3.1.2.3. By Distribution Channel
  • 7.3.2. United Kingdom Idiopathic Pulmonary Fibrosis Market Outlook
    • 7.3.2.1. Market Size & Forecast
      • 7.3.2.1.1. By Value
    • 7.3.2.2. Market Share & Forecast
      • 7.3.2.2.1. By Drug Type
      • 7.3.2.2.2. By Route Of Administration
      • 7.3.2.2.3. By Distribution Channel
  • 7.3.3. Italy Idiopathic Pulmonary Fibrosis Market Outlook
    • 7.3.3.1. Market Size & Forecast
      • 7.3.3.1.1. By Value
    • 7.3.3.2. Market Share & Forecast
      • 7.3.3.2.1. By Drug Type
      • 7.3.3.2.2. By Route Of Administration
      • 7.3.3.2.3. By Distribution Channel
  • 7.3.4. France Idiopathic Pulmonary Fibrosis Market Outlook
    • 7.3.4.1. Market Size & Forecast
      • 7.3.4.1.1. By Value
    • 7.3.4.2. Market Share & Forecast
      • 7.3.4.2.1. By Drug Type
      • 7.3.4.2.2. By Route Of Administration
      • 7.3.4.2.3. By Distribution Channel
  • 7.3.5. Spain Idiopathic Pulmonary Fibrosis Market Outlook
    • 7.3.5.1. Market Size & Forecast
      • 7.3.5.1.1. By Value
    • 7.3.5.2. Market Share & Forecast
      • 7.3.5.2.1. By Drug Type
      • 7.3.5.2.2. By Route Of Administration
      • 7.3.5.2.3. By Distribution Channel

8. Asia-Pacific Idiopathic Pulmonary Fibrosis Market Outlook

• 8.1. Market Size & Forecast
  • 8.1.1. By Value
• 8.2. Market Share & Forecast
  • 8.2.1. By Drug Type
  • 8.2.2. By Route Of Administration
  • 8.2.3. By Distribution Channel
  • 8.2.4. By Country
• 8.3. Asia-Pacific: Country Analysis
  • 8.3.1. China Idiopathic Pulmonary Fibrosis Market Outlook
    • 8.3.1.1. Market Size & Forecast
      • 8.3.1.1.1. By Value
    • 8.3.1.2. Market Share & Forecast
      • 8.3.1.2.1. By Drug Type
      • 8.3.1.2.2. By Route Of Administration
      • 8.3.1.2.3. By Distribution Channel
  • 8.3.2. India Idiopathic Pulmonary Fibrosis Market Outlook
    • 8.3.2.1. Market Size & Forecast
      • 8.3.2.1.1. By Value
    • 8.3.2.2. Market Share & Forecast
      • 8.3.2.2.1. By Drug Type
      • 8.3.2.2.2. By Route Of Administration
      • 8.3.2.2.3. By Distribution Channel
  • 8.3.3. Japan Idiopathic Pulmonary Fibrosis Market Outlook
    • 8.3.3.1. Market Size & Forecast
      • 8.3.3.1.1. By Value
    • 8.3.3.2. Market Share & Forecast
      • 8.3.3.2.1. By Drug Type
      • 8.3.3.2.2. By Route Of Administration
      • 8.3.3.2.3. By Distribution Channel
  • 8.3.4. South Korea Idiopathic Pulmonary Fibrosis Market Outlook
    • 8.3.4.1. Market Size & Forecast
      • 8.3.4.1.1. By Value
    • 8.3.4.2. Market Share & Forecast
      • 8.3.4.2.1. By Drug Type
      • 8.3.4.2.2. By Route Of Administration
      • 8.3.4.2.3. By Distribution Channel
  • 8.3.5. Australia Idiopathic Pulmonary Fibrosis Market Outlook
    • 8.3.5.1. Market Size & Forecast
      • 8.3.5.1.1. By Value
    • 8.3.5.2. Market Share & Forecast
      • 8.3.5.2.1. By Drug Type
      • 8.3.5.2.2. By Route Of Administration
      • 8.3.5.2.3. By Distribution Channel

9. South America Idiopathic Pulmonary Fibrosis Market Outlook

• 9.1. Market Size & Forecast
  • 9.1.1. By Value
• 9.2. Market Share & Forecast
  • 9.2.1. By Drug Type
  • 9.2.2. By Route Of Administration
  • 9.2.3. By Distribution Channel
  • 9.2.4. By Country
• 9.3. South America: Country Analysis
  • 9.3.1. Brazil Idiopathic Pulmonary Fibrosis Market Outlook
    • 9.3.1.1. Market Size & Forecast
      • 9.3.1.1.1. By Value
    • 9.3.1.2. Market Share & Forecast
      • 9.3.1.2.1. By Drug Type
      • 9.3.1.2.2. By Route Of Administration
      • 9.3.1.2.3. By Distribution Channel
  • 9.3.2. Argentina Idiopathic Pulmonary Fibrosis Market Outlook
    • 9.3.2.1. Market Size & Forecast
      • 9.3.2.1.1. By Value
    • 9.3.2.2. Market Share & Forecast
      • 9.3.2.2.1. By Drug Type
      • 9.3.2.2.2. By Route of Administration
      • 9.3.2.2.3. By Distribution Channel
  • 9.3.3. Colombia Idiopathic Pulmonary Fibrosis Market Outlook
    • 9.3.3.1. Market Size & Forecast
      • 9.3.3.1.1. By Value
    • 9.3.3.2. Market Share & Forecast
      • 9.3.3.2.1. By Drug Type
      • 9.3.3.2.2. By Route of Administration
      • 9.3.3.2.3. By Distribution Channel

10. Middle East and Africa Idiopathic Pulmonary Fibrosis Market Outlook

• 10.1. Market Size & Forecast
  • 10.1.1. By Value
• 10.2. Market Share & Forecast
  • 10.2.1. By Drug Type
  • 10.2.2. By Route Of Administration
  • 10.2.3. By Distribution Channel
  • 10.2.4. By Country
• 10.3. MEA: Country Analysis
  • 10.3.1. South Africa Idiopathic Pulmonary Fibrosis Market Outlook
    • 10.3.1.1. Market Size & Forecast
      • 10.3.1.1.1. By Value
    • 10.3.1.2. Market Share & Forecast
      • 10.3.1.2.1. By Drug Type
      • 10.3.1.2.2. By Route Of Administration
      • 10.3.1.2.3. By Distribution Channel
  • 10.3.2. Saudi Arabia Idiopathic Pulmonary Fibrosis Market Outlook
    • 10.3.2.1. Market Size & Forecast
      • 10.3.2.1.1. By Value
    • 10.3.2.2. Market Share & Forecast
      • 10.3.2.2.1. By Drug Type
      • 10.3.2.2.2. By Route Of Administration
      • 10.3.2.2.3. By Distribution Channel
  • 10.3.3. UAE Idiopathic Pulmonary Fibrosis Market Outlook
    • 10.3.3.1. Market Size & Forecast
      • 10.3.3.1.1. By Value
    • 10.3.3.2. Market Share & Forecast
      • 10.3.3.2.1. By Drug Type
      • 10.3.3.2.2. By Route Of Administration
      • 10.3.3.2.3. By Distribution Channel

11. Market Dynamics

• 11.1. Drivers
• 11.2. Challenges

12. Market Trends & Developments

• 12.1. Merger & Acquisition (If Any)
• 12.2. Product Launches (If Any)
• 12.3. Recent Developments

13. Porter's Five Forces Analysis

• 13.1. Competition in the Industry
• 13.2. Potential of New Entrants
• 13.3. Power of Suppliers
• 13.4. Power of Customers
• 13.5. Threat of Substitute Products

14. Competitive Landscape

• 14.1. Boehringer Ingelheim International GmbH
  • 14.1.1. Business Overview
  • 14.1.2. Company Snapshot
  • 14.1.3. Products & Services
  • 14.1.4. Financials (As Reported)
  • 14.1.5. Recent Developments
  • 14.1.6. Key Personnel Details
  • 14.1.7. SWOT Analysis
• 14.2. F. Hoffmann-La Roche Ltd.
• 14.3. Cipla Limited
• 14.4. Shionogi & Co., Ltd
• 14.5. Bristol-Myers Squibb Company
• 14.6. United Therapeutics Corporation
• 14.7. FibroGen, Inc
• 14.8. Pliant Therapeutics, Inc
• 14.9. Galecto, Inc.
• 14.10. CSL Behring

15. Strategic Recommendations

16. About Us & Disclaimer