Idiopathic Pulmonary Fibrosis Market is estimated to be valued at USD 4,950 Mn in 2025 and is expected to reach USD 8,875.9 Mn in 2032, exhibiting a compound annual growth rate (CAGR) of 8.7% from 2025 to 2032.
Aging populations, rising awareness, and increasing disease prevalence are steadily expanding the idiopathic pulmonary fibrosis (IPF) market. Approved antifibrotic drugs like pirfenidone and nintedanib continue to support treatment adoption, while the growing availability of generics enhances affordability. Ongoing clinical trials for innovative therapies, along with favorable reimbursement policies and improved diagnostic technologies, are further accelerating the idiopathic pulmonary fibrosis market growth.
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Pirfenidone acquired the prominent share of 50.5% in 2025. Pirfenidone propels the IPF market by delaying disease progression and preserving lung function, backed by strong clinical evidence and its early approval as one of the first licensed antifibrotics. Its early market entry and global regulatory approvals helped build a strong reputation. The launch of generic versions has lowered its cost, while ongoing research—focusing on combination therapies and sustained-release formulations—continues to drive its rapid growth. For instance, in May 2022, Sandoz, a global leader in generic and biosimilar medicines, has announced the U.S. launch of its generic pirfenidone, the first AB-rated (fully substitutable) equivalent to Genentech's Esbriet®*, for treating idiopathic pulmonary fibrosis (IPF). The prescription oral medication is now available through specialty pharmacies, with a $0 co-pay program for eligible patients. This is further accelerating the idiopathic pulmonary fibrosis market demand.
Oral medicines dominate the IPF market by offering convenient at-home dosing that supports long-term adherence. Antifibrotic drugs like pirfenidone and nintedanib gain widespread use due to strong clinical outcomes and simple dosing regimens. The introduction of generics has reduced costs, while enhanced reimbursement policies have improved access. Advancements in imaging enable earlier diagnosis, allowing patients to start treatment sooner, and ongoing R&D into new oral drugs and formulations continues to drive market growth. For instance, in September 2024, Trevi Therapeutics, Inc., a clinical-stage biopharmaceutical company, developed Haduvio™ (oral nalbuphine ER) as an investigational therapy to treat chronic cough associated with idiopathic pulmonary fibrosis (IPF) and refractory chronic cough (RCC). This is further propelling the idiopathic pulmonary fibrosis market revenue.
Hospital pharmacies control acquires the most prominent share in 2025 by dispensing antifibrotics and specialty medications during inpatient stays, especially for acute exacerbations and complex treatment regimens. They ensure accurate dosing, maintain pharmacovigilance, and integrate closely with diagnostic and patient monitoring systems. Hospital settings also support clinical trials for investigational IPF therapies, emphasizing the crucial role these pharmacies play in initiating treatment and delivering advanced care.

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North America leads the global IPF market with a share of 37.80% by leveraging strong R&D efforts, high patient awareness, and advanced healthcare infrastructure. The region ensures widespread availability of antifibrotic drugs like pirfenidone and nintedanib through robust diagnostic systems and favorable reimbursement policies. Canada contributes to this momentum by expanding diagnostic capabilities and maintaining universal healthcare coverage.
The Asia Pacific region is experiencing the fastest growth in the global IPF market as countries improve diagnosis, increase healthcare spending, and raise disease awareness. Governments are advancing early detection and treatment adoption through national health programs, particularly in urban centers with advanced medical infrastructure. Nations like China, India, and Indonesia are expanding access to specialized care and investing heavily in diagnostic tools like high-resolution CT scanners and pulmonary function labs to enable accurate, early IPF detection. For instance, in June 2025, Specialized Therapeutics (ST) announced the extension of its existing supply and distribution agreement with Incyte Biosciences International Sàrl, the Swiss affiliate of Incyte. Under the expanded agreement, ST will introduce and distribute two additional oncology drugs in Australia, New Zealand, and Singapore, with the potential to include more Asia-Pacific countries.
Major cities like Beijing, Shanghai, and Guangzhou have enhanced early and accurate IPF diagnosis by upgrading pulmonary labs, specialized clinics, and HRCT capabilities. However, primary and rural hospitals continue to face shortages of imaging equipment and trained radiologists. Chinese regulatory authorities approved pirfenidone and nintedanib, transforming IPF treatment. Domestic manufacturers have introduced cost-effective generics, improving accessibility and affordability across urban and peri-urban regions. Domestic drug development and licensing deals, such as the Bersiporocin agreement, highlight China’s growing pharmaceutical ecosystem. For instance, in February 2025, Cumberland Pharmaceuticals Inc. and SciClone Pharmaceuticals (Holdings) Limited announced that the NMPA has approved Cumberland's Vibativ® injection in China. This is further propelling the idiopathic pulmonary fibrosis market revenue.
Advancements in U.S. healthcare have enabled the widespread use of HRCT scans, pulmonary labs, and specialized facilities, allowing for early and accurate IPF diagnosis. This infrastructure strengthens IPF management and ensures timely initiation of antifibrotic treatments. Favorable insurance coverage, especially through Medicare, improves access to costly IPF drugs. Ongoing investments in clinics and healthcare systems further support market stability by ensuring continuous treatment delivery and patient care. For instance, in May 2023, Cumberland Pharmaceuticals, a U.S.-based company, unveiled the Phase II FIGHTING FIBROSIS trial of oral ifetroban for idiopathic pulmonary fibrosis (IPF). This move follows the U.S. Food and Drug Administration’s approval of the company’s investigational new drug application for the treatment.
| Report Coverage | Details | ||
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| Base Year: | 2024 | Market Size in 2025: | USD 4,950 Mn |
| Historical Data for: | 2020 To 2024 | Forecast Period: | 2025 To 2032 |
| Forecast Period 2025 to 2032 CAGR: | 8.7% | 2032 Value Projection: | USD 8,875.9 Mn |
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| Companies covered: |
Genentech, Inc., Boehringer Ingelheim International GmbH, Avalyn Pharma, Inc., AstraZeneca, Blade Therapeutics, Bristol-Myers Squibb Company, Cipla Inc., F. Hoffmann-La Roche, FibroGen, Inc., Galapagos NV, MediciNova, Inc., Merck & Co., Inc., Promedior, Inc., Prometic Life Sciences Inc., Daewoong Pharmaceutical (India) Pvt Ltd, Sandoz International GmbH (Novartis) and Algernon Pharmaceuticals Inc. |
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The global increase in IPF cases is closely tied to aging populations and exposure to risk factors such as smoking, air pollution, and occupational hazards. As more individuals reach the 60+ age group, IPF diagnoses continue to rise. This trend is especially pronounced in developed regions like North America, Europe, and parts of Asia. Increased disease awareness, coupled with improved diagnostic capabilities, also contributes to the detection of more cases, thereby expanding the treatment market.
Emerging markets offer a strong growth opportunity through the expansion of diagnostic infrastructure. Early and accurate diagnosis of IPF remains a challenge in low- and middle-income countries due to limited access to HRCT and pulmonary specialists. Companies that provide affordable diagnostic tools, AI-based imaging analysis, or telehealth-supported respiratory assessments can play a key role in these markets. Improved diagnosis will enable earlier treatment initiation, ultimately expand the eligible treatment population and boost long-term market revenues.
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About Author
Ghanshyam Shrivastava - With over 20 years of experience in the management consulting and research, Ghanshyam Shrivastava serves as a Principal Consultant, bringing extensive expertise in biologics and biosimilars. His primary expertise lies in areas such as market entry and expansion strategy, competitive intelligence, and strategic transformation across diversified portfolio of various drugs used for different therapeutic category and APIs. He excels at identifying key challenges faced by clients and providing robust solutions to enhance their strategic decision-making capabilities. His comprehensive understanding of the market ensures valuable contributions to research reports and business decisions.
Ghanshyam is a sought-after speaker at industry conferences and contributes to various publications on pharma industry.
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