Idiopathic Pulmonary Fibrosis Treatment Market size was over USD 3.5 billion in 2024 and is estimated to reach USD 7.9 billion by the end of 2037, expanding at a CAGR of 7.1% during the forecast timeline, i.e., 2025-2037. In 2025, the industry size of idiopathic pulmonary fibrosis treatment is assessed at USD 3.7 billion. The market is expanding rapidly due to advancements in drug development, a growing prevalence of IPF, and increased awareness about the disease among healthcare providers. With ongoing research efforts focused on improving therapeutic efficacy and reducing side effects of current treatment, the IPF treatment market is expected to witness significant expansion in the upcoming years.
As per an article posted by the America Lung Association, dated October 2024, IPF is the most common type of pulmonary fibrosis, with nearly 25ooo new cases diagnosed each year. Most of the cases start showing symptoms between the ages of 50 and 70 years old. The article further states that even though the disease is more common among men, the number of IPF cases in women is on a significant rise. The development of combination therapies, integrating antifibrotic agents with immunomodulators is expected to gain traction. The shift toward personalized medicine, leveraging genetic and biomarker-based approaches to tailor treatment is a trend witnessed in the idiopathic pulmonary fibrosis treatment market.
Growth Drivers
Challenges
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Base Year |
2024 |
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Forecast Year |
2025-2037 |
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CAGR |
7.1% |
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Base Year Market Size (2024) |
USD 3.5 billion |
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Forecast Year Market Size (2037) |
USD 7.9 billion |
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Regional Scope |
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Route of Administration (Oral, Parenteral)
Based on the route of administration, the oral segment is projected to register a significant share in the idiopathic pulmonary fibrosis treatment market during the forecast period. This is due to its convenience, ease of use, and patient preference. Oral medications are widely used as they allow patients to manage their condition with less frequent hospital visits compared to injectable options. Additionally, oral therapies support better adherence, which is crucial in managing a chronic condition like IPF, where long-term treatment is necessary to slow disease progression. In October 2023, Bristol Mayers Squibb received U.S. FDA approval for a potential first-in-class, oral medication for people living with IPF and PPF.
End use (Hospitals and Clinics, Ambulatory Surgical Centers (ASCs), Homecare Settings)
Based on end use, hospitals and clinics segment is set to capture IPF treatment market share of over 50.6% by 2037. Hospitals play a critical part in supervising acute exacerbations of IPF and offer intensive care throughout disease progression. Meanwhile, specialty clinics offer personalized care approaches, including advanced treatments such as antifibrotic drugs and several emerging gene therapies. These healthcare facilities have the necessary resources and trained medical staff to administer complex therapies and ensure patients receive optimal care.
Our in-depth analysis of the global market includes the following segments:
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Treatment Type |
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Route of Administration |
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Age Group |
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End use |
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North America Market Analysis
North America idiopathic pulmonary fibrosis treatment market is well-established and expected to dominate the global market during the forecast period. It is majorly driven by the advanced top-quality healthcare infrastructure and significant R&D investments. The region benefits from robust government support, encouraging the development and commercialization of new IPF treatments. Collaborations between research institutions and pharmaceutical companies are expected to further bolster the market growth.
The U.S. market is expanding vastly with a high demand for advanced IPF therapies due to the relatively high prevalence of disease. The FDA’s Orphan Drug Act also encourages pharmaceutical companies to invest in IPF treatments by offering incentives for developing rare disease therapies. In May 2022, Sandoz announced the US launch of its generic pirfenidone to treat patients with IPF in the country.
Canada IPF treatment market is growing steadily majorly due to improved diagnostic capabilities. However, access to advanced therapies can be limited by cost barriers, the country’s healthcare system sometimes restricts coverage for high-cost treatments. Patient advocacy groups are advocating for more inclusive coverage and encouraging participation in clinical trials to improve the availability of IPF treatments in Canada.
APAC Market Statistics
The idiopathic pulmonary fibrosis treatment market in the APAC is expected to witness substantial growth, driven by rising respiratory disease prevalence, improving healthcare infrastructure, and increasing IPF awareness. Government support for rare disease research and expanding healthcare spending also contribute to this market’s potential. Companies are focusing on R&D in this region to cater to the growing demand for effective IPF therapies.
India market for idiopathic pulmonary fibrosis treatment is still emerging, with growth fueled by increasing awareness and better diagnostic capabilities. However, limited access to advanced therapies remains a challenge, and treatment often involves general antifibrotic and symptomatic management rather than targeted IPF-specific drugs. The local government’s further push for rare disease funding may foster further research, potentially improving the accessibility of IPF treatments in the country.
China represents a growing segment in the idiopathic pulmonary fibrosis treatment market with significant potential due to its large population and increasing incidence of respiratory diseases. The country’s healthcare reforms are focused on increasing access to innovative treatments. The China government and pharmaceutical companies are increasingly investing in clinical research and international collaborations to enhance IPF drug availability.
The companies participating in the idiopathic pulmonary fibrosis treatment market are expanding through R&D investments in new therapies, partnerships to accelerate drug discovery, and acquisitions to enhance their treatment portfolios. Many firms are also focusing on geographic expansion, particularly in emerging markets, to increase accessibility. Regulatory engagement, such as securing orphan drug status, is a key strategy to streamline approvals, while digital patient tools for patient monitoring are becoming integral to improving treatment adherence and personalized care. In September 2024, Boehringer Ingelheim released a statement that its study of nerandomilast, FIBRONEER-IPF, effectively met its primary endpoint, encouraging plans for a new drug request for IPF treatment.
Author Credits: Radhika Pawar
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