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Fibrotic diseases treatment market seen reaching $58.1 billion by 2035

8 hours ago
By AI, Created 12:16 UTC, Sep 17, 2026, AGP -

Market Research Future projects the global fibrotic diseases treatment market will more than double to $58.1 billion by 2035 from $27.4 billion in 2025, driven by rising disease burden, more clinical readouts and expanding metabolic liver disease care. North America leads revenue now, while Asia-Pacific is expected to grow fastest through the forecast period.

Why it matters: - The fibrotic diseases treatment market is moving from a narrow specialty area into a larger, more durable revenue pool. - Growth is being driven by more diagnosed patients, earlier detection and more drugs reaching late-stage development. - The market could matter more for payers and health systems as fibrosis care shifts from symptom management toward disease-modifying treatment.

What happened: - Market Research Future projected the global fibrotic diseases treatment market will rise from USD 27.4 billion in 2025 to USD 58.1 billion by 2035. - The forecast implies a 7.8% compound annual growth rate from 2026 to 2035. - The market was valued at USD 29.5 billion in 2026 under the report’s forecast path. - North America held 41.5% of 2025 revenue. - Asia-Pacific was forecast to be the fastest-growing region at a 9.4% CAGR through 2035. - The report was published Sept. 17, 2026.

The details: - Rising disease burden is a core growth driver. - The report cites about 50,000 new idiopathic pulmonary fibrosis diagnoses annually in the United States. - Specialist-care prevalence in Europe was measured at 36.0 per 100,000 population. - The World Health Organization attributes more than 1.3 million deaths a year to cirrhosis. - ClinicalTrials.gov listed 214 interventional fibrosis studies in active recruitment in Q4 2025, up from 118 five years earlier. - About 38% of adults in high-income economies have steatotic liver disease, and 5% to 7% of those patients progress to significant fibrosis. - Nintedanib and pirfenidone are reimbursed in 47 countries. - The U.S. FDA’s orphan-drug incentive framework has helped keep idiopathic pulmonary fibrosis programs viable despite trial attrition above 60%. - The European Commission’s Innovative Health Initiative committed EUR 2.4 billion across 2021-2027 to chronic organ-injury research. - Global venture and corporate investment in fibrosis-focused biotechs topped USD 4.1 billion from 2023 to 2025. - About 38% of that capital went to hepatic indications. - Elastography and blood-based panels cut fibrosis staging costs by an estimated 62% versus biopsy. - NHS England’s community liver-health pathway screened more than 400,000 at-risk adults from 2023 to 2025 and found advanced fibrosis in about 4.8%. - Medication was the largest treatment segment in 2025 with a 58.2% share. - Organ transplantation was valued at USD 5.9 billion in 2025. - Oxygen therapy was the fastest-growing treatment line at a 6.1% CAGR from 2026 to 2035. - Idiopathic pulmonary fibrosis was the largest application in 2025 with a 38.4% share. - Hepatic cirrhosis was valued at USD 7.6 billion in 2025. - Renal fibrosis was the fastest-growing application at a 9.1% CAGR from 2026 to 2035. - Hospitals led end-user revenue with a 62.5% share in 2025. - Academic and research institutes accounted for USD 6.5 billion in 2025. - North America’s market was led by the United States, which generated about 86.4% of regional revenue. - Europe’s market was led by Germany, which held 23.8% of regional revenue. - China held 38.6% of Asia-Pacific revenue. - India was the fastest-growing Asia-Pacific market at an 11.2% CAGR. - Brazil anchored South America with 58.3% of regional revenue. - Saudi Arabia held 31.5% of Middle East and Africa revenue.

Between the lines: - The report suggests fibrosis is becoming a broader commercial category because diagnostics are pulling patients into care earlier. - Hepatic fibrosis is emerging as a major growth engine because screening programs are expanding the addressable population before severe disease develops. - The competitive market remains concentrated, but not enough to shut out newer entrants in liver and kidney fibrosis. - The top five players held about 47% of 2025 revenue, leaving room for contestable segments. - Combination regimens, biomarker-based trials and machine-learning staging tools could reshape treatment and trial economics over the next decade. - Boehringer Ingelheim reported positive Phase III results for nerandomilast in September 2024, strengthening the case for a new pulmonary mechanism. - Madrigal Pharmaceuticals secured accelerated FDA approval for resmetirom in March 2024, creating the first reimbursed pharmacological pathway for hepatic fibrosis. - Gilead Sciences entered a hepatic antifibrotic licensing deal in April 2025, showing larger drugmakers are still moving into the space.

What's next: - The report expects more readouts from fibrosis drug pipelines through 2035. - Eight sponsors are now running Phase II trials that combine an established antifibrotic backbone with an integrin or autotaxin inhibitor. - Asia-Pacific access should keep widening as reimbursement expands in China and generic manufacturing scales in India. - The report says first human proof-of-concept studies for reversal approaches could read out before 2030. - By 2035, fibrosis care is expected to move further from symptom control toward disease modification and possible reversal.

The bottom line: - Fibrosis treatment is becoming a larger global market because more patients are being found earlier and more therapies are nearing commercial reality.

Disclaimer: This article was produced by AGP Wire with the assistance of artificial intelligence based on original source content and has been refined to improve clarity, structure, and readability. This content is provided on an “as is” basis. While care has been taken in its preparation, it may contain inaccuracies or omissions, and readers should consult the original source and independently verify key information where appropriate. This content is for informational purposes only and does not constitute legal, financial, investment, or other professional advice.

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