Code: MTA8434 | Publication Date: Sep 2025 |
The market is expanding rapidly as obesity, type 2 diabetes, and sedentary lifestyles contribute to rising disease prevalence, while pharmaceutical advancements accelerate development of targeted therapies for liver inflammation and fibrosis.
The Non-Alcoholic Steatohepatitis Market is witnessing notable trends centered on personalized medicine, companion diagnostics, and combination therapies. Companies in the biopharmaceutical space focus on molecules that can target inflammation, fibrosis, and lipid metabolism that address the underlying mechanisms of the disease.
Trends also include utilization of artificial intelligence for early diagnosis, collaborations between diagnostic and pharma companies, and increasing interest in RNA-based therapies. Public-private partnerships and collaborations between industry and academia will continue to facilitate innovation and development.
The Non-Alcoholic Steatohepatitis Market is seeing developments in fibrosis-targeting agents, metabolic modulators, and immune pathway inhibitors. FGF21 analogs, ACC inhibitors, and inhibitors of thyroid hormone receptor-β are currently being evaluated by drug developers associating them with possible new therapeutic avenues for treating liver disease.
Advances in non-invasive diagnostics, intended to lower reliance on the liver biopsy are also gaining traction. New clinical pipelines, orphan drug designations, and predictive analytics also show opportunities for companies to gain a competitive edge and reduce time-to-market.
Below is a comprehensive list of the leading market players driving growth in this sector:
Company Name | Intercept Pharmaceuticals |
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Established Year | 2002 |
Headquarters | Morristown, United States |
Official Website | Click Here |
Intercept is known for developing obeticholic acid (OCA), a therapy candidate targeting liver fibrosis in NASH patients.
Company Name | Madrigal Pharmaceuticals |
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Established Year | 2011 |
Headquarters | West Conshohocken, United States |
Official Website | Click Here |
Madrigal is advancing MGL-3196 (Resmetirom), a selective thyroid hormone receptor-β agonist for NASH treatment.
Company Name | Gilead Sciences |
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Established Year | 1987 |
Headquarters | Foster City, United States |
Official Website | Click Here |
Gilead is developing multiple NASH candidates, including FGF21 analogs and FXR agonists for anti-fibrotic treatment.
Company Name | Galmed Pharmaceuticals |
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Established Year | 2000 |
Headquarters | Tel Aviv, Israel |
Official Website | Click Here |
Galmed is working on Aramchol, a liver-targeted drug modulating lipid metabolism and inflammation in NASH.
Company Name | Genfit |
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Established Year | 1999 |
Headquarters | Lille, France |
Official Website | Click Here |
Genfit is focused on NASH diagnostics and therapeutics, including elafibranor and biomarker-based testing.
Company Name | Akero Therapeutics |
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Established Year | 2017 |
Headquarters | South San Francisco, United States |
Official Website | Click Here |
Akero is advancing Efruxifermin, an FGF21 analog designed to improve insulin sensitivity and reduce liver fat.
Company Name | 89bio Inc. |
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Established Year | 2018 |
Headquarters | San Francisco, United States |
Official Website | Click Here |
89bio develops biologic therapies for NASH, including pegozafermin targeting metabolic and fibrotic pathways.
Company Name | Terns Pharmaceuticals |
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Established Year | 2017 |
Headquarters | Foster City, United States |
Official Website | Click Here |
Terns is building a pipeline of monotherapies and combination treatments for NASH and related liver diseases.
Company Name | Sagimet Biosciences |
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Established Year | 2006 |
Headquarters | San Mateo, United States |
Official Website | Click Here |
Sagimet is focused on fatty acid synthase inhibitors to treat underlying metabolic drivers of NASH.
Company Name | Pfizer Inc. |
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Established Year | 1849 |
Headquarters | New York, United States |
Official Website | Click Here |
Pfizer is pursuing strategic partnerships and NASH-specific programs targeting metabolic dysfunction and liver fibrosis.