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Primary Biliary Cholangitis Treatment Market Driven by Novel Therapeutics and Increasing Diagnostic Accuracy | Intercept Pharmaceuticals, Inc., Gilead Sciences, Inc., Ipsen Biopharmaceuticals, Inc., Teva Pharmaceuticals USA, Inc.

07-28-2025 09:59 AM CET | Health & Medicine

Press release from: DataM intelligence 4 Market Research LLP

Primary Biliary Cholangitis Treatment Market

Primary Biliary Cholangitis Treatment Market

The Global Primary Biliary Cholangitis Treatment Market reached US$ 1.33 billion in 2024 and is expected to reach US$ 2.72 billion by 2033, growing at a CAGR of 7.8 % during the forecast period of 2025-2033.

Primary Biliary Cholangitis Treatment Market Report by DataM Intelligence offers a detailed assessment of the global pharmaceutical and healthcare landscape, highlighting market size, key players, and critical growth drivers. With a focus on emerging drug technologies, evolving treatment paradigms, and regulatory frameworks, the report delivers strategic insights to support stakeholders in navigating the rapidly advancing sector from 2025 to 2033.

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PBC is a chronic autoimmune liver disease that damages bile ducts. The market is growing with approved therapies like ursodeoxycholic acid (UDCA) and obeticholic acid. Pipeline interest is strong, with novel agents targeting FXR receptors, fibrosis, and inflammation gaining traction.

Primary Biliary Cholangitis Treatment Market Competitors Overview:

Intercept Pharmaceuticals, Inc., Gilead Sciences, Inc., Ipsen Biopharmaceuticals, Inc., Teva Pharmaceuticals USA, Inc., Glenmark Pharmaceuticals Inc., AbbVie Inc., Aden Healthcare., Zydus Therapeutics Inc., COUR Pharmaceuticals, Kowa Company, Ltd., Mirum Pharma, Parvus Therapeutics Inc, GSK plc., Strides Pharma Science Limited, and Calliditas Therapeutics AB. Among others.

Important Industry Updates of 2024 and 2025:

✅ In February 2025, Gilead Sciences, Inc. announced that the European Commission (EC) had granted conditional marketing authorization for seladelpar for the treatment of Primary Biliary Cholangitis (PBC). This approval allows the use of seladelpar in combination with ursodeoxycholic acid (UDCA) for adults who have had an inadequate response to UDCA alone, or as a monotherapy for those who cannot tolerate UDCA.

Methodology and Scope

The Primary Biliary Cholangitis Treatment Market Report is built on a rigorous research methodology that integrates primary interviews, expert insights, and validated secondary data from company reports, industry publications, and reliable databases. Utilizing both bottom-up and top-down approaches, the analysis ensures high data accuracy through triangulation. The report covers current market dynamics, growth opportunities, and key strategic developments across global and regional markets.

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Primary Biliary Cholangitis Treatment Market Segments Overview:

∎ By Drug Type (Obeticholic Acid, Seladelpar, Elafibranor, Ursodeoxycholic Acid (UDCA), Others)
∎ By Age Group (Adults, Geriatrics)

Regional Overview for Primary Biliary Cholangitis Treatment Market:

⇥ North America (U.S., Canada, Mexico)
⇥ Europe (U.K., Italy, Germany, Russia, France, Spain, The Netherlands and Rest of Europe)
⇥ Asia-Pacific (India, Japan, China, South Korea, Australia, Indonesia Rest of Asia Pacific)
⇥ South America (Colombia, Brazil, Argentina, Rest of South America)
⇥ Middle East & Africa (Saudi Arabia, U.A.E., South Africa, Rest of Middle East & Africa)

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The Report Covers:

➡ In-depth analysis of the demand-supply gap, market size estimates, SWOT and PESTEL analysis, along with global market forecasts.
➡ Strategic recommendations with a focused go-to-market approach.
➡ An unbiased evaluation of overall market performance.
➡ Region- and country-specific insights, with customized reports available upon request.
➡ Identification of high-potential and niche segments and regions demonstrating strong growth prospects.

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