Intercept Pharmaceuticals
Manufacturing · New Jersey, United States · 201-500 Employees
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Overview
Headquarters
305 Madison Ave, Morristown, New Jersey,...Phone Number
(646) 747-1000Website
www.interceptpharma.comRevenue
$101.3 MillionIndustry
About Intercept Pharmaceuticals
Intercept Pharmaceuticals Org Chart
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Intercept Pharmaceuticals is experiencing very low activity levels compared to other companies in the Manufacturing sector.
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Intercept Pharmaceuticals is drawing exceptional interest within the Manufacturing industry, suggesting notable developments or strong market momentum, learn more about Intercept Pharmaceuticals.
Intercept Pharmaceuticals financials insights
Gather financial insights about Intercept Pharmaceuticals, including details on funding rounds, investors, total funding, and acquisitions, to gain a comprehensive understanding of their financial strategy.
Series B
$25M
Series C
$30M
Stock Offering
$75M
Stock Offering
$61.7M
Stock Offering
$183.3M
Debt
$447.7M
Stock Offering
$250M
Stock Offering
$200M
Debt
$210.4M
Intercept Pharmaceuticals Tech Stack
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Intercept Pharmaceuticals News & Media
Intercept Announces Voluntary Withdrawal of OCALIVA® for Primary Biliary Cholangitis (PBC) from the US Market; US Clinical Trials Involving Obeticholic Acid Placed on Clinical Hold
MORRISTOWN, N.J., Sept. 11, 2025 (GLOBE NEWSWIRE) -- Intercept Pharmaceuticals, Inc., a wholly owned biopharmaceutical subsidiary of Alfasigma S.p.A., today announced its decision to voluntarily withdraw OCALIVA® (obeticholic acid) from the US market for the treatment of primary biliary cholangitis (PBC), a rare, progressive liver disease. This decision follows a request from the US Food and Drug Administration (FDA). In addition, FDA has placed a clinical hold on all Intercept clinical trials cIntercept Announces Data to be Presented at Digestive Disease Week 2025
Abstracts include a presidential plenary-selected Phase 2 study evaluating the combination of obeticholic acid and bezafibrate in PBC, along with 10 other abstracts Abstracts include a presidential plenary-selected Phase 2 study evaluating the combination of obeticholic acid and bezafibrate in PBC, along with 10 other abstractsIntercept Receives Complete Response Letter from FDA Addressing OCALIVA supplemental New Drug Application (sNDA)
MORRISTOWN, N.J., Nov. 12, 2024 (GLOBE NEWSWIRE) -- Intercept Pharmaceuticals, Inc., a wholly owned biopharmaceutical subsidiary of Alfasigma S.p.A., today announced that the U.S. Food and Drug Administration (FDA) has issued a Complete Response Letter (CRL) that addresses the supplemental New Drug Application (sNDA) for OCALIVA® (obeticholic acid, OCA) seeking full approval for the treatment of indicated patients with primary biliary cholangitis (PBC) – a rare, progressive disease that dispropoIntercept Provides Regulatory Update Regarding sNDA for OCALIVA
MORRISTOWN, N.J., Oct. 17, 2024 (GLOBE NEWSWIRE) -- Intercept Pharmaceuticals, Inc., a wholly owned subsidiary of Alfasigma S.p.A., today announced that the U.S. Food and Drug Administration (FDA) has informed the Company that it is continuing its review of the supplemental New Drug Application (sNDA) for full approval of OCALIVA® (obeticholic acid, OCA) for the treatment of indicated patients with primary biliary cholangitis (PBC), and its action under the Prescription Drug User Fee Act (PDUFA)
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Frequently Asked Questions Regarding Intercept Pharmaceuticals
Intercept Pharmaceuticals operates as a biopharmaceutical company specializing in the development and commercialization of therapeutics targeting liver diseases. The company focuses on addressing significant unmet medical needs within hepatology through targeted drug development and clinical research initiatives. By concentrating its efforts on liv... Read More