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Intercept Pharmaceuticals

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Namestring
Intercept Pharmaceuticals
Legal namestring
Intercept Pharmaceuticals, Inc.
Company typeenum
Private
Founded yearint
2002
Descriptiontext

Intercept Pharmaceuticals is a US-based biopharmaceutical company founded in 2002 that develops small-molecule therapeutics for rare and serious liver diseases. Its scientific platform is built on Farnesoid X Receptor (FXR) biology, a nuclear receptor pathway the company has positioned as applicable to multiple liver indications including primary biliary cholangitis (PBC), metabolic dysfunction-associated steatohepatitis (MASH), and severe alcohol-associated hepatitis. Its sole commercial product, Ocaliva (obeticholic acid) for PBC, was voluntarily withdrawn from the US market effective November 14, 2025 following FDA concerns regarding serious liver injury risks.

The company historically generated revenue through prescription drug sales of Ocaliva, distributed via specialty pharmacies with patient support services through its Interconnect program, and reached the market through enterprise field sales targeting hepatology and gastroenterology specialists. Intercept also maintained dedicated Medical Affairs functions supporting healthcare professional education and medical information requests. In 2025, Intercept was acquired by Italian biopharmaceutical company Alfasigma S.p.A. and now operates as a wholly owned subsidiary, with current strategic emphasis redirected toward advancing investigational pipeline assets derived from the FXR platform. The restructuring included a 146-employee reduction following the Ocaliva withdrawal.

Following acquisition and withdrawal of its sole commercial product, Intercept currently operates without an active revenue-generating product. Its customer base — patients with rare and serious liver diseases and the specialist physicians who treat them — is a narrow, high-acuity segment. Forward strategic direction is now contingent on pipeline progression under Alfasigma's global biopharmaceutical infrastructure, which spans more than 100 countries.

Short descriptiontext

Intercept Pharmaceuticals is a US biopharmaceutical company developing small-molecule therapeutics for rare and serious liver diseases using its Farnesoid X Receptor (FXR) biology platform. Now a wholly owned subsidiary of Alfasigma S.p.A., it is restructuring after withdrawing Ocaliva from the US market.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
501–1,000
akta.pro rankint
HeadquartersNew York, United States
HQ citystring
New York
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
liver disease therapeutics, FXR biology platform, rare disease pharmaceuticals, primary biliary cholangitis, small molecule drugs
Industry3 codes
1Gastroenterology & Hepatology Pharmaceuticals
CodeHLAIAAAIPrimaryYes
2Gastroenterology Specialty Pharmaceuticals
CodeHLAIACAEPrimaryNo
3Rare Gastroenterology & Hepatology Disorder Therapies
CodeHLAIAIALPrimaryNo
NAICS code2 codes
  • Pharmaceutical and Medicine Manufacturing32541
  • Pharmaceutical Preparation Manufacturing325412
SIC code1 code
  • Pharmaceutical Preparations2834
Product category
Specialty Biopharmaceuticals — Liver Disease Therapeutics
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model1 record
1Pharmaceutical Drug Sales
TypeOne Time License
Description

Intercept historically generated revenue through sales of prescription pharmaceutical products, specifically Ocaliva (obeticholic acid) for primary biliary cholangitis (PBC). Following the voluntary withdrawal of Ocaliva from the US market in September 2025, the company is restructuring and refocusing on developing new pipeline assets.

interceptpharma.com
Marketing channels3 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components4 values
Technology or R&D, Personnel, Marketing or Sales, Operations
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Core offering1 text field

Intercept Pharmaceuticals develops and commercializes small molecule therapeutics for rare and serious liver diseases, anchored by its proprietary Farnesoid X Receptor (FXR) biology platform. Its principal product, Ocaliva (obeticholic acid), was an FXR agonist approved for primary biliary cholangitis (PBC) in the US, but was voluntarily withdrawn from the US market in late 2025 following FDA safety concerns. The company is now restructuring and refocusing its development pipeline on additional liver disease indications, including severe alcohol-associated hepatitis and MASH/NASH.

Differentiator
Functional benefit
Problem solved
Product overview1 text field

Intercept Pharmaceuticals is a biopharmaceutical company focused on developing novel medicines for rare and serious liver diseases. The company's primary product was Ocaliva (obeticholic acid) for primary biliary cholangitis (PBC), which has been withdrawn from the market. Their research is centered on Farnesoid X Receptor (FXR) biology with potential applications across multiple liver diseases including severe alcohol-associated hepatitis. Intercept operates as a wholly owned subsidiary of Alfasigma S.p.A.

Product and service1 record
1Ocaliva (obeticholic acid)
CategoryPrescription pharmaceutical — rare liver disease therapy
Description

Ocaliva (obeticholic acid) was a prescription small molecule FXR agonist indicated for the treatment of primary biliary cholangitis (PBC) in adults, distributed through US specialty pharmacies with patient support provided by Intercept's Interconnect program. It was voluntarily withdrawn from the US market effective November 14, 2025 due to FDA safety concerns.

Scale indicator2 records

Each record includes

Type, Value, Description, Source

Partnership1 partner
Strategic tierCoreTypeOthers
Description

Intercept Pharmaceuticals was acquired by Alfasigma S.p.A. and operates as a wholly owned biopharmaceutical subsidiary. Alfasigma is a rapidly expanding global biopharmaceutical leader with presence in over 100 countries. In March 2026, Alfasigma received FDA approval for linerixibat (Lynavoy) for cholestatic pruritus in primary biliary cholangitis, licensed from GSK in a deal worth up to $690 million with $300 million upfront payment. Alfasigma is also actively involved in the Ocaliva withdrawal process and patient transition support.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight4 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Madrigal Pharmaceuticals is a direct peer focused on developing therapies for liver diseases, most notably Rezdiffra (resmetirom) for MASH. Like Intercept, Madrigal targets chronic liver disease via novel mechanisms, and both companies compete for the same hepatology/gastroenterology specialist audience and liver-focused commercial infrastructure.

TypeDirect peer
Description

Akero Therapeutics is a clinical-stage biopharmaceutical company developing efruxifermin (an FGF21 analog) for MASH and compensated liver fibrosis. It is directly comparable to Intercept as a liver-focused company pursuing novel mechanisms for serious chronic liver diseases with high unmet need.

TypeDirect peer
Description

Genfit is a France-based biopharmaceutical company with a long-standing focus on liver diseases, particularly MASH and PBC, including development of elafibranor and other candidates. It is a direct peer given its similar therapeutic area focus, public market presence, and positioning around chronic liver indications.

TypeDirect peer
Description

CymaBay Therapeutics developed seladelpar for PBC before being acquired by Gilead Sciences. It is highly comparable to Intercept as a PBC-focused specialty liver company, and both companies have pursued FXR-adjacent pathways and orphan drug strategies for rare cholestatic liver diseases.

TypeEmerging player
Description

Galectin Therapeutics is a clinical-stage company developing belapectin for liver cirrhosis and MASH. It is comparable to Intercept as a smaller, liver-focused biotech pursuing novel mechanisms for chronic fibrotic liver diseases, though it operates at an earlier stage and without Intercept's prior commercial infrastructure.

TypeEmerging player
Description

Pliant Therapeutics is a clinical-stage biotech developing integrin-based therapies for fibrotic diseases, including liver fibrosis. It overlaps with Intercept around the fibrotic liver disease space and shares a similar mechanism-driven, novel-target approach to chronic liver conditions.

TypeEmerging player
Description

NGM Biopharmaceuticals develops novel biologics for metabolic and liver diseases, including work in primary sclerosing cholangitis and other cholestatic conditions. It is an emerging peer that targets adjacent rare and serious liver indications similar to Intercept's historical PBC focus.

TypeBroad incumbent
Description

Gilead Sciences is a major biopharmaceutical company with a meaningful hepatology franchise including the CymaBay/PBC asset seladelpar and broader liver disease ambitions. It is a broad incumbent that competes with Intercept in the same liver-disease commercial channels and increasingly in the PBC therapeutic area.

TypeBroad incumbent
Description

AbbVie is a large global biopharmaceutical company with a substantial hepatology franchise and historical presence in liver-related indications. It competes for the same specialty hepatology prescribing audience and has the resources to pursue multiple liver disease programs in parallel.

TypeBroad incumbent
Description

Bristol-Myers Squibb is a large biopharmaceutical company with a strong specialty sales force that has historically been deployed in hepatology and gastroenterology. Several Intercept senior leaders (e.g., SVP of US Sales) previously held commercial leadership roles at BMS, and BMS represents the type of broad incumbent that Intercept's commercial organization was structured to compete against.

Market position
Strengths4 records

Each record includes

Headline, Details, Source

Weaknesses4 records

Each record includes

Headline, Details, Source

Competitive moat4 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Segment1 record

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile1 record

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
No
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature1 record

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles8 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds8 records

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors6 records

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Intercept Pharmaceuticals

Specialty Biopharmaceuticals — Liver Disease Therapeuticsinterceptpharma.com

Intercept Pharmaceuticals is a US biopharmaceutical company developing small-molecule therapeutics for rare and serious liver diseases using its Farnesoid X Receptor (FXR) biology platform. Now a wholly owned subsidiary of Alfasigma S.p.A., it is restructuring after withdrawing Ocaliva from the US market.

What Intercept Pharmaceuticals does

Intercept Pharmaceuticals is a US-based biopharmaceutical company founded in 2002 that develops small-molecule therapeutics for rare and serious liver diseases. Its scientific platform is built on Farnesoid X Receptor (FXR) biology, a nuclear receptor pathway the company has positioned as applicable to multiple liver indications including primary biliary cholangitis (PBC), metabolic dysfunction-associated steatohepatitis (MASH), and severe alcohol-associated hepatitis. Its sole commercial product, Ocaliva (obeticholic acid) for PBC, was voluntarily withdrawn from the US market effective November 14, 2025 following FDA concerns regarding serious liver injury risks.

The company historically generated revenue through prescription drug sales of Ocaliva, distributed via specialty pharmacies with patient support services through its Interconnect program, and reached the market through enterprise field sales targeting hepatology and gastroenterology specialists. Intercept also maintained dedicated Medical Affairs functions supporting healthcare professional education and medical information requests. In 2025, Intercept was acquired by Italian biopharmaceutical company Alfasigma S.p.A. and now operates as a wholly owned subsidiary, with current strategic emphasis redirected toward advancing investigational pipeline assets derived from the FXR platform. The restructuring included a 146-employee reduction following the Ocaliva withdrawal.

Following acquisition and withdrawal of its sole commercial product, Intercept currently operates without an active revenue-generating product. Its customer base — patients with rare and serious liver diseases and the specialist physicians who treat them — is a narrow, high-acuity segment. Forward strategic direction is now contingent on pipeline progression under Alfasigma's global biopharmaceutical infrastructure, which spans more than 100 countries.

Intercept Pharmaceuticals firmographics

Firmographics
Name
Intercept Pharmaceuticals
Legal name
Intercept Pharmaceuticals, Inc.
Website
https://interceptpharma.com
Company type
Private
Founded year
2002
Operating status
Operating
Headcount range
501–1,000 employees
Short description
Intercept Pharmaceuticals is a US biopharmaceutical company developing small-molecule therapeutics for rare and serious liver diseases using its Farnesoid X Receptor (FXR) biology platform. Now a wholly owned subsidiary of Alfasigma S.p.A., it is restructuring after withdrawing Ocaliva from the US market.
Ownership category
akta.pro rank

Intercept Pharmaceuticals industry classification

Industry
Product category
Specialty Biopharmaceuticals — Liver Disease Therapeutics
NAICS
Pharmaceutical and Medicine Manufacturing (32541), Pharmaceutical Preparation Manufacturing (325412)
SIC
Pharmaceutical Preparations (2834)
akta.pro primary industry
Gastroenterology & Hepatology Pharmaceuticals (HLAIAAAI)
akta.pro secondary industries
Gastroenterology Specialty Pharmaceuticals (HLAIACAE), Rare Gastroenterology & Hepatology Disorder Therapies (HLAIAIAL)

Keywords

  • Liver disease therapeutics
  • FXR biology platform
  • Rare disease pharmaceuticals
  • Primary biliary cholangitis
  • Small molecule drugs

Where Intercept Pharmaceuticals is headquartered

Location

Headquarters

HQ city
New York
HQ country
United States
HQ region
North America

Offices1 record

Markets served

Intercept Pharmaceuticals business model

Business model
GTM type
B2B
Offering type
Hardware or Manufacturing
Cost components
Technology or R&D, Personnel, Marketing or Sales, Operations

Revenue model

  1. Pharmaceutical Drug Sales: Intercept historically generated revenue through sales of prescription pharmaceutical products, specifically Ocaliva (obeticholic acid) for primary biliary cholangitis (PBC). Following the voluntary withdrawal of Ocaliva from the US market in September 2025, the company is restructuring and refocusing on developing new pipeline assets.

Go-to-market motion1 record

Distribution channels1 record

Marketing channels3 records

Intercept Pharmaceuticals product offering

Product offering

Core offering

Intercept Pharmaceuticals develops and commercializes small molecule therapeutics for rare and serious liver diseases, anchored by its proprietary Farnesoid X Receptor (FXR) biology platform. Its principal product, Ocaliva (obeticholic acid), was an FXR agonist approved for primary biliary cholangitis (PBC) in the US, but was voluntarily withdrawn from the US market in late 2025 following FDA safety concerns. The company is now restructuring and refocusing its development pipeline on additional liver disease indications, including severe alcohol-associated hepatitis and MASH/NASH.

Product overview

Intercept Pharmaceuticals is a biopharmaceutical company focused on developing novel medicines for rare and serious liver diseases. The company's primary product was Ocaliva (obeticholic acid) for primary biliary cholangitis (PBC), which has been withdrawn from the market. Their research is centered on Farnesoid X Receptor (FXR) biology with potential applications across multiple liver diseases including severe alcohol-associated hepatitis. Intercept operates as a wholly owned subsidiary of Alfasigma S.p.A.

Differentiator

Problem solved

Functional benefit

Products and services

  • Ocaliva (obeticholic acid) Ocaliva (obeticholic acid) was a prescription small molecule FXR agonist indicated for the treatment of primary biliary cholangitis (PBC) in adults, distributed through US specialty pharmacies with patient support provided by Intercept's Interconnect program. It was voluntarily withdrawn from the US market effective November 14, 2025 due to FDA safety concerns.

Companies that use Intercept Pharmaceuticals

Customer profile

Segments1 record

Ideal customer profiles1 record

Intercept Pharmaceuticals technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature1 record

Intercept Pharmaceuticals partnerships and signals

Strategic signal

Partnerships

One partnership is on record.

  • Alfasigma S.p.A.coreOthersIntercept Pharmaceuticals was acquired by Alfasigma S.p.A. and operates as a wholly owned biopharmaceutical subsidiary. Alfasigma is a rapidly expanding global biopharmaceutical leader with presence in over 100 countries. In March 2026, Alfasigma received FDA approval for linerixibat (Lynavoy) for cholestatic pruritus in primary biliary cholangitis, licensed from GSK in a deal worth up to $690 million with $300 million upfront payment. Alfasigma is also actively involved in the Ocaliva withdrawal process and patient transition support.

Scale indicators2 records

Recent moves6 records

Expansion highlights4 records

Intercept Pharmaceuticals competitors and assessment

Company assessment

Direct peers

  • Madrigal Pharmaceuticals: Madrigal Pharmaceuticals is a direct peer focused on developing therapies for liver diseases, most notably Rezdiffra (resmetirom) for MASH. Like Intercept, Madrigal targets chronic liver disease via novel mechanisms, and both companies compete for the same hepatology/gastroenterology specialist audience and liver-focused commercial infrastructure.
  • Akero Therapeutics: Akero Therapeutics is a clinical-stage biopharmaceutical company developing efruxifermin (an FGF21 analog) for MASH and compensated liver fibrosis. It is directly comparable to Intercept as a liver-focused company pursuing novel mechanisms for serious chronic liver diseases with high unmet need.
  • Genfit: Genfit is a France-based biopharmaceutical company with a long-standing focus on liver diseases, particularly MASH and PBC, including development of elafibranor and other candidates. It is a direct peer given its similar therapeutic area focus, public market presence, and positioning around chronic liver indications.
  • CymaBay Therapeutics: CymaBay Therapeutics developed seladelpar for PBC before being acquired by Gilead Sciences. It is highly comparable to Intercept as a PBC-focused specialty liver company, and both companies have pursued FXR-adjacent pathways and orphan drug strategies for rare cholestatic liver diseases.

Emerging players

  • Galectin Therapeutics: Galectin Therapeutics is a clinical-stage company developing belapectin for liver cirrhosis and MASH. It is comparable to Intercept as a smaller, liver-focused biotech pursuing novel mechanisms for chronic fibrotic liver diseases, though it operates at an earlier stage and without Intercept's prior commercial infrastructure.
  • Pliant Therapeutics: Pliant Therapeutics is a clinical-stage biotech developing integrin-based therapies for fibrotic diseases, including liver fibrosis. It overlaps with Intercept around the fibrotic liver disease space and shares a similar mechanism-driven, novel-target approach to chronic liver conditions.
  • NGM Biopharmaceuticals: NGM Biopharmaceuticals develops novel biologics for metabolic and liver diseases, including work in primary sclerosing cholangitis and other cholestatic conditions. It is an emerging peer that targets adjacent rare and serious liver indications similar to Intercept's historical PBC focus.

Broad incumbents

  • Gilead Sciences: Gilead Sciences is a major biopharmaceutical company with a meaningful hepatology franchise including the CymaBay/PBC asset seladelpar and broader liver disease ambitions. It is a broad incumbent that competes with Intercept in the same liver-disease commercial channels and increasingly in the PBC therapeutic area.
  • AbbVie: AbbVie is a large global biopharmaceutical company with a substantial hepatology franchise and historical presence in liver-related indications. It competes for the same specialty hepatology prescribing audience and has the resources to pursue multiple liver disease programs in parallel.
  • Bristol-Myers Squibb: Bristol-Myers Squibb is a large biopharmaceutical company with a strong specialty sales force that has historically been deployed in hepatology and gastroenterology. Several Intercept senior leaders (e.g., SVP of US Sales) previously held commercial leadership roles at BMS, and BMS represents the type of broad incumbent that Intercept's commercial organization was structured to compete against.

Market position

Strengths4 records

Weaknesses4 records

Competitive moat4 records

Key risks6 records

Customer concentration

Intercept Pharmaceuticals social profiles

Digital presence

Intercept Pharmaceuticals financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Intercept Pharmaceuticals leadership team

Management profile

Number of profiles

Profiles8 records

Intercept Pharmaceuticals funding detail

Funding detail

Funding overview

Funding rounds8 records

Investors6 records

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

Intercept Pharmaceuticals M&A and investment

M&A and investment

M&A

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about Intercept Pharmaceuticals

What does Intercept Pharmaceuticals do?

Intercept Pharmaceuticals develops and commercializes small molecule therapeutics for rare and serious liver diseases, anchored by its proprietary Farnesoid X Receptor (FXR) biology platform. Its principal product, Ocaliva (obeticholic acid), was an FXR agonist approved for primary biliary cholangitis (PBC) in the US, but was voluntarily withdrawn from the US market in late 2025 following FDA safety concerns. The company is now restructuring and refocusing its development pipeline on additional liver disease indications, including severe alcohol-associated hepatitis and MASH/NASH.

Is Intercept Pharmaceuticals a public or private company?

Intercept Pharmaceuticals is a private company. It is classified as corporate owned and is currently operating.

When was Intercept Pharmaceuticals founded?

Intercept Pharmaceuticals was founded in 2002. It employs 501 to 1,000 people.

Where is Intercept Pharmaceuticals based?

Intercept Pharmaceuticals is headquartered in New York, United States, in the North America region.

How does Intercept Pharmaceuticals make money?

One revenue line is on record: pharmaceutical Drug Sales.

Who are Intercept Pharmaceuticals's main competitors?

Direct peers on record are Madrigal Pharmaceuticals, Akero Therapeutics, Genfit and CymaBay Therapeutics. Emerging players are Galectin Therapeutics, Pliant Therapeutics and NGM Biopharmaceuticals. Broad incumbents are Gilead Sciences, AbbVie and Bristol-Myers Squibb.

Does Intercept Pharmaceuticals have an API?

No public API is recorded for Intercept Pharmaceuticals.

What industry is Intercept Pharmaceuticals in?

Intercept Pharmaceuticals's product category is Specialty Biopharmaceuticals — Liver Disease Therapeutics. Its primary akta.pro industry code is HLAIAAAI, Gastroenterology & Hepatology Pharmaceuticals, with a secondary code of HLAIACAE, Gastroenterology Specialty Pharmaceuticals. Its NAICS code is 32541 and its SIC code is 2834.

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Live signals
The Jerusalem PostUS President Donald Trump sued after attempting to sell early access to Truth postsUS President Donald Trump is facing a lawsuit filed by the Intercept and the Freedom of the Press Foundation over his Truth API service, which sells early access to posts on his Truth Social platform. The complaint, lodged in Manhattan federal court, claims that this arrangement is corrupt and undermines the integrity of financial markets, with charges as high as $100,000 a month for access to Trump's posts. The plaintiffs argue that this profit-driven model violates the First Amendment rights by restricting equal access to presidential announcements.openPR.comPrimary Biliary Cholangitis Market Outlook 2034: Growth Momentum Strengthens with Emerging Pipeline Innovations | DelveInsightDelveInsight's market report on Primary Biliary Cholangitis valued the global market at USD 1.15 billion in 2023, projecting notable growth through 2034 driven by pipeline innovations and increasing disease awareness. Key regulatory milestones include FDA accelerated approval of seladelpar (CymaBay Therapeutics) in August 2024, conditional EU approval of elafibranor by Ipsen, and a positive CHMP opinion for seladelpar from Gilead Sciences, alongside a $300 million deal in which GSK granted Alfasigma commercialization rights for linerixibat. In September 2025, Intercept Pharmaceuticals withdrew Ocaliva from the US market due to FDA concerns over serious liver injury risks, highlighting ongoing safety challenges in the PBC treatment landscape.FiercePharmaIntercept, on heels of Ocaliva withdrawal, restructures with 146 layoffsIntercept Pharmaceuticals is implementing a restructuring and cutting 146 employees in New Jersey, with layoffs starting Dec. 31 and continuing through June 30. The job cuts come three months after the company withdrew its liver disease drug Ocaliva from the U.S. market under FDA pressure, following findings that the drug's postmarketing trial "did not verify clinical benefit" and showed patients with early-stage disease had excess liver transplants and deaths. Intercept, which was acquired by Italian drugmaker Alfasigma in late 2023 after years of regulatory rejections for Ocaliva in MASH, is now focusing on INT-787, a next-generation FXR agonist being tested in a proof-of-concept study for severe alcohol-associated hepatitis.Built In NYCTop NYC, NY Biotech Companies 2025The article presents a list of biotech and life sciences companies operating in New York, New Jersey, and Pennsylvania for 2025. It provides brief organizational profiles for entities such as Kinevant Sciences, Intercept Pharmaceuticals, and C16 Biosciences, highlighting their specific therapeutic or technological focuses. The content serves as a directory rather than reporting on a specific corporate event or transaction.EIN PresswireFibrate Drugs Market Set to Reach $4.72 Billion by 2029The global fibrate drugs market is projected to grow from $3.49 billion in 2024 to $4.72 billion by 2029, driven by a compound annual growth rate of 7.2% during the forecast period, up from 2.8% historically. The anticipated growth is attributed to progressive treatment protocols, advances in precision medicine, innovation in drug delivery systems, and the rising prevalence of cardiac diseases worldwide. A key trend shaping the market is the development of fixed-dose combination drugs, exemplified by Intercept Pharmaceuticals obtaining U.S. FDA orphan drug designation in May 2023 for a combination of obeticholic acid and bezafibrate for primary biliary cholangitis treatment.EIN PresswireNorth America Metabolic Dysfunction-Associated Steatohepatitis (MASH) Treatment Market to Reach USD 17.15Bby 2033The North America MASH treatment market was valued at US$ 3.70 billion in 2024 and is projected to reach US$ 17.15 billion by 2033, growing at a CAGR of 19.3%, driven by rising obesity and diabetes prevalence and advancements in pharmacological agents targeting liver inflammation and fibrosis. Key pharmaceutical companies including Gilead Sciences, Intercept Pharmaceuticals, and Novo Nordisk are actively advancing clinical programs, with Intercept receiving FDA fast-track designation for its treatment candidate. The market is expected to benefit from increased government and private investment in clinical trials, enhanced diagnostic capabilities, and growing demand for combination therapies.ReutersIntercept Pharma pulls liver disease drug from US after regulator's requestIntercept Pharmaceuticals withdrew its liver disease drug Ocaliva from the U.S. market after the FDA requested it. The FDA had previously declined full approval and identified liver injury cases. Intercept also placed a clinical hold on all U.S. trials involving the drug.PR NewswireLeaders Come Together to Advance the Industry at Veeva SummitVeeva Systems announced its upcoming Veeva R&D and Quality Summit scheduled for September 3-4 in Boston, where leaders from multiple pharmaceutical companies including Alnylam Pharmaceuticals, BeOne Medicines, Intercept Pharmaceuticals, Merck, Pfizer, and Sanofi will share strategies on clinical, regulatory, safety, and quality advancements. Veeva will showcase AI innovations built into its Vault Platform, including Veeva AI Agents for life sciences applications. The event expects more than 2,000 attendees with over 100 sessions covering topics such as unified clinical operations, global quality management systems, and regulatory submissions.BioSpaceBiopharmas Continued Staff Cuts in 2025Several biopharmaceutical companies announced substantial workforce reductions in 2025, including Voyager Therapeutics, Intercept Pharmaceuticals, Mythic Therapeutics, and Geron. These layoffs are driven by strategic restructuring, financial pressures, and project cancellations, with ongoing impacts on their operational capacities.Market Research & Business IntelligenceNASH Drugs Pipeline Market Trends & Forecast 2025-2035The NASH (non-alcoholic steatohepatitis) drugs pipeline market is projected to grow from USD 479.7 million in 2025 to USD 8,123.3 million by 2035, representing a compound annual growth rate of 32.7%, driven by rising prevalence of obesity, diabetes, and metabolic syndrome globally. Key pharmaceutical companies including Gilead Sciences, Novo Nordisk, Intercept Pharmaceuticals, and Madrigal Pharmaceuticals are actively advancing drugs through clinical trials, with late-stage Phase III products expected to lead the pipeline landscape. Precision medicine approaches, biomarker integration, and combination therapies are identified as emerging trends that will accelerate drug development and regulatory approvals through 2035.