Intercept Pharmaceuticals

18 total trials 1 currently recruiting 12 completed

Intercept Pharmaceuticals sponsors 18 registered US clinical trials on ClinicalTrials.gov, 1 of them currently recruiting, and 12 completed. 6 of these trials are in Phase 3-4 (later-stage) and 11 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Alcohol-associated Hepatitis, with 1 trials.

Trial Pipeline

18 total, page 1 of 1

RECRUITING Phase 2

FXR Effect on Severe Alcohol-Associated Hepatitis (FRESH) Study

NCT05639543

TERMINATED Phase 3

To Evaluate Safety and Tolerability of the Fixed- Dose Combination of Obeticholic Acid and Bezafibrate

NCT06488911

COMPLETED Phase 2

Study of OCA in Combination With BZF Evaluating Efficacy, Safety and Tolerability in Participants With PBC

NCT05239468

TERMINATED Phase 4

Study of Obeticholic Acid (OCA) Evaluating Pharmacokinetics and Safety in Participants With Primary Biliary Cholangitis (PBC) and Hepatic Impairment

NCT03633227

COMPLETED Phase 3

Study Evaluating the Efficacy and Safety of Obeticholic Acid in Subjects With Compensated Cirrhosis Due to Nonalcoholic Steatohepatitis

NCT03439254

COMPLETED Phase 2

Combination Obeticholic Acid (OCA) and Statins for Monitoring of Lipids (CONTROL)

NCT02633956

TERMINATED Phase 3

Randomized Global Phase 3 Study to Evaluate the Impact on NASH With Fibrosis of Obeticholic Acid Treatment

NCT02548351

COMPLETED

Real-World Data Study to Evaluate the Effectiveness of OCA on Hepatic Outcomes in PBC Patients

NCT05292872

COMPLETED Phase 2

Obeticholic Acid (OCA) in Primary Sclerosing Cholangitis (PSC)

NCT02177136

TERMINATED Phase 4

Phase 4 Study of Obeticholic Acid Evaluating Clinical Outcomes in Patients With Primary Biliary Cholangitis

NCT02308111

COMPLETED Phase 2

Phase 2 Study on Effects of Obeticholic Acid (OCA) on Lipoprotein Metabolism in Participants With Primary Biliary Cirrhosis

NCT01865812

COMPLETED Phase 1

Single Dose and Multiple Dose Trial to Assess Pharmacokinetics of Obeticholic Acid (OCA)

NCT01933503

COMPLETED Phase 1

Effect of Food on Pharmacokinetics of Obeticholic Acid (OCA)

NCT01914562

COMPLETED Phase 1

Hepatic Impairment Trial of Obeticholic Acid

NCT01904539

COMPLETED Phase 3

Phase 3 Study of Obeticholic Acid in Patients With Primary Biliary Cirrhosis

NCT01473524

COMPLETED Phase 2

Study of INT-747 as Monotherapy in Participants With Primary Biliary Cirrhosis (PBC)

NCT00570765

TERMINATED Phase 2

Study of INT 747 in Combination With URSO in Patients With Primay Biliary Cirrhosis (PBC)

NCT00550862

COMPLETED Phase 2

Study of INT-747 in Patients With Diabetes and Presumed NAFLD

NCT00501592

Phase Distribution

PhaseTrial count
Phase 1 3
Phase 2 8
Phase 3 4
Phase 4 2

Therapeutic Areas

What the Pipeline for Intercept Pharmaceuticals Shows

According to the ClinicalTrials.gov registry, Intercept Pharmaceuticals is linked to 18 US clinical trials across every stage of research activity. Of those, 1 studies are currently recruiting, about 6% of the sponsor's indexed portfolio, and 12 are already marked complete, representing roughly 67% of the total.

The phase mix for Intercept Pharmaceuticals reports 6 late-stage studies (Phase 3 and Phase 4 combined) and 11 earlier-phase studies (Phase 1 and Phase 2).

The top therapeutic focus area indexed for Intercept Pharmaceuticals is Alcohol-associated Hepatitis with 1 linked trial, and 0 other condition areas appear in the top list above.

How to read these pipeline numbers

Recruiting share is one of the more practical signals here: it reflects how much of a sponsor's research is presently open to new participants, while the completed share indicates the depth of finished work that has already contributed registry results. Both counts come directly from the public ClinicalTrials.gov dataset and are refreshed on the registry side; this page mirrors the latest data pull without altering it.

A portfolio weighted toward Phase 3 usually reflects an organization advancing candidates toward regulatory review, where the research centers on comparative efficacy and broader safety across larger populations. A heavier Phase 1 and Phase 2 tilt generally indicates exploratory work, safety, dosing, and early signal detection, and is common among research-forward sponsors that seed many early programs. Phase 4 entries, when present, track interventions already in real-world use and typically focus on long-term safety, effectiveness across subgroups, or formulation comparisons.

That distribution is a quick read of where the organization concentrates its research attention; it does not imply product availability, market share, or any clinical endorsement. All numbers on this page come from ClinicalTrials.gov maintained by the National Library of Medicine, and counts can shift as new studies are registered or existing ones update their status. This information is provided for reference and educational purposes only, not as medical, investment, or regulatory advice, verify current details directly with ClinicalTrials.gov before relying on any figure here.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page aggregates every registered trial from this sponsor, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.