Active, not recruitingPhase 2NCT05627362
A Study to Assess Safety and Effectiveness of Elafibranor in Adult Participants With Primary Sclerosing Cholangitis.
Studying Primary sclerosing cholangitis
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Ipsen
- Principal Investigator
- Ipsen Medical, DirectorIpsen
- Intervention
- Elafibranor 80 mg(drug)
- Enrollment
- 68 enrolled
- Eligibility
- 18-75 years · All sexes
- Timeline
- 2022 – 2026
Study locations (30)
- Om Research LLC, Lancaster, California, United States
- Cedars-Sinai Medical Center, Los Angeles, California, United States
- University of California, Davis, Sacramento, California, United States
- Sutter Health Van Ness Campus Medical Office Building, San Francisco, California, United States
- Peak Gastroenterology Associates, Colorado Springs, Colorado, United States
- South Denver Gastroenterology,P.C., Englewood, Colorado, United States
- Rocky Mountain Gastroenterology (RMG), Littleton, Colorado, United States
- Yale University School Of Medicine - Yale Center For Clinical Investigation, New Haven, Connecticut, United States
- Schiff Center for Liver Diseases - University of Miami, Miami, Florida, United States
- Covenant Research, Sarasota, Florida, United States
- Piedmont Hospital - Piedmont Transplant Institute, Atlanta, Georgia, United States
- Tandem Clinical Research GI, Marrero, Louisiana, United States
- Mercy Medical Center, Baltimore, Maryland, United States
- Beth Israel Deaconess Medical Center, Liver Research Center, Boston, Massachusetts, United States
- Huron Gastroenterology Associates - Center for Digestive Care, Ypsilanti, Michigan, United States
- +15 more locations on ClinicalTrials.gov
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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