PBC drug combo safety check ends early
NCT ID NCT06488911
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at the long-term safety of a fixed-dose combination of two drugs (obeticholic acid and bezafibrate) for people with primary biliary cholangitis (PBC), a chronic liver disease. It enrolled 62 adults who had already been taking the combination in earlier studies. The study was terminated early, and its main goal was to track side effects, serious side effects, and changes in lab results. Because PBC requires ongoing treatment, this is classified as disease control, not a cure.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Academisch Medisch Centrum
Amsterdam, 1005 AZ, Netherlands
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Akershus University Hospital
Lørenskog, 1478, Norway
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American Research Corporation
San Antonio, Texas, 78215, United States
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Artroscan s.r.o. Gastroenterologicka
Ostrava, 722100, Czechia
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Azienda Ospedaliero-Universitaria di Bologna Policlinico S. Orsola-Malpighi
Bologna, Italy
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Beth Israel Deaconess Medical Center
Boston, Massachusetts, 02215, United States
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CHRU de Lille
Lille, 59000, France
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CHU Paris Est - Hopital Saint Antoine
Paris, 75012, France
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Consorcio Hospital General Universitario
Valencia, 46014, Spain
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DEOEC II. sz. Belgygyszati Klinika
Debrecen, 4032, Hungary
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DIM Clinica Privada
Buenos Aires, Argentina
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East Tennessee Research Institute
Johnson City, Tennessee, 37604, United States
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Ege University, Faculty of Medicine, Gastroenterology
Bornova, Turkey (Türkiye)
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Flinders Medical Centre
Bedford Park, 5042, Australia
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Gastro One
Germantown, Tennessee, 38138, United States
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Hacettepe University, Faculty of Medicine, Adult Hospital Gastroenterology
Ankara, Turkey (Türkiye)
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Hadassah Ein-Karem Medical Center - Liver unit
Jerusalem, 9112001, Israel
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Harran University Hospital, Gastroenterology
Sanliurfa, Turkey (Türkiye)
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Hepato-Gastroenterologie HK, s.r.o.
Hradec Králové, 50012, Czechia
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Hopital Henri Mondor
Créteil, 94000, France
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Hopital de la Pitie Salpetriere
Paris, 75013, France
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Hospital ClinicUniversity of Barcelona
Barcelona, 8036, Spain
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Hospital Italiano de Buenos Aires
Buenos Aires, Argentina
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Hospital Italiano de La Plata
Buenos Aires, Argentina
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Hospital Provincial del Centenario
Santa Fe, Argentina
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Hospital Universitario Austral
Buenos Aires, Argentina
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Houston Methodist Hospital
Houston, Texas, 77030, United States
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Hull University Teaching Hospitals NHS Trust
Hull, HU32JZ, United Kingdom
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Institute of Cellular Medicine Newcastle University
Newcastle upon Tyne, NE7 7DN, United Kingdom
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Istanbul University, Capa Faculty of Medicine, Gastroenterology
Istanbul, Turkey (Türkiye)
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John Radcliffe Hospital
Oxford, OX3 9DU, United Kingdom
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Kyungpook National University Hospital
Daegu, 41944, South Korea
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Medizinische Hochschule Hannover
Hanover, 30625, Germany
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NYU Langone Health
New York, New York, 10016, United States
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Ochsner Clinic Foundation
New Orleans, Louisiana, 70121, United States
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Pacific Gastroenterology Associates GI Research Institute
Vancouver, British Columbia, Canada
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Piedmont Atlanta Hospital
Atlanta, Georgia, 30309, United States
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Research Site SRO
Pilsen, 30100, Czechia
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Royal Adelaide Hospital
Adelaide, 5000, Australia
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Seoul National University Bundang Hospital
Seongnam-si, 463-707, South Korea
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Southern California Research Center
Coronado, California, 92118, United States
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Tampa General Medical Group
Tampa, Florida, 33606, United States
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Tartu University Hospital
Tartu, 50090, Estonia
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The Liver Institute at Methodist Dallas Medical Center
Dallas, Texas, 75203, United States
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UZ Leuven
Leuven, 3000, Belgium
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University Hopital Santaros klinikos
Vilnius, 8661, Lithuania
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University Hospital of Larissa
Larissa, 41110, Greece
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University Hospitals Cleveland Medical Center
Cleveland, Ohio, 44106, United States
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University of Alabama at Birmingham
Birmingham, Alabama, 35233, United States
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University of Alberta Division of Gastroenterology Zeidler Ledcor Centre
Edmonton, Alberta, Canada
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Universityl Hospital Dubrava
Zagreb, 10 000, Croatia
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Other studies related to the condition(s) this trial covers.
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