Efficacy and Safety of Elafibranor in Primary Biliary Cholangitis
Universidade Federal do Rio Grande do Sul · Hospital de Clínicas de Porto Alegre · +28 more institutions
Abstract
Primary biliary cholangitis is a rare, chronic cholestatic liver disease characterized by the destruction of interlobular bile ducts, leading to cholestasis and liver fibrosis. Whether elafibranor, an oral, dual peroxisome proliferator-activated receptor (PPAR) α and δ agonist, may have benefit as a treatment for primary biliary cholangitis is unknown.
In this multinational, phase 3, double-blind, placebo-controlled trial, we randomly assigned (in a 2:1 ratio) patients with primary biliary cholangitis who had had an inadequate response to or unacceptable side effects with ursodeoxycholic acid to receive once-daily elafibranor, at a dose of 80 mg, or placebo. The primary end point was a biochemical response (defined as an alkaline phosphatase level of
Citation impact
- FWCI
- 46.47
- Percentile
- 100%
- References
- 33
Authors
31- KVKris V. KowdleyCorresponding
Universidade Federal do Rio Grande do Sul, Hospital de Clínicas de Porto Alegre, Liver Institute Northwest
- CLChristopher L. Bowlus
Universidade Federal do Rio Grande do Sul, Hospital de Clínicas de Porto Alegre, University of California, Davis
- CLCynthia Levy
Universidade Federal do Rio Grande do Sul, University of Miami, Hospital de Clínicas de Porto Alegre
- USUlus Salih Akarca
Universidade Federal do Rio Grande do Sul, Ege University, Hospital de Clínicas de Porto Alegre
- MRMário Reis Álvares‐da‐Silva
Universidade Federal do Rio Grande do Sul, Hospital de Clínicas de Porto Alegre
Topics & keywords
- Ursodeoxycholic acid
- Cholestasis
- Gastroenterology
- Alkaline phosphatase
- Medicine
- Internal medicine
- Placebo
- Clinical endpoint
- Good health and well-being