2020
DOI: 10.1038/s41575-020-0264-1
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Obeticholic acid for the treatment of NASH

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Cited by 12 publications
(11 citation statements)
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“…Another systemic review recommended UDCA as a frontline therapeutic option for NASH, thereby preventing its progression to cirrhosis and liver cancer [119]. Obeticholic acid: This synthetic farnesoid X receptor agonist at a dose of 25 mg daily is associated with histological improvement of NASH [120,121]. Obeticholic acid might become the first approved pharmacotherapy for NASH fibrosis after result of recent multicentre, randomized, placebo-controlled phase 3 trial done by Younossi et al [122].…”
Section: Emerging Genetic Biomarkers For Diagnosis Of Different Stagementioning
confidence: 99%
“…Another systemic review recommended UDCA as a frontline therapeutic option for NASH, thereby preventing its progression to cirrhosis and liver cancer [119]. Obeticholic acid: This synthetic farnesoid X receptor agonist at a dose of 25 mg daily is associated with histological improvement of NASH [120,121]. Obeticholic acid might become the first approved pharmacotherapy for NASH fibrosis after result of recent multicentre, randomized, placebo-controlled phase 3 trial done by Younossi et al [122].…”
Section: Emerging Genetic Biomarkers For Diagnosis Of Different Stagementioning
confidence: 99%
“…OCA leads to weight loss in patients with NASH, and weight loss caused by OCA is shown to exert additively beneficial effects on serum aminotransferase and liver histology [134]. Additionally, it significantly improves fibrosis in NASH patients [135]. It is one of the most promising drugs for treating NASH and is now in phase 3 clinical trials [136].…”
Section: Pioglitazonementioning
confidence: 99%
“…From a clinical point of view, administration of OCA in a phase II trial in NAFLD and T2DM patients resulted in an amelioration of insulin sensitivity and a decrease in liver proinflammatory markers [ 172 ]. Moreover, in a phase III clinical trial for treating NASH, the administration of 25 mg of OCA on a daily basis during 18 months improved fibrosis in NASH patients [ 173 ]. Noteworthy, some safety concerns have been raised regarding this compound such as an increased level of serum LDL cholesterol, decreased level of serum HDL cholesterol, gastrointestinal issues and pruritus.…”
Section: Therapeutic Strategiesmentioning
confidence: 99%