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    The FDA granted Intercept Pharmaceuticals orphan drug designation for the fixed-dose combination of obeticholic acid and bezafibrate intended for treatment of patients with primary biliary cholangitis. Obeticholic acid (Ocaliva, Intercept Pharmaceuticals) — a farnesoid X receptor agonist — was originally FDA approved for primary biliary cholangitis (PBC) in 2016 in combination with

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    • #ICYMI: #Ocaliva plus #bezafibrate clears @US_FDA orphan #drug hurdle for primary biliary #cholangitis @InterceptPharma #GITwitter #MedTwitter https://t.co/iPpEK8qmuG

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    Patients with primary biliary cholangitis who received bezafibrate after incomplete response to Ocaliva showed lower risk for death or liver transplant, according to a presenter at the Digital International Liver Congress.“Ursodeoxycholic acid [Ocaliva, Intercept] is a first-line treatment for primary biliary cholangitis. As you know, 20% to 30% of patients exhibit incomplete response to

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    • #ILC2020: Nationwide cohort in Japan shows #bezafibrate benefits #PBC as a second-line treatment after #UDCA https://t.co/bB0pwn2IEK