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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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    Combination therapy with adalimumab plus low-dose methotrexate induced a two-fold reduction of treatment failure among pediatric patients with Crohn’s disease, according to research published in Gastroenterology. “Tumor necrosis factor inhibitors (TNFi), including infliximab and adalimumab, are a mainstay of pediatric Crohn’s disease therapy; however, non-response and loss of

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    • #ICYMI from @AGA_Gastro: “The #evaluation and #comparison of additional strategies to further optimize response to #adalimumab, including proactive therapeutic #drug monitoring, warrant additional research," @MichaelKappel12 told @GoHealio #GI. https://t.co/ouFO1V0tdh