Genfit believes elafibranor’s clean tolerability and safety profile may help narrow the gap between it and Intercept’s OCA, with safety questions delaying OCA’s entry to market. Part two of Scrip’s interview with Genfit’s CEO and COO.
Genfit SA is positioned to bring the second drug to market in non-alcoholic steatohepatitis (NASH) behind Intercept Pharmaceuticals Inc.’s obeticholic acid (OCA), but some analysts have expressed little confidence in Genfit’s elafibranor because of initially poor data in a Phase II trial. New Genfit CEO Pascal Prigent and his team are fighting against that perception as they look forward to reporting data from the Phase III RESOLVE-IT trial early in 2020.
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