Intercept Pharmaceuticals, Inc. is getting ready once again – after a roughly three-year interruption – for commercialization of potentially the first approved non-alcoholic steatohepatitis (NASH) drug, as the user fee date for obeticholic acid (OCA) approaches. The company expects a US Food and Drug Administration advisory committee review of its new drug application a few weeks before the 22 June action date and told shareholders on 2 March that it thinks marketing of OCA in primary biliary cholangitis (PBC) will give it a head start on reaching the right clinicians in NASH.
Meanwhile, the other company with near-term likelihood of bringing a NASH drug to market in the US, Madrigal Pharmaceuticals,...








