Gilead Sciences, Inc. today announced that the European Commission (EC) has granted conditional marketing authorization for seladelpar for the treatment of primary biliary cholangitis (PBC) in ...

Ipsen has been given accelerated approval by the FDA for Iqirvo, which becomes the first dual PPAR alpha/delta agonist for rare cholestatic liver disease primary biliary cholangitis (PBC).

Gilead acquired Livdelzi – an oral PPAR delta agonist – as the main asset in its $4.3 billion takeover of CymaBay Therapeutics in February. Prior to that, it was in development for metabolic ...

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