Abbott Labs pulls its MMA and BLA for psoriasis drug Ozespa
The European Medicines Agency says it has been formally notified by US Health care major Abbott Laboratories (NYSE: ABT) of its decision to withdraw its application for a centralized marketing authorization for Ozespa (briakinumab), 100mg solution for injection. The drug’s Biological License Application has also been withdrawn in the USA, Abbott said in a separate US Securities and Exchange Commission filing.
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