European Commission Approves BYANNLI® (6-monthly Paliperidone Palmitate; PP6M) for the Maintenance Treatment of Schizophrenia in Adults

PRESS RELEASE

03/12/2021

Janssen Global Services, LLC

BEERSE, BELGIUM, 23 November, 2021 – The Janssen Pharmaceutical Companies of Johnson & Johnson today announced the approval of the long-acting atypical antipsychotic therapy BYANNLI® (6-monthly paliperidone palmitate; PP6M) by the European Commission (EC) for the maintenance treatment of schizophrenia in adult patients who are clinically stable on 1-monthly paliperidone palmitate (PP1M) or 3-monthly paliperidone palmitate (PP3M).1 The approval makes PP6M the first twice-yearly treatment for adults living with schizophrenia to be approved by the EC, with the longest available dosing interval for an antipsychotic medication in the European Economic Area.

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