Further Erleada approval in Europe

29 January 2020

The European Commission (EC) has approved a second indication in prostate cancer for Erleada (apalutamide), from the Johnson & Johnson (NYSE: JNJ) unit Janssen.

This second indication is for the treatment of adult men with metastatic hormone-sensitive prostate cancer (mHSPC), in combination with androgen deprivation therapy (ADT), a group of patients who currently number more than 100,000 across Europe.

Previously, Erleada was approved in Europe for use in adults with non-metastatic castration-resistant prostate cancer (nmCRPC) who are at high risk of developing metastatic disease.

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