Data from EMA (European Medicines Agency) - Curated by EPG Health - Last updated 28 August 2018

Indication(s)

Early breast cancer
Perjeta is indicated for use in combination with trastuzumab and chemotherapy in:
• the neoadjuvant treatment of adult patients with HER2-positive, locally advanced, inflammatory, or early stage breast cancer at high risk of recurrence
• the adjuvant treatment of adult patients with HER2-positive early breast cancer at high risk of recurrence

Metastatic breast cancer
Perjeta is indicated for use in combination with trastuzumab and docetaxel in adult patients with HER2-positive metastatic or locally recurrent unresectable breast cancer, who have not received previous anti-HER2 therapy or chemotherapy for their metastatic disease.

Full Prescribing information

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Category Value
Agency product number EMEA/H/C/002547
Orphan designation No
Date First Approved 04-03-2013
Type Medicinal product subject to restricted medical prescription
Marketing authorisation holder Roche Registration GmbH
Warnings

This medicinal product is subject to additional monitoring. This will allow quick identification of new safety information. Healthcare professionals are asked to report any suspected adverse reacti