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EMA Product

Pixuvri

Product approved by European Medicines Agency (EU)

Basic Information

Pixuvri

Regulatory Information

EMEA/H/C/002055

Expired

May 10, 2012

February 16, 2012

23

December 7, 2021

Company Information

France

Les Laboratoires Servier 50 rue Carnot F-92284 Suresnes Cedex

LES LABORATOIRES SERVIER

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Pixuvri is indicated as monotherapy for the treatment of adult patients with multiply relapsed or refractory aggressive non-Hodgkin B-cell lymphomas (NHL). The benefit of pixantrone treatment has not been established in patients when used as fifth-line or greater chemotherapy in patients who are refractory to last therapy.

Overview Summary

This is a summary of the European public assessment report (EPAR) for Pixuvri. It explains how the Committee for Medicinal Products for Human Use (CHMP) assessed the medicine to reach its opinion in favour of granting a marketing authorisation and its recommendations on the conditions of use for Pixuvri.

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