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🇪🇺EU · EMAWithdrawnATC: L01XC10

Arzerra(ofatumumab)

Leukemia, Lymphocytic, Chronic, B-Cell

Marketing Authorisation Holder: Novartis Europharm Ltd

EMA Authorisation: 19/04/2010

INN: ofatumumab

Indication

Previously untreated chronic lymphocytic leukaemia (CLL): Arzerra in combination with chlorambucil or bendamustine is indicated for the treatment of patients with CLL who have not received prior therapy and who are not eligible for fludarabine-based therapy. Relapsed CLL: Arzerra is indicated in combination with fludarabine and cyclophosphamide for the treatment of adult patients with relapsed CLL. Refractory CLL: Arzerra is indicated for the treatment of CLL in patients who are refractory to fludarabine and alemtuzumab.

Official EMA Resources

View on EMA (ema.europa.eu)

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Medical disclaimer: This information is intended for qualified healthcare professionals. Always verify with the official EMA Summary of Product Characteristics (SmPC) before clinical use.