Prognia
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🇪🇺EU · EMAAuthorisedATC: L01BB07

Atriance(nelarabine)

Precursor T-Cell Lymphoblastic Leukemia-Lymphoma

Marketing Authorisation Holder: Sandoz Pharmaceuticals d.d.

EMA Authorisation: 22/08/2007

INN: nelarabine

Indication

Nelarabine is indicated for the treatment of patients with T-cell acute lymphoblastic leukaemia (T-ALL) and T-cell lymphoblastic lymphoma (T-LBL) whose disease has not responded to or has relapsed following treatment with at least two chemotherapy regimens. Due to the small patient populations in these disease settings, the information to support these indications is based on limited data.

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.