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EMA Product

Atriance

Product approved by European Medicines Agency (EU)

Basic Information

Atriance

Regulatory Information

EMEA/H/C/000752

Authorised

August 22, 2007

29

July 26, 2024

Company Information

Slovenia

Verovškova ulica 57 1000 Ljubljana

SANDOZ PHARMACEUTICALS D.D.

Drug Classification

Additional MonitoringExceptional Circumstances

Active Ingredients

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic 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.

Overview Summary

Atriance is a cancer medicine used to treat patients with T-cell acute lymphoblastic leukaemia (T-ALL) or T-cell lymphoblastic lymphoma (T-LBL). These are types of cancer where T-lymphoblasts (a type of immature white blood cell) multiply too quickly. In T-ALL the abnormal cells are mainly in the blood and bone marrow, and in T-LBL they are mainly in the lymphatic system (lymph nodes or thymus gland). Atriance is used when the cancer has not responded to, or has stopped responding to, at least two types of chemotherapy. Atriance contains the active substance nelarabine.

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