Data from EMA (European Medicines Agency) - Curated by EPG Health - Last updated 16 April 2018

Indication(s)

- Tasigna 50 mg hard capsules
- Tasigna 200 mg hard capsules


Tasigna is indicated for the treatment of:
- adult and paediatric patients with newly diagnosed Philadelphia chromosome positive chronic myelogenous leukaemia (CML) in the chronic phase,
- adult patients with chronic phase and accelerated phase Philadelphia chromosome positive CML with resistance or intolerance to prior therapy including imatinib. Efficacy data in patients with CML in blast crisis are not available,
- paediatric patients with chronic phase Philadelphia chromosome positive CML with resistance or intolerance to prior therapy including imatinib.



- Tasigna 150 mg hard capsules

Tasigna is indicated for the treatment of:
- adult and paediatric patients with newly diagnosed Philadelphia chromosome positive chronic myelogenous leukaemia (CML) in the chronic phase,
- paediatric patients with Philadelphia chromosome positive CML in chronic phase with resistance or intolerance to prior therapy including imatinib.

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More information

Category Value
Agency product number EMEA/H/C/000798
Orphan designation Yes
Date First Approved 19-11-2007
Type Medicinal product subject to restricted medical prescription
Marketing authorisation holder Novartis Europharm Limited