Drug news

EU approves Tasigna for newly diagnosed Ph+CML

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Last updated:5th Jan 2011

Published:5th Jan 2011

Source: Pharmawand

European Commission approved Tasigna (nilotinib) from Novartis for the treatment of patients with newly diagnosed Philadelphia chromosome positive chronic myeloid leukaemia (Ph+ CML) in chronic phase.A decision based on the results of the ENESTnd trial demonstrating superiority to the standard of care Glivec (imatinib) in achieving major molecular response (MMR) and complete cytogenetic response (CCyR) and delaying cancer progression.

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