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Providers must track which payer covers which service types to avoid crossover claim denials

Disclosure of interest: Trevor Wendt: nothing to disclose

The supplemental approval is based on data from the Phase III PhALLCON trial, in which treatment with Iclusig led to superior MRD-negative complete remission rates and had comparable safety to Novartis Gleevec in adults with newly diagnosed Ph+ ALL

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It is the percentage of the API absorbed through non-intravenous administration compared with the corresponding same medicine administered intravenously