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

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however, the rates were low and adequately mitigated or managed with low- or high-dose buprenorphine induction

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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