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1           Three patients in the active-regimen group (1.0%) discontinued the study drugs owing to adverse events.
2 atment groups, 307 (71%) completed the 30-month RCT and 124 discontinued the study drug prematurely.
3                                         Two patients (0.3%) discontinued the study drugs owing to adverse events.
4                                                 One patient discontinued the study drugs owing to adverse events after we
5 hom CMV DNA was detected at a level that required treatment discontinued the study drug and received preemptive treatment

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