Woman and Man
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Extract
Efficacy: To compare the single IV dose of fosaprepitant (in combination with ondansetron) to the ondansetron alone regimen with respect to the efficacy endpoint of Complete Response in the delayed phase (>24 to 120 hours) following the initiation of emetogenic chemotherapy in Cycle 1. Safety: To assess the safety and tolerability of the fosaprepitant regimen in pediatric subjects who are receiving emetogenic chemotherapy.
Inclusion criteria
- Chemotherapy-induced nausea and vomiting (CINV) associated with emetogenic chemotherapy