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Clinical Trial Summary

The primary objective of this study is to compare the absorption of a prepared aprepitant oral suspension with that of the aprepitant capsule in children being treated with chemotherapy agents that are likely to cause vomiting.


Clinical Trial Description

Antiemetic therapies have improved in recent years, but chemotherapy-induced nausea and vomiting (CINV) are still common and are among the most distressing side effects of chemotherapy. In a recent survey, parents of children receiving chemotherapy in Ontario centres identified nausea as the fourth most prevalent and bothersome treatment-related symptom experienced by their children. Aprepitant is commercially available in Canada as capsules. An oral liquid aprepitant formulation would be ideal for oral administration to children. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01249001
Study type Interventional
Source The Hospital for Sick Children
Contact
Status Terminated
Phase Phase 2
Start date October 2010
Completion date September 28, 2016

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