Clinical Trials Logo

Clinical Trial Summary

This study aims to demonstrate that, when given concomitantly with a 5-hydroxytryptamine 3 (5-HT3) antagonist and a corticosteroid, a single 150 mg intravenous (IV) dose of fosaprepitant given on Day 1 is superior to the control regimen of 5-HT3 antagonist and corticosteroid only, in preventing chemotherapy-induced nausea and vomiting (CINV) associated with moderately emetogenic chemotherapy (MEC).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01594749
Study type Interventional
Source Merck Sharp & Dohme Corp.
Contact
Status Completed
Phase Phase 3
Start date September 24, 2012
Completion date November 3, 2014

See also
  Status Clinical Trial Phase
Not yet recruiting NCT04912271 - Granisetron Transdermal Patch for Prophylaxis of Delayed CINV Phase 3
Active, not recruiting NCT05434663 - Safety Study of Repeat Doses of SUSTOL in Adults Phase 4
Recruiting NCT04472143 - Granisetron Transdermal Patch for Prophylaxis of Nausea and Vomiting in Patients Receiving Oral Anticancer Agents Phase 2
Completed NCT00619359 - Evaluation of Fosaprepitant (MK0517) in Single Dose Schedule (0517-017) Phase 3
Completed NCT03204279 - PK/PD Study of Netupitant and Palonosetron in Pediatric Patients for Prevention of Chemotherapy-induced Nausea and Vomiting Phase 2
Completed NCT00952341 - Aprepitant/MK0869 for Prevention of Chemotherapy Induced Nausea and Vomiting Associated With Cisplatin (0869-169)(COMPLETED) Phase 3
Completed NCT01111851 - Aprepitant and Fosaprepitant Time-on-Target PET (Positron Emission Tomography) Study (0869-183) Phase 1