Clinical Trials Logo

Clinical Trial Summary

The purpose of this study is to examine the safety, tolerability, and efficacy of MK0517 to prevent Chemotherapy-Induced Nausea and Vomiting (CINV) associated with Cisplatin chemotherapy.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Prevention


Related Conditions & MeSH terms


NCT number NCT00619359
Study type Interventional
Source Merck Sharp & Dohme Corp.
Contact
Status Completed
Phase Phase 3
Start date February 2008
Completion date June 2009

See also
  Status Clinical Trial Phase
Completed NCT01594749 - Efficacy and Safety of Fosaprepitant Dimeglumine in Preventing Chemotherapy-Induced Nausea and Vomiting (MK-0517-031) Phase 3
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 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