Viewing Study NCT00337727



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Last Modification Date: 2024-10-26 @ 9:25 AM
Study NCT ID: NCT00337727
Status: COMPLETED
Last Update Posted: 2017-06-02
First Post: 2006-06-14

Brief Title: Aprepitant for the Prevention of Chemotherapy Induced Nausea and Vomiting CINV0869-130COMPLETED
Sponsor: Merck Sharp Dohme LLC
Organization: Merck Sharp Dohme LLC

Study Overview

Official Title: A Randomized Double-Blind Parallel-Group Study Conducted Under In-House Blinding Conditions to Determine the Efficacy and Tolerability of Aprepitant for the Prevention of Chemotherapy Induced Nausea and Vomiting CINV Associated With Moderately Emetogenic Chemotherapy MEC
Status: COMPLETED
Status Verified Date: 2017-05
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The study will test aprepitant for the prevention of CINV in patients receiving their initial cycle of Moderately Emetogenic Chemotherapy MEC Patients receiving more then one cycle of chemotherapy may opt to participate in an optional second cycle during which the patient will receive the same antiemetic regimen as cycle 1 except that an IV formulation of aprepitant will be given in place of the oral formulation on study day one Study drug administration on subsequent days will be given orally as in cycle 1
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
2006_016 OTHER protocol number None