Viewing Study NCT00195299



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Last Modification Date: 2024-10-26 @ 9:17 AM
Study NCT ID: NCT00195299
Status: COMPLETED
Last Update Posted: 2007-12-27
First Post: 2005-09-12

Brief Title: Study Evaluating Temsirolimus in Advanced Stage Squamous Cell Carcinoma of the Head Neck
Sponsor: Wyeth is now a wholly owned subsidiary of Pfizer
Organization: Wyeth is now a wholly owned subsidiary of Pfizer

Study Overview

Official Title: An Exploratory Biomarker Trail of Temsirolimus in Subjects With Newly Diagnosed Advanced Stage Squamous Cell Carcinoma of the Head Neck
Status: COMPLETED
Status Verified Date: 2007-12
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: This is an open-label exploratory biomarker study of intravenous temsirolimus given once weekly for 3 weeks to newly diagnosed advanced stage head and neck cancer subjects prior to beginning their standard therapy for their specific disease The primary objective of this study is to identify biomarkers of temsirolimus activity
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