Viewing Study NCT01271166


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Study NCT ID: NCT01271166
Status: TERMINATED
Last Update Posted: 2011-01-06
First Post: 2011-01-04
Is Gene Therapy: True
Has Adverse Events: False

Brief Title: Glivec® Plus m-FOLFOX Avastin® in Advanced Colorectal Cancer
Sponsor: Novartis Pharmaceuticals
Organization:

Study Overview

Official Title: None
Status: TERMINATED
Status Verified Date: 2011-01
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 a Phase I, dose finding, multicentre study evaluating the maximal tolerated dose of Glivec® in combination with mFOLFOX-Avastin®. Patients will be enrolled into each dose level in 3 patient cohorts. Additional cohorts will be enrolled, or dose levels opened, subject to the toxicities observed. Once the MTD has been determined the dose level below will be re-opened and extra patients, to a total of 15, will be enrolled.
Detailed Description: None

Study Oversight

Has Oversight DMC:
Is a FDA Regulated Drug?:
Is a FDA Regulated Device?:
Is an Unapproved Device?:
Is a PPSD?:
Is a US Export?:
Is an FDA AA801 Violation?: