Viewing Study NCT00171899



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Last Modification Date: 2024-10-26 @ 9:16 AM
Study NCT ID: NCT00171899
Status: COMPLETED
Last Update Posted: 2017-02-23
First Post: 2005-09-13

Brief Title: Study Comparing Standard Dose and High-dose Imatinib Mesylate in Patients With Chronic Phase Philadelphia Chromosome Positive Ph Chronic Myelogenous Leukemia CML
Sponsor: Novartis Pharmaceuticals
Organization: Novartis

Study Overview

Official Title: Study Comparing Standard Dose and High-dose Imatinib Mesylate in Patients With Chronic Phase Ph CML
Status: COMPLETED
Status Verified Date: 2017-02
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 assess the role of high-dose imatinib mesylate in patients who have taken imatinib mesylate for at least 1 year at the standard dose in achieving a major molecular response a measure of the level of chronic myelogenous leukemia versus the standard dose
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