Gleevec Trial in Patients With Newly Diagnosed Chronic Phase Chronic Myelogenous Leukemia
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|ClinicalTrials.gov Identifier: NCT00081926|
Recruitment Status : Completed
First Posted : April 29, 2004
Last Update Posted : November 23, 2009
This study will evaluate the molecular response to high dose Gleevec in newly diagnosed patients with Chronic Myelogenous Leukemia (CML) in Chronic Phase. This study will evaluate the ability of Gleevec to reduce the amount of abnormal protein that occurs in patients with CML.
Patients who are eligible to participate will be treated for 18 months. This trial will include male or female patients 18 years or older who are newly diagnosed (within 6 months) with CML.
|Condition or disease||Intervention/treatment||Phase|
|Chronic Myelogenous Leukemia||Drug: Gleevec||Phase 4|
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||112 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Study Start Date :||October 2003|
|Estimated Study Completion Date :||March 2007|
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00081926
|United States, New Jersey|
|Novartis RIGHT Trial Hotline|
|East Hanover, New Jersey, United States|