Phase II Trial of Decitabine in Patients With Chronic Myelogenous Leukemia Chronic Phase Who Are Refractory to Imatinib Mesylate (Gleevec)
- Conditions
- Chronic Myelogenous Leukemia
- Registration Number
- NCT00042016
- Lead Sponsor
- Astex Pharmaceuticals, Inc.
- Brief Summary
To determine the safety and efficacy of decitabine in patients with Philadelphia chromosome-positive chronic myelogenous leukemia chronic phase that were previously treated with imatinib mesylate (STI 571) and became resistant/refractory or were found to be intolerant to the drug.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 40
Not provided
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (8)
Scripps Clinic
πΊπΈEscondido, California, United States
Metro-Minnesota CCOP
πΊπΈSt. Louis Park, Minnesota, United States
City of Hope Medical Center
πΊπΈDuarte, California, United States
USC/Norris Cancer Center
πΊπΈLos Angeles, California, United States
New York Medical College
πΊπΈValhalla, New York, United States
University of Texas MD Anderson Cancer Center
πΊπΈHouston, Texas, United States
Princess Margaret Hospital
π¨π¦Toronto, Ontario, Canada
Liberty Hematology/Oncology
πΊπΈColumbia, South Carolina, United States