PTK 787 and Gleevec in Patients With AML, AMM, and CML-BP

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

9

Participants

Timeline

Start Date

July 31, 2004

Primary Completion Date

October 31, 2006

Study Completion Date

October 31, 2006

Conditions
Acute Myelogenous LeukemiaAgnogenic Myeloid MetaplasiaChronic Myelogenous Leukemia
Interventions
DRUG

Imatinib Mesylate (Gleevec)

"600 mg by mouth every day (for AML, CML-BP) for a 28 day cycle.~400 mg by mouth every day (for AMM) for a 28 day cycle."

DRUG

PTK 787 (vatalanib)

"For 1 week prior to receipt of the study combination regimen, all patients will receive single agent PTK 787 at the dose specified for that dose level of the study combination regimen to allow stabilization of PTK 787 levels.~Starting dose: 250 mg by mouth every day for a 28 day cycle."

Trial Locations (1)

77030

M.D. Anderson Cancer Center, Houston

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Novartis

INDUSTRY

lead

M.D. Anderson Cancer Center

OTHER

NCT00088231 - PTK 787 and Gleevec in Patients With AML, AMM, and CML-BP | Biotech Hunter | Biotech Hunter