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Search / Trial NCT00386373

Use and Tolerability of Imatinib Mesylate (Gleevec) in Leukemia Patients

Launched by M.D. ANDERSON CANCER CENTER · Oct 10, 2006

Trial Information

Current as of June 23, 2025

Completed

Keywords

Chronic Myeloid Leukemia Cml All Aml Leukemia Imatinib Mesylate Gleevec Philadelphia Positive Bone Marrow Transplant Bmt Stem Cell Transplant Sct

ClinConnect Summary

Imatinib mesylate is an FDA-approved, commercially available drug for patients with acute or chronic leukemias carrying the Philadelphia chromosome. Women who are able to have children must have a negative blood pregnancy test before taking this drug

No earlier than three weeks after the bone marrow or stem cell transplant, you will start taking imatinib mesylate by mouth. You will take it once or twice a day until roughly 100 days following the transplant or until you are released from the Houston area by your M. D. Anderson physician. Imatinib mesylate should be taken with a meal and a g...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • 1. Patients with Ph(+) CML and/or CML with bcr-abl rearrangement and diploid cytogenetics not eligible for protocols of higher priority (e.g. ID02-901, DM99-081, DM97-206, etc).
  • 2. The disease must be beyond first chronic phase according to IBMTR criteria (i.e. accelerated phase, blastic phase, second chronic phase) at the time of transplant.
  • 3. Patients with Ph(+) acute lymphocytic (or myeloid) leukemia.
  • 4. Patients with diploid cytogenetics but molecular evidence of bcr-abl rearrangement are also eligible.
  • 5. Age \>/= 16 years
  • 6. Unsupported ANC at least 1500 and unsupported platelet count of at least 50K following BMT.
  • 7. Patients may have received prior chemotherapy for their disease or be previously untreated.
  • 8. Patients must have received an allogeneic bone marrow or stem cell transplant. Allogeneic transplant types may include matched sibling donors, mismatched related donors, or unrelated donors. All preparative regimens acceptable.
  • 9. Signed informed consent
  • 10. Zubrod status \</= 3
  • 11. Adequate hepatic (bilirubin \</= 3 mg/dl, transaminases \< 4 x upper limit of normal) and renal function (serum creatinine \</= 3 mg/dl )
  • Exclusion Criteria:
  • 1. Grade III/IV cardiac problems as defined by the NYHAC
  • 2. History of hypersensitivity to imatinib
  • 3. Pregnant and lactating women
  • 4. HIV positive

About M.D. Anderson Cancer Center

The University of Texas MD Anderson Cancer Center is a leading institution dedicated to cancer care, research, education, and prevention. As one of the world’s most respected cancer centers, MD Anderson focuses on innovative treatment approaches and groundbreaking clinical trials aimed at improving patient outcomes. With a multidisciplinary team of experts and state-of-the-art facilities, the center is committed to advancing cancer research and providing comprehensive, personalized care to patients. MD Anderson's clinical trials play a pivotal role in translating scientific discoveries into effective therapies, positioning the center at the forefront of cancer treatment and research.

Locations

Houston, Texas, United States

Patients applied

0 patients applied

Trial Officials

Paolo Anderlini, MD

Principal Investigator

M.D. Anderson Cancer Center

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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