RecruitingPhase 2ACTRN12605000071628

Pilot cml autograft/glivec (STI571)/Intron A trial

Pilot study to determine the efficacy and safety of Glivec (STI571) alone and Glivec (STI571) plus Intron A in the early recovery phase post autologous blood or marrow transplant for advanced phase chronic myeloid leukaemia and Ph-positive acute lymphoblastic leukemia


Sponsor

Australasian Leukaemia and Lymphoma Group

Enrollment

48 participants

Start Date

Jan 7, 2002

Study Type

Interventional

Conditions


Eligibility

Sex: Both males and femalesMin Age: 18 YearssMax Age: 70 Yearss

Plain Language Summary

Simplified for easier understanding

This study looks at a combination treatment for a type of blood cancer called CML (chronic myeloid leukaemia) or a related condition called ALL (acute lymphoblastic leukaemia) that involves a specific chromosome abnormality. The treatment combines a stem cell transplant using the patient's own stem cells (autologous transplant) with two medicines: Glivec (imatinib) and Intron A (interferon). Researchers want to see how safe and effective this combination is. You may be eligible if: - You are between 18 and 70 years old - You have been diagnosed with Ph chromosome-positive CML that is not in first chronic phase, or Ph-positive ALL, or CML that has become resistant to Glivec - You have stored (frozen) stem cells available from a previous collection - Your liver, kidney, and bone marrow function are within acceptable levels - You have given written informed consent You may NOT be eligible if: - There are no specific exclusion criteria listed beyond meeting all inclusion requirements and standard safety measures Talk to your doctor about whether this trial might be right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

This study evaluates the addition of Glivec (Imatinib) at variable time points in the first weeks to months post autologous stem cell transplant to evaluate safety and efficacy in the treatment of Phi

This study evaluates the addition of Glivec (Imatinib) at variable time points in the first weeks to months post autologous stem cell transplant to evaluate safety and efficacy in the treatment of Philadelphia chromosome positive leukemia.


Locations(1)

Australia

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ACTRN12605000071628