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Anti-tumor antibiotic
Allogeneic Hematopoietic Stem Cell Transplantation for Acute Myeloid Leukemia
Phase 2
Waitlist Available
Led By Filippo Milano
Research Sponsored by Fred Hutchinson Cancer Research Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up from the time of randomization up to 2 years post-randomization. for descriptive purposes, we shall also report survival and relapse-free survival from time of transplant up to 2 years post-transplant among patients who receive a transplant.
Awards & highlights
No Placebo-Only Group
Summary
This trial studies whether giving a specific type of chemotherapy before a stem cell procedure is more effective than doing the procedure immediately for patients with certain severe blood cancers. The chemotherapy aims to reduce cancer cells and prepare the body for new healthy cells. This newer treatment has shown promising results in improving intensive chemotherapy for a type of blood cancer.
Eligible Conditions
- Acute Myeloid Leukemia
- Myeloid Neoplasm
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ from the time of randomization up to 2 years post-randomization. for descriptive purposes, we shall also report survival and relapse-free survival from time of transplant up to 2 years post-transplant among patients who receive a transplant.
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~from the time of randomization up to 2 years post-randomization. for descriptive purposes, we shall also report survival and relapse-free survival from time of transplant up to 2 years post-transplant among patients who receive a transplant.
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Overall Survival
Secondary study objectives
Frequencies of the Types of Transplantation Received
Rate of Transplantation
Relapse-free Survival
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Arm B (CPX-351, alloHCT)Experimental Treatment2 Interventions
Patients receive CPX-351 IV over 90 minutes on days 1, 3, and 5. Treatment may repeat for an additional cycle for a total of 2 cycles (on days 1 and 3 only of cycle 2) in the absence of disease progression or unacceptable toxicity. Within 60 days after completion of CPX-351, patients undergo alloHCT.
Group II: Arm A (alloHCT)Active Control1 Intervention
Patients undergo alloHCT.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Allogeneic Hematopoietic Stem Cell Transplantation
2012
Completed Phase 2
~1240
Liposome-encapsulated Daunorubicin-Cytarabine
2016
Completed Phase 2
~100
Find a Location
Who is running the clinical trial?
Fred Hutchinson Cancer Research CenterLead Sponsor
443 Previous Clinical Trials
147,993 Total Patients Enrolled
Fred Hutchinson Cancer CenterLead Sponsor
569 Previous Clinical Trials
1,342,128 Total Patients Enrolled
Jazz PharmaceuticalsIndustry Sponsor
249 Previous Clinical Trials
34,840 Total Patients Enrolled
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