Reduced MBF Regimen for Patients >=55 Years With Myeloid Malignancies
Recruiting
Phase 2Interventional Study
Disease-free Survival
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Prior Safety Data
This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
55 – 65
Sex
Any
Trial phase
Phase 2
Study type
Interventional
Purpose
Treatment
Participants needed
61 (estimated)
Sponsor
Shanghai Jiao Tong University School of Medicine · Other
Who this trial is looking for
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In this multiple-center phase II study, the aim is to evaluate the clinical outcome of reduced intensity conditioning regimen with fludarabine (150mg/m2), busulfan (6.4mg/kg) and melphalan (100mg/m2) in patients with myeloid malignancies including AML, MDS and CMML \>=55 years.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Age 55-65
* patients with HLA-matched sibling donors, 9-10/10 matched unrelated donors or haplo-identical donors.
* patients with AML in remission, or MDS in any stage, or CMML in any stage
* inform consent provided
Exclusion Criteria:
* patients with abnormal liver (\>3N), …
Inclusion Criteria:
* Age 55-65
* patients with HLA-matched sibling donors, 9-10/10 matched unrelated donors or haplo-identical donors.
* patients with AML in remission, or MDS in any stage, or CMML in any stage
* inform consent provided
Exclusion Criteria:
* patients with abnormal liver (\>3N), renal (1.5N) or cardiac function
* patients with active infection
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