Overview
Phase 2 Haplotype Mismatched HSCT in Patients With Hematological Malignancies
Status:
Terminated
Terminated
Trial end date:
2017-07-28
2017-07-28
Target enrollment:
0
0
Participant gender:
All
All
Summary
The purpose of this study is to determine if haplotype-mismatched HSCT is associated with an improvement in treatment-related mortality (TRM) rate at 6 months.Phase:
Phase 2Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Sherif S. FaragTreatments:
Antilymphocyte Serum
Fludarabine
Fludarabine phosphate
Thiotepa
Thymoglobulin
Criteria
Inclusion Criteria:- Patients must have histologically documented AML, ALL, MDS, CML, Acute myeloid
leukemia (AML) with one or more of the following criteria
- CR 1 with poor risk features
- CR 2, or higher order CR
- Acute lymphoblastic leukemia (ALL) with one of the following criteria
- CR 1 with poor risk features
- CR 2, or higher order CR
- Myelodysplasia, RAEB I
- Donor has been identified
- Age ≤ 65 years.
- Performance Status 0-1.
Exclusion Criteria:
- Patients relapsing <6 months after autologous SCT are not eligible.
- Patients with active infections requiring oral or intravenous antibiotics are not
eligible for enrollment until resolution of infection.
- Non-pregnant and non-nursing