Cancer Type: Malignant Hematology
Study Type: Treatment
NCT#: NCT04620681
Phase: Phase I/II
Principal Investigator: Elmariah, Hany
CD8 Depleted, Non-Engrafting, HLA Mismatched Unrelated Donor Lymphocyte Infusion in Patients with MDS and Secondary AML
The purpose of the study is to determine the safety of an investigational treatment for myelodysplastic syndrome (MDS) after the first therapy (such as azacitidine or decitabine) stops working or after progression of MDS to acute myeloid leukemia (AML).
1. Determine the maximum tolerated dose (MTD) of CD8-depleted non-engrafting human leukocyte antigen (HLA) mismatched unrelated donor lymphocyte infusion (NE-DLI) in patients with myeloid malignancies. 2. Estimate the response rate to therapy with CD8-depleted NE-DLI in patients with myelodysplastic syndrome (MDS) who have failed therapy with hypomethylating agents (HMAs) or untreated patients with acute myeloid leukemia (AML) secondary to an antecedent hematologic disease (sAML).
Chemotherapy (NOS); Therapy (NOS)
Cladribine (); Cytarabine (Cytosine Arabinoside); Daunomycin (daunorubicin); G-CSF (); Idarubicin (); Zevados (Idarubicin); daunorubicin ()
If you are interested in learning more about clinical trials, our clinical trial navigators can discuss your options and recommend opportunities that may be suitable for you. Call 813-745-6100 or 1-800-679-0775 (toll-free) or submit a clinical trials inquiry form.
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