Haplo-identical SCT for High Risk (HR) Hematologic Malignancies w/Post-Transplant In-Vivo T-cell Depletion

Withdrawn before enrolling · Phase 1/Phase 2

Conditions studied: Leukemia, Lymphoma, MDS

In brief

Although a majority of children with leukemia and most hematological malignancies (Hodgkin's and Non-Hodgkin's lymphomas) can be cured with conventional chemotherapy, a subset of patients with resistant/recurrent high-risk disease are not cured with conventional treatment regimens. Investigators hypothesize that HSCT from a partially matched donor can be safe and effective for patients with very high risk hematologic malignancies when combined with post-transplant cyclophosphamide for prevention of graft-vs-host disease (GVHD).

Key facts

Study ID
NCT02053545
Run by
Ann & Robert H Lurie Children's Hospital of Chicago
People needed
0
Starts
2013-12-01
Expected to finish
2017-05-11
Last updated by the study team
2019-08-30

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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