Expired Study
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Madison, Wisconsin 53972


Purpose:

This study will assess the feasibility of utilizing a reduced intensity conditioning regimen, in the setting of haploidentical transplantation, for patients with recurrent acute lymphoblastic leukemia (ALL), AML and high risk or refractory solid tumors. In addition, the feasibility and safety of administering post-transplant NK cell infusions will be evaluated. Data obtained from this study will help determine the efficacy of allogeneic HSCT in the treatment of pediatric sarcomas and add to the small body of literature utilizing haploidentical HSCT to treat acute leukemia in pediatric patients. This study will also further elucidate the role of NK cells in mediating a graft vs. tumor effect in allogeneic HSCT. The main benefit to society is that this study will explore a novel therapy for children with highly refractory cancer who are felt to be incurable with conventional approaches. If feasibility is demonstrated, and there is evidence of anti-tumor activity, then this will open up a new area of clinical research to better define the efficacy of this approach for specific childhood malignancies.


Criteria:

Inclusion Criteria: - Solid tumors that have failed auto transplant or are ineligible to receive auto transplant - Relapsed AML in 1st relapse or 2nd or 3rd CR - Relapsed ALL if they fail to attain an initial remission or if they relapse within 1 year following the discontinuation of chemotherapy. - Greater than or equal to 6 months and <26 years old - Suitable haploidentical donor available Exclusion Criteria: - Leukemia with >25% blasts in bone marrow at the time of admission to the HSCT unit. - Serum bilirubin >3 mg/dl - GFR <40 ml/min/1.73 mw - Cardiac left ventricular ejection fraction <40% - HIV+ - Pregnant


NCT ID:

NCT00582816


Primary Contact:

Principal Investigator
Kenneth DeSantes, M.D.
University of Wisconsin, Madison


Backup Contact:

N/A


Location Contact:

Madison, Wisconsin 53972
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: January 18, 2018

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