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A Phase I Trial of Host Dendritic Cell Infusion After Allogeneic Stem Cell Transplant for Prevention or for Treatment of Relapsed Disease in Patients With Advanced Hematologic Malignancies
The purpose of this study is to assess preliminary efficacy and to determine the safety and feasibility of ex vivo generated dendritic cell (HDC) infusion with and without donor lymphocyte infusion (DLI) after allogeneic stem cell transplant (SCT). We also wish to establish the feasibility of apheresis shipment as well as vaccine shipment and stability in the population.
Age
18 - 70 years
Sex
ALL
Healthy Volunteers
No
Mount Sinai Medical Center
New York, New York, United States
Start Date
August 1, 2009
Primary Completion Date
July 1, 2013
Last Updated
October 29, 2010
25
ESTIMATED participants
MSSM/BIIR HDC Vax-001 (Host Dendritic Cells)
BIOLOGICAL
Lead Sponsor
Icahn School of Medicine at Mount Sinai
NCT06179888
NCT06152575
Data Source & Attribution
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Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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View ClinicalTrials.gov Terms and ConditionsNCT04973605