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Safety and Tolerability of HSC835 in Patients With Hematological Malignancies Undergoing Single Umbilical Cord Blood Transplant Summary This study was designed to evaluate the safety and tolerability of HSC835 for clinical use as measured by the absence of graft failure at day 42 in excess of that currently observed with double umbilical cord blood (UCB) transplantation (DUCBT) with non-myeloablative (NMA) conditioning.
View Eligibility Criteria Eligibility Criteria Inclusion Criteria: Patients with a diagnosis that qualifies them for UCBT Adequate organ function Availability of eligible donor material Exclusion Criteria: Pregnancy or breastfeeding women and women of child-bearing potential unless two acceptable forms of contraception are being used Human immunodeficiency virus (HIV) infection Active infection
Check Your Eligibility
Let’s see if you might be eligible for this study.
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There is 1 Location for this study
Novartis Investigative Site Minneapolis Minnesota, 55455, United States
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