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Safety and Tolerability of HSC835 in Patients With Hematological Malignancies Summary This study evaluated the safety and tolerability of using HSC835 in patients with hematological malignancies.
View Eligibility Criteria Eligibility Criteria Inclusion Criteria: Patients with a diagnosis that qualifies them for a DUCBT Absence of recent active mold infection 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 Extensive prior chemotherapy Prior myeloablative allotransplantation or autologous transplant.
Check Your Eligibility
Let’s see if you might be eligible for this study.
What is your age and gender ?
There is 1 Location for this study
Novartis Investigative Site Minneapolis Minnesota, 55455, United States
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