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Clinical Trial Summary

This is a single arm open label phase II clinical trial. Adult patients with hematological malignancies undergoing allogeneic HSCT from matched-related or unrelated donor are eligible for the study if they meet the standard criteria defined in the investigator's institutional standard operation procedures (SOPs), meet all inclusion criteria, and do not satisfy any exclusion criteria. Patients will receive reduced-intensity or myeloablative conditioning regimen of fludarabine, busulfan, and rabbit anti-thymocyte globulin (rATG). Patients will receive PTCyBor as GvHD prophylaxis.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03945591
Study type Interventional
Source NYU Langone Health
Contact
Status Completed
Phase Phase 2
Start date June 20, 2019
Completion date January 4, 2024

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