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Clinical Trial Summary

The purpose of this phase 1 study is to determine the optimal dose of the immune suppressive drug, cyclophosphamide, following standard allogeneic stem cell transplant in patients aged >/= 70 years with hematologic malignancies.


Clinical Trial Description

The patients will receive a standard dose, or a reduced amount of the immune suppressive drug, cyclophosphamide, that is routinely administered after the transplant procedure. The following procedures will be performed: cardiac MRI scans and/or transthoracic echocardiogram (TTE); laboratory tests, geriatric assessments and tests to measure strength and stability. Participation in the study is expected to last up to one year with follow-up visits occurring on Day +30, Day +100, Day +180 and Day +365 following allogenic stem cell transplant. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05849207
Study type Interventional
Source Cedars-Sinai Medical Center
Contact Amy Oppenheim
Phone 310-423-3713
Email Amy.Oppenheim@cshs.org
Status Recruiting
Phase Phase 1
Start date October 24, 2023
Completion date July 1, 2028

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