Clinical Trial

Addition of Venetoclax to Combined Hematopoietic Stem Cell and Kidney Transplantation

Not Yet Recruiting Early Phase 1
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Summary
The primary objective is to assess the safety of the addition of venetoclax to reduced intensity conditioning for HLA-matched and haploidentical combined HSC and kidney transplantation as measured by stable full donor hematopoiesis and absence of CTCAE grade IV or V toxicity attributable to venetoclax.
Trial Details
NCT Number NCT07358195
Lead Sponsor Massachusetts General Hospital
Conditions Kidney Failure Chronic, Stem Cell Transplant, Stem Cell Transplant Complications, Tolerance, Hematologic Cancer
Enrollment 3 participants
Start Date 2026-07
Primary Completion 2028-12 (estimated)
Study Completion 2029-12 (estimated)
Updated on ClinicalTrials.gov 2026-01-22