Stopped: PI has left IU with no plan to initiate study at IU
This is an open label Phase I-II study to determine the safe doses of bortezomib, sitagliptin, and PTCy (Phase I) with expansion into a phase II trial to determine efficacy in improving survival.
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Maximum tolerated dose
Timeframe: in the first 30 days post-transplant
proportion of patients developing grades 3-4 non-hematological toxicity defining DLT assessed by CTCAE version 5.0
Timeframe: in the first 30 days post-transplant
Proportion of patients alive and free of grade II-IV acute GVHD (graft-versus-host disease)
Timeframe: Baseline to day +100
Cumulative incidence of grade II-IV acute GVHD
Timeframe: through study completion (i.e. up to 5 years)