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.
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
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)