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Study details
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A First-in-Human Study of HLA-Partially to Fully Matched Allogeneic Cryopreserved Deceased Donor Bone Marrow Transplantation for Patients With Hematologic Malignancies

Ossium Health, Inc.
NCT IDNCT05589896ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1/2

Target enrollment

12

Study length

about 2.4 years

Ages

18–75

Locations

9 sites in CA, FL, GA +5

About this study

This trial is testing the safety and feasibility of a bone marrow transplant from a deceased donor in people with leukemia, myelodysplastic syndrome, and certain lymphomas. Participants will receive either myeloablative or reduced intensity conditioning before the transplant. They will be followed for 56 days to monitor safety and remain under follow-up for one year.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Ossium HPC Marrow, Bone Marrow Transplant
  • 2.Post-transplant treatment
  • 3.Pre-transplant conditioning - Myeloablative (MAC)
  • +1 more
PhasePhase 1/Phase 2
Primary goalCTCAE Grade 3/4 Adverse Events (AEs)

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low8%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

Endpoints

Primary: CTCAE Grade 3/4 Adverse Events (AEs), CTCAE Grade 3/4 Adverse Events (AEs) attributed to infusion of Ossium HPC, Marrow, Death, Serious Adverse Events

Body systems

Oncology