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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

What this study is about

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.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Ossium HPC Marrow, Bone Marrow Transplant
  • 2.Post-transplant treatment
  • 3.Pre-transplant conditioning - Myeloablative (MAC)
  • +1 more

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Standard

How treatment is administered

Treatment Assignment
All receive treatment

Everyone gets the investigational treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

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