Active, not recruiting
Phase 1/2
A First-in-Human Study of HLA-Partially to Fully Matched Allogenic Cryopreserved Deceased Donor Bone Marrow Transplantation for Patients With Hematologic Malignancies
Condition(s) studied
Acute LeukemiaAcute Lymphoblastic LeukemiaAcute Myeloid LeukemiaAcute Biphenotypic LeukemiaAcute Undifferentiated LeukemiaCLL (Chronic Lymphocytic Leukemia)Chronic Myeloid Leukemia (CML)MDS (Myelodysplastic Syndrome)Non-Hodgkin LymphomasHodgkins LymphomaCutaneous T Cell Lymphomas (CTCL)
Investigational drug(s) / intervention(s)
Ossium HPC Marrow, Bone Marrow TransplantPre-transplant conditioning - Myeloablative (MAC)Pre-transplant conditioning - Reduced Intensity (RIC)Post-transplant treatment
Ossium HPC Marrow, Bone Marrow Transplant: Hematopoetic Cell Transplantation
Pre-transplant conditioning - Myeloablative (MAC): Regimen A or Regimen B
Pre-transplant conditioning - Reduced Intensity (RIC): Regimen C or Regimen D
Post-transplant treatment: Post-transplant treatment
Study summary
The goal of this clinical trial is to determine the safety and feasibility of allogeneic transplantation with bone marrow from a deceased donor in patients with acute and chronic leukemias, myelodysplastic syndrome, and certain lymphomas. Patients will either receive myeloablative conditioning or reduced intensity conditioning regimen prior to the transplant. Patients will be followed for 56 days for safety endpoints and remain in follow-up for one year.
Eligibility
Inclusion Criteria:
* Patient has the ability to provide informed consent according to the applicable regulatory and local institutional requirements
* Male or female, aged ≥18 and ≤65 years for patients receiving MAC (Regimen A or Regimen B); aged ≥18 and ≤75 years for patients receiving RIC (Regimen C or D)
* Patient must require allogeneic HCT per the discretion of the treating physician
* Patient must be high-resolution, HLA partially or fully matched (4-8/8 allele matched at HLA-A, -B, -C, DRB1) to an available Ossium HPC, Marrow product
* Stated willingness to comply with all study procedures and availability for the duration of the study
* Diagnosed with malignant hematologic disease including:
1. Acute leukemia \[acute lymphoblastic leukemia (ALL), acute myeloid leukemia (AML), acute biophenotypic leukemia (ABL), or acute undifferentiated leukemia (AUL)\], MDS without fibrosis, or chronic leukemia (CLL, CML) in the first remission or beyond with ≤5% marrow blasts documented by bone marrow assessment and no circulating blasts or extra-medullary disease within 42 days prior to anticipated start of conditioning
2. Chemosensitive non-Hodgkin's lymphomas, Hodgkin's lymphoma, or cutaneous T cell lymphomas in the first remission or beyond documented by PET/CT imaging and bone marrow assessment within 42 days prior to anticipated start of conditioning
* Karnofsky performance status score ≥70% (MAC) or ≥60% (RIC)
* HCT comorbidity index (HCT-CI) ≤5
* Adequate organ function defined as:
1. Cardiac: LVEF at rest ≥40% (RIC) or LVEF at rest ≥45% (MAC)
2. Pulmonary: DLCO, FEV1, FVC ≥50% predicted by pulmonary function tests (PFTs). DLCO value may be corrected for hemoglobin.
3. Hepatic: total bilirubin ≤2.0 mg/dL, and ALT, AST, and ALP \<3 x upper limit normal (ULN), unless ALT, AST, and/or ALP are disease related
4. Renal: SCr within 1.5x normal range for age. If SCr is outside normal range for age, CrCl\> 60 mL/min/1.73m2 must be obtained (measured by 24-hour urine specimen or nuclear glomerular filtration rate (GFR), or calculated GFR)
Exclusion Criteria:
* Availability of suitable graft from living donor (defined as 7/8 or 8/8 HLA-matched related or unrelated donors, haploidentical donors, or cord blood donors)
* Prior autologous or allogeneic HCT
* Pregnancy or lactation
* Ongoing treatment with an investigational drug used for disease-related treatment within 5 half-lives of the drug
* Current uncontrolled bacterial, viral or fungal infection defined as currently taking medication with evidence of progression of clinical symptoms or radiologic findings
* Any condition(s) or diagnosis, both physical or psychological, or physical exam finding that in the investigator's opinion precludes participation
Primary outcome measure(s)
- Neutrophil Engraftment — Day 28
Neutrophil engraftment is defined as achieving an absolute neutrophil count (ANC) of greater than or equal to 500/µL for 3 consecutive measurements on 3 different days by Day 28.
- Serious Adverse Events — Day 56
Occurrence of any event classified as SAE. The time of occurrence of each serious adverse event will be recorded.
- CTCAE Grade 3/4 Adverse Events (AEs) — Day 56
Occurrence of any event classified as grade 3/4 AE attributed to Ossium HPC, Marrow per the CTCAE v5.0 guidelines. The time of the occurrence of each event will be recorded.
- CTCAE Grade 3/4 Adverse Events (AEs) attributed to infusion of Ossium HPC, Marrow — Day 28
Occurrence of any event classified as grade 3 or higher attributed to Ossium HPC, Marrow infusion per the CTCAE v5.0 guidelines. The time of the occurrence will be recorded.
- Death — Day 56
The time of death will be recorded for each expired patient.
Trial sites (9)
| Facility | City | Region | Status |
| City of Hope |
Duarte |
California |
|
| Moffitt Cancer Center |
Tampa |
Florida |
|
| Emory University - Winship Cancer Institute |
Atlanta |
Georgia |
|
| Henry Ford Cancer Institute |
Detroit |
Michigan |
|
| Oregon Health and Science University |
Portland |
Oregon |
|
| TriStar Bone Marrow Transplant |
Nashville |
Tennessee |
|
| St. David's South Austin Medical Center |
Austin |
Texas |
|
| Methodist Hospital, Texas Transplant |
San Antonio |
Texas |
|
| University of Utah - Huntsman Cancer Institute |
Salt Lake City |
Utah |
|
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