Precision-T: A Randomized Study of Orca-T in Recipients Undergoing Allogeneic Transplantation for Hematologic Malignancies
a study on Acute Myeloid Leukemia Leukemia Myelodysplastic Syndrome Hematologic Malignancy Allogeneic Hematopoietic Cell Transplantation Hematopoietic Cell Transplantation Hematologic Neoplasms Lymphoma
Summary
- Eligibility
- for people ages 18-65 (full criteria)
- Location
- at Los Angeles, California and other locations
- Dates
- study startedcompletion around
Description
Summary
This study will evaluate the safety, tolerability, and efficacy of Orca-T, an allogeneic stem cell and T-cell immunotherapy biologic manufactured for each patient (transplant recipient) from the mobilized peripheral blood of a specific, unique donor. It is composed of purified hematopoietic stem and progenitor cells (HSPCs), purified regulatory T cells (Tregs), and conventional T cells (Tcons) in participants undergoing myeloablative allogeneic hematopoietic cell transplant transplantation for hematologic malignancies.
This posting represents the Phase III component of Precision-T. The Precision-T Ph1b component is described under NCT04013685.
Official Title
A Randomized Phase III Trial of Patients With Advanced Hematologic Malignancies Undergoing Allogeneic Hematopoietic Cell Transplantation With Either Orca-T, a T-cell-Depleted Graft With Additional Infusion of Conventional T Cells and Regulatory T Cells, or Standard-of-Care Allogeneic Graft
Details
Cross reference NCT04013685
Keywords
Acute Myeloid Leukemia, Acute Lymphoid Leukemia, Mixed Phenotype Acute Leukemia, Undifferentiated Leukemia, Myelodysplastic Syndrome, Acute Leukemia, Therapy-Related Myelodysplastic Syndrome, hematopoietic stem cell transplantation, Myelodysplastic syndromes, matched related donor, matched unrelated donor, Leukemia, Preleukemia, Hematologic Neoplasms, Lymphoid Leukemia, Precursor Cell Lymphoblastic Leukemia-Lymphoma, Syndrome, Acute Disease, Orca-T
Eligibility
You can join if…
Open to people ages 18-65
- Matched to a related or unrelated donor who is an 8/8 match for HLA-A, -B, -C, and DRB1
- Diagnosed with one of the following diseases:
- Acute myeloid, lymphoid or mixed phenotype leukemia in complete remission (CR) or CR with incomplete hematologic recovery (CRi), with or without the presence of known minimal residual disease
- Myelodysplastic syndromes (MDS) that are indicated for alloHSCT per 2017 International Expert Panel recommendations and/or have therapy-related/secondary MDS, with ≤ 10% blast burden in the bone marrow
- Planned to undergo MA-alloHCT including one of the following myeloablative conditioning regimens:
- TBI/Cy
- TBI/Etoposide
- BFT
- Cardiac ejection fraction at rest ≥ 45% or shortening fraction of ≥ 27% by echocardiogram or radionuclide scan (MUGA)
- Diffusing capacity of the lung for carbon monoxide (DLCO) (adjusted for hemoglobin) ≥ 50%
- Negative serum or urine beta-HCG test in females of childbearing potential
- ALT/AST < 3 times ULN
- Recipients in screening must screen negative for SARS-CoV-2 RNA using a PCR-based test
- Disease Risk Index (DRI) overall risk categorization of intermediate or high
- Total bilirubin ≤ upper limit of normal (ULN)
- Estimated glomerular filtration rate (eGFR) ≥ 60 mL/minute
You CAN'T join if...
- Prior allogeneic HCT
- Currently receiving corticosteroids or other immunosuppressive therapy. Topical corticosteroids or oral systemic corticosteroid doses less than or equal to 10 mg/day are allowed.
- Planned donor lymphocyte infusion (DLI)
- Planned pharmaceutical in vivo or ex vivo T cell depletion
- Recipient positive anti-donor HLA antibodies against a mismatched allele in the selected donor
- Karnofsky performance score < 70%
- Hematopoietic cell transplantation-specific Comorbidity Index (HCT-CI) > 4
- Uncontrolled bacterial, viral or fungal infections at time of enrollment
- Seropositive for HIV-1 or -2, HTLV-1 or -2, Hepatitis B sAg, Hepatitis C antibody
- Known allergy or hypersensitivity to, or intolerance of, tacrolimus
- Documented allergy or hypersensitivity to iron dextran or bovine, murine, algal or Streptomyces avidinii proteins
- Any uncontrolled autoimmune disease requiring active immunosuppressive treatment
- Concurrent malignancies or active disease within 1 year, except non-melanoma skin cancers that have been curatively resected
- Psychosocial circumstances that preclude the patient being able to go through transplant or participate responsibly in follow up care
- Women who are pregnant or breastfeeding
- Women of childbearing potential (WOCBP) or men who have sexual contact with WOCBP unwilling to use effective forms of birth control or abstinence for one year after transplantation
Locations
- Ronald Reagan UCLA Medical Center
Los Angeles California 90095 United States - City of Hope
Duarte California 91010 United States
Details
- Status
- in progress, not accepting new patients
- Start Date
- Completion Date
- (estimated)
- Sponsor
- Orca Biosystems, Inc.
- ID
- NCT05316701
- Phase
- Phase 3 research study
- Study Type
- Interventional
- Participants
- Expecting 174 study participants
- Last Updated