RecruitingPhase 2

Trial of Orca-T Following Reduced Intensity or Nonmyeloablative Conditioning in Patients With Acute Myeloid Leukemia or Myelodysplastic Syndrome

A Phase 2 Trial of Orca-T Following Reduced Intensity or Nonmyeloablative Conditioning in Patients With Acute Myeloid Leukemia or Myelodysplastic Syndrome

Who can join

As published by the study on ClinicalTrials.gov. "Not stated" means the study hasn't said — ask the study team.

Age
18 Years and older
Sex
All sexes
Healthy volunteers
Not accepted
Compensation
Not stated

Other requirements are listed under Eligibility below. Only the study team can confirm whether you can join.

What to expect

No one can promise a trial will help you personally — that is what the research is trying to find out.

What participation involves

Not stated in the study description — ask the study team about visits and procedures.

Compensation
Not stated
  • Study-related exams and procedures are typically provided at no cost. This is how many trials work in general — confirm the details for this study with the study team.
  • Participants are monitored closely by the research team throughout the study.
  • Some participants may receive access to an investigational treatment, which is still being studied.
  • Your participation helps researchers learn whether this approach could help future patients.

About this study

In plain language

This study tests how safe Orca-T is and how well it works for adults with certain types of leukemia or myelodysplastic syndrome, a bone marrow disease. Orca-T uses stem cells and immune cells from a donor. It is for people having a donor stem cell transplant with a less intense treatment plan before the transplant.

This study will evaluate the safety, tolerability, and efficacy of Orca-T in participants undergoing reduced intensity or non-myeloablative allogeneic hematopoietic cell transplantation (alloHCT) for hematologic malignancies. Orca-T is 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).

Compensation is read from the study's own description and may be missing — always confirm with the study team.

Eligibility

Who can join

  • Be age 18 or older.
  • Have acute myeloid or mixed phenotype leukemia in remission (signs of cancer have gone away), even if blood counts have not fully recovered or small amounts of cancer remain.
  • Or have myelodysplastic syndrome that meets the study’s transplant rules, with no more than 10% immature cells called blasts in the bone marrow.
  • Plan to receive one of the study’s less intense treatments before transplant: radiation, thiotepa, and fludarabine; or fludarabine, cyclophosphamide, and radiation.
  • Have a related or unrelated donor who matches all 8 required immune-system markers.
  • Meet kidney, heart, and lung test limits: kidney filtering rate at least 30; heart pumping fraction at least 40% or shortening fraction at least 22%; and lung gas-transfer score at least 40%.
  • Have liver enzymes below 5 times the upper normal limit and bilirubin below 3 times that limit. If able to become pregnant, have a negative pregnancy test.
  • Be judged by the study doctor as unable to receive a full-intensity donor stem cell transplant.

Who can't join

  • Have had a donor stem cell transplant before; plan to receive extra donor immune cells; or plan to have T cells removed or reduced with drugs.
  • Take drugs that weaken the immune system, or have uncontrolled autoimmune disease needing these drugs. Steroid skin treatments and oral steroid doses of 10 mg a day or less are allowed.
  • Have antibodies against a mismatched donor immune marker; a daily-activity score below 60%; or, for the reduced-intensity group only, a transplant health-problem score of 6 or higher.
  • Have an uncontrolled infection, or test positive for HIV, HTLV, hepatitis B surface antigen, or hepatitis C antibodies. Previously cured hepatitis C is allowed if the HCV NAT test finds no virus.
  • Cannot tolerate tacrolimus, or have an allergy to it, iron dextran, or proteins from cows, mice, algae, or Streptomyces avidinii bacteria.
  • Have had another cancer within 1 year, except nonmelanoma skin cancer removed by surgery with the aim of curing it.
  • Be pregnant or breastfeeding, or be unwilling to use effective birth control or avoid sex for 1 year after transplant if you or your sexual partner could become pregnant.
  • Have personal or social circumstances that prevent transplant or follow-up care, or a serious health problem or abnormal test result that could make participation unsafe or affect study results.

Simplified for readability. The official criteria below are what the study team uses.

Official eligibility criteria

Inclusion Criteria: 1. Age ≥18 years at the time of enrollment 2. Diagnosed with 1 of the following diseases: 1. Acute myeloid, 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. 2. Myelodysplastic syndrome that is indicated for alloHCT per the 2017 International Expert Panel recommendations and/or therapy-related/secondary MDS as defined by the World Health Organization (WHO) classification of myeloid malignancies, with ≤10% blast burden in the bone marrow. 3. Planned to undergo 1 of the following preparative regimens as per Investigator discretion: 1. RIC cohort: Planned RIC-alloHCT including RIC regimen with TBI/thiotepa/fludarabine 2. NMA cohort: Planned NMA-alloHCT including NMA regimen with fludarabine/cyclophosphamide/TBI 4. Identified related or unrelated donor who is an 8/8 match for HLA-A, -B, -C, and -DRB1 5. Estimated glomerular filtration rate ≥30 mL/minute 6. Cardiac ejection fraction at rest ≥40% or shortening fraction of ≥22% by echocardiogram or radionuclide scan (MUGA) 7. Diffusing capacity of the lung for carbon monoxide (adjusted for hemoglobin) ≥40% 8. Negative serum or urine β-HCG test in persons of childbearing potential 9. Alanine transaminase (ALT)/aspartate transaminase (AST) \<5 times the upper limit of normal (ULN) 10. Total bilirubin \<3 × ULN 11. Deemed ineligible for a fully myeloablative alloHCT per assessment of the principal investigator Exclusion Criteria: 1. Prior alloHCT 2. Currently receiving corticosteroids or other immunosuppressive therapy. Topical corticosteroids or oral systemic corticosteroid doses less than or equal to 10 mg/day are allowed. 3. Planned donor lymphocyte infusion (DLI) 4. Planned pharmaceutical in vivo or ex vivo T-cell depletion 5. Recipient-positive antidonor HLA antibodies against a mismatched allele in the selected donor 6. Karnofsky performance score \<60% 7. For RIC cohort only: HCT-Specific Comorbidity Index (HCT-CI) ≥6 8. Uncontrolled bacterial, viral, or fungal infection (currently taking antimicrobial therapy and with progression or no clinical improvement) at the time of enrollment 9. Seropositive for HIV-1 or -2, HTLV-1 or -2, hepatitis B surface antigen, or HCV antibody unless previously treated with curative therapy and are HCV NAT negative 10. Known allergy or hypersensitivity to or intolerance of tacrolimus 11. Documented allergy or hypersensitivity to iron dextran or bovine, murine, algal, or Streptomyces avidinii proteins 12. Any uncontrolled autoimmune disease requiring active immunosuppressive treatment 13. Concurrent malignancy within 1 year except nonmelanoma skin cancer that has been curatively resected 14. Psychosocial circumstances that preclude the participant being able to go through transplantation or participate responsibly in follow-up care 15. Persons who are pregnant or breastfeeding 16. Person of childbearing potential (POCBP) or men who have sexual contact with POCBP who are unwilling to use effective forms of birth control or abstinence for 1 year after transplantation. 17. Any serious medical condition or abnormality in clinical laboratory tests that, in the investigator's or medical monitor's judgment, precludes the recipient's safe participation in and completion of the trial or which could affect compliance with the protocol or interpretation of results

Study sites (6)

CA

FL

NJ

NY

OR

TN