Recruiting
Phase 1

Orca-Q

Sponsor:

Orca Biosystems, Inc.

Code:

NCT03802695

Conditions

Acute Myeloid Leukemia

Myelodysplastic Syndromes

Mixed Phenotype Acute Leukemia

Acute Lymphoblastic Leukemia

Eligibility Criteria

Sex: All

Age: 12 - 70+

Healthy Volunteers: Not accepted

Interventions

OrcaGraft (Orca-Q)

Study Details

Brief summary:

This study will evaluate the safety, tolerability, and efficacy of engineered donor grafts ("OrcaGraft"/"Orca-Q") in participants undergoing allogeneic hematopoietic cell transplant (alloHCT) transplantation for hematologic malignancies.

Conditions

Acute Myeloid Leukemia

Myelodysplastic Syndromes

Mixed Phenotype Acute Leukemia

Acute Lymphoblastic Leukemia

Study ID

NCT03802695

Start date

Apr 8, 2019

Status verified date

Jun, 2026

Completion date

Dec, 2027

Anticipated

Primary completion date

Dec, 2027

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 12 - 70+

Healthy Volunteers: Not accepted

Key Inclusion Criteria:

1. Age at the time of enrollment:

1. For MAC with fully matched donor (Arm A with 8/8 donor and Arm C) and NMA/RIC: Age ≥ 12 and ≤ 78 years
2. For MAC with mismatched donors (Arm A with 7/8 donor and Arm B): Age ≥ 12 and ≤ 65 years
2. Diagnosed acute myeloid, lymphoblastic or mixed phenotype leukemia, or high or very high risk myelodysplastic syndrome (MDS) either in complete remission (CR) or with ≤ 10 percent of blast cells in bone marrow (BM)
3. Indicated for allogeneic hematopoietic stem cell transplant (alloHCT)
4. Matched to a 8/8 or 7/8 related or unrelated donor, or to a related haploidentical donor
5. Estimated glomerular filtration rate (eGFR) > 50 mL/minute (MAC with tacrolimus) or > 30 mL/minute (NMA/RIC or MAC without tacrolimus)
6. Cardiac parameters: Cardiac ejection fraction ≥ 45 percent (MAC) or ≥ 40 percent (NMA/RIC)
7. Diffusing capacity of the lung for carbon monoxide (DLCO) (adjusted for hemoglobin) ≥ 50 percent for MAC or ≥ 40 percent for NMA/RIC
8. Liver function: Total bilirubin < 1.5 times upper limit of normal (ULN) (MAC) or < 3 times ULN (NMA/RIC); alanine transaminase (ALT)/aspartate transaminase (AST) < 3 times ULN (MAC) or < 5 times ULN (NMA/RIC)
9. Participants enrolling on NMA/RIC-alloHCT arms must be deemed unfit for a myeloablative alloHCT per assessment of the principal investigator (PI)

Key Exclusion Criteria:

1. Prior alloHCT
2. Currently receiving corticosteroids or other immunosuppressive therapy except for approved disease-specific therapy for the patient's underlying hematologic malignancy. 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, e.g., post-transplant cyclophosphamide (Cy) or alemtuzumab
5. Positive anti-donor HLA antibodies against a mismatched allele in the selected donor
6. Low performance score: For MAC: Karnofsky Performance Score (KPS) < 70 percent, For NMA/RIC: <60 percent
7. High HCT-specific Comorbidity Index (HCT-CI): For MAC > 4, For NMA/RIC >6
8. Uncontrolled bacterial, viral or fungal infections (currently taking antimicrobial therapy and with progression or no clinical improvement) at time of enrollment
9. Seropositive for human immunodeficiency virus (HIV)-1 or -2, human T-lymphotropic virus (HTLV)-1 or -2 or Hepatitis B surface antigen (HbsAg) or anti-Hepatitis C virus (HCV) antibody (Ab)
10. Any uncontrolled autoimmune disease requiring active immunosuppressive treatment
11. Concurrent malignancies or active disease within 1 year, except non-melanoma skin cancers that have been curatively resected. Patients with concurrent indolent hematologic malignancies that do not require active treatment and are under active surveillance only (such as CLL, low-grade lymphomas, smoldering MM, MZL) may be included with the approval of Medical Monitor
12. History of idiopathic or secondary myelofibrosis
13. Women who are pregnant or breastfeeding

Study Design

Enrollment

300 participants

Anticipated

Allocation

Non randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: Arm A

Recipients with human leukocyte antigen (HLA)-identical related or unrelated or 1-allele mismatched (7/8 alleles) unrelated donor undergoing myeloablative conditioning (MAC); with single- or dual-agent graft-versus-host disease (GVHD) prophylaxis given

experimental: Arm B

Recipients with haploidentical-related donors undergoing MAC; with single- or dual-agent GVHD prophylaxis given

experimental: Arm C

Recipients with an HLA-identical related or unrelated donor undergoing MAC; no GVHD prophylaxis given

experimental: Arm D

Recipients with an HLA-identical related or unrelated donor undergoing non-myeloablative (NMA)/reduced intensity conditioning (RIC); with dual agent GVHD prophylaxis given

experimental: Arm E

Recipients with 1-allele mismatched (7/8 alleles) unrelated donor undergoing NMA/RIC; with dual-agent GVHD prophylaxis given

experimental: Arm F

Recipients with haploidentical-related donors undergoing NMA/RIC; with dual-agent GVHD prophylaxis given

Interventions

OrcaGraft (Orca-Q)

engineered donor allograft

Primary outcome measure

  • Dose Limiting Toxicities through Day +28 (dose escalation) [ Time Frame: 28 Days after administration of Orca-Q/OrcaGraft ]
  • Primary Graft failure through Day +28 (dose expansion) [ Time Frame: 28 Days after administration of Orca-Q/OrcaGraft ]

Central Contacts and Locations

Central contacts

Tamara Zharkevich, MD, PhD

650-246-9601info@orcabiosystems.com

James S McClellan, MD PhD

650-246-9601info@orcabiosystems.com

Locations

City of Hope

Recruiting

Duarte, California, United States, 91010

UC Davis

Recruiting

Sacramento, California, United States, 95817

Stanford Health Care

Recruiting

Stanford, California, United States, 94305

Moffitt Cancer Center

Recruiting

Tampa, Florida, United States, 33612

John Theurer Cancer Center at Hackensack University Medical Center

Recruiting

Hackensack, New Jersey, United States, 07601

Memorial Sloan Kettering Cancer Center

Recruiting

New York, New York, United States, 10065

University of Texas MD Anderson Cancer Center

Recruiting

Houston, Texas, United States, 77054

Fred Hutchinson Cancer Center

Recruiting

Seattle, Washington, United States, 98109

More Information

Sponsor

Orca Biosystems, Inc.

Last update posted

Jul 1, 2026

Last verified

Jun, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-08. This information was provided to ClinicalTrials.gov by Orca Biosystems, Inc. on 2026-07-01.