What this study is
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.
What's being tested
- OrcaGraft (Orca-Q)
Intervention · BIOLOGICAL
engineered donor allograft
Study details
- Official title
- A Phase 1 Dose Escalation and Expansion Study of Orca-Q, an Engineered Donor Graft Derived From Mobilized Peripheral Blood, in Recipients Undergoing Allogeneic Hematopoietic Cell Transplantation for Hematologic Malignancies
- Sponsor
- Orca Biosystems, Inc.
- Conditions
- Acute Myeloid Leukemia · Myelodysplastic Syndromes · Mixed Phenotype Acute Leukemia · Acute Lymphoblastic Leukemia
- Enrolling
- 300 people
- Starts
- 2019-04-08
- Est. completion
- 2027-12
- Design
- Open-label, non-randomized, parallel groups, Phase 1
- Record
- View on ClinicalTrials.gov ↗
Who can join
Age 12 Years – 78 YearsSex ALLHealthy volunteers Not acceptedYou may qualify if
- Age at the time of enrollment:; For MAC with fully matched donor (Arm A with 8/8 donor and Arm C) and NMA/RIC: Age ≥ 12 and ≤ 78 years; For MAC with mismatched donors (Arm A with 7/8 donor and Arm B): Age ≥ 12 and ≤ 65 years
- 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)
- Indicated for allogeneic hematopoietic stem cell transplant (alloHCT)
- Matched to a 8/8 or 7/8 related or unrelated donor, or to a related haploidentical donor
- Estimated glomerular filtration rate (eGFR) > 50 mL/minute (MAC with tacrolimus) or > 30 mL/minute (NMA/RIC or MAC without tacrolimus)
- Cardiac parameters: Cardiac ejection fraction ≥ 45 percent (MAC) or ≥ 40 percent (NMA/RIC)
- Diffusing capacity of the lung for carbon monoxide (DLCO) (adjusted for hemoglobin) ≥ 50 percent for MAC or ≥ 40 percent for NMA/RIC
- 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)
- Participants enrolling on NMA/RIC-alloHCT arms must be deemed unfit for a myeloablative alloHCT per assessment of the principal investigator (PI)
You can't join if
- Prior alloHCT
- 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
- Planned donor lymphocyte infusion (DLI)
- Planned pharmaceutical in vivo or ex vivo T cell depletion, e.g., post-transplant cyclophosphamide (Cy) or alemtuzumab
- Positive anti-donor HLA antibodies against a mismatched allele in the selected donor
- Low performance score: For MAC: Karnofsky Performance Score (KPS) < 70 percent, For NMA/RIC: <60 percent
- High HCT-specific Comorbidity Index (HCT-CI): For MAC > 4, For NMA/RIC >6
- Uncontrolled bacterial, viral or fungal infections (currently taking antimicrobial therapy and with progression or no clinical improvement) at time of enrollment
- 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)
- 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. 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
- History of idiopathic or secondary myelofibrosis
- Women who are pregnant or breastfeeding
Sign in and we'll check these against your records.Full criteria on ClinicalTrials.gov ↗
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Study locations (12)
9 openCity of Hope
Duarte, California, United States
- Amandeep Salhotra, MD · Contact
RecruitingUC Davis
Sacramento, California, United States
- Mehrdad Abedi, MD · Contact
RecruitingStanford Health Care
Stanford, California, United States
- Robert Lowsky, MD · Contact
RecruitingMoffitt Cancer Center
Tampa, Florida, United States
- Rawan Faramand, MD · Contact
RecruitingEmory University
Atlanta, Georgia, United States
- Edmund Waller, MD · Contact
RecruitingJohn Theurer Cancer Center at Hackensack University Medical Center
Hackensack, New Jersey, United States
- Siddhartha Reddy, MD · Contact
RecruitingMemorial Sloan Kettering Cancer Center
New York, New York, United States
- Roni Tamari, MD · Contact
RecruitingUniversity of Texas MD Anderson Cancer Center
Houston, Texas, United States
- Samer Srour, MD · Contact
RecruitingFred Hutchinson Cancer Center
Seattle, Washington, United States
- Boglarka Gyurkocza, MD · Contact
RecruitingThe University of Kansas Hospital
Kansas City, Kansas, United States
WithdrawnOhio State University
Columbus, Ohio, United States
Active, not recruitingFroedtert Memorial Lutheran Hospital
Milwaukee, Wisconsin, United States
Withdrawn
Study team
Sponsor
Orca Biosystems, Inc.
Study ID OGFT001-001
Study director
James S McClellan, MD, PhD
Orca Biosystems, Inc.
Frequently asked questions
The sponsor hasn't published answers to common questions for this trial.