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.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
300
engineered donor allograft
City of Hope
Duarte, California, United States
RECRUITINGUC Davis
Sacramento, California, United States
RECRUITINGDose Limiting Toxicities through Day +28 (dose escalation)
Safety and tolerability of Orca-Q (formerly OrcaGraft) in adults undergoing myeloablative allogeneic hematopoietic cell transplantation (MA-alloHCT) will be evaluated by identification of the following dose limiting toxicities: Grade ≥ 3 infusion-related reaction or cytokine release syndrome, Grade ≥ 3 acute GVHD, Any Grade ≥ 3 treatment-related non-hematologic event not clearly related to the underlying malignancy, intercurrent infection, the HCT conditioning regimen, or other pre-existing medical condition
Time frame: 28 Days after administration of Orca-Q/OrcaGraft
Primary Graft failure through Day +28 (dose expansion)
Primary graft failure in the dose expansion phase, defined as being alive without recovery of neutrophils during the evaluation period
Time frame: 28 Days after administration of Orca-Q/OrcaGraft
Neutrophil Engraftment through Day +28
Neutrophil engraftment defined as an absolute neutrophil count of \>/=500/mm3 for 3 consecutive days
Time frame: 28 days after administration of Orca-Q/OrcaGraft
Platelet Engraftment through Day +50
Platelet engraftment is defined as achieving a platelet count \> 20,000/mm3 for 3 consecutive days without platelet transfusion in the preceding 7 days, by Day +50
Time frame: 50 days after administration of Orca-Q/OrcaGraft
Secondary Graft Failure through Day +100
Secondary graft failure is defined as neutrophil engraftment followed by subsequent decline in absolute neutrophil counts \< 500 cells/μL, unresponsive to growth factor therapy, by Day +100
Time frame: 100 days after administration of Orca-Q/OrcaGraft
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Stanford Health Care
Stanford, California, United States
RECRUITINGMoffitt Cancer Center
Tampa, Florida, United States
RECRUITINGEmory University
Atlanta, Georgia, United States
ACTIVE_NOT_RECRUITINGThe University of Kansas Hospital
Kansas City, Kansas, United States
WITHDRAWNMemorial Sloan Kettering Cancer Center
New York, New York, United States
RECRUITINGOhio State University
Columbus, Ohio, United States
ACTIVE_NOT_RECRUITINGUniversity of Texas MD Anderson Cancer Center
Houston, Texas, United States
RECRUITINGFred Hutchinson Cancer Center
Seattle, Washington, United States
RECRUITING...and 1 more locations
Acute GVHD through Day +100
Acute GVHD will be staged and graded per Mount Sinai Acute GvHD International Consortium (MAGIC) Standardization criteria
Time frame: 100 days after administration of Orca-Q/OrcaGraft
Chronic GVHD through Day +365
Chronic GVHD will be diagnosed per 2014 International NIH Chronic GVHD Diagnosis and Staging Consensus Working Group criteria
Time frame: 365 days after administration of Orca-Q/OrcaGraft
Incidence of Non-relapse Mortality (NRM) through Day +365
NRM is defined as death without evidence of disease recurrence
Time frame: 365 days after administration of Orca-Q/OrcaGraft
Incidence of Disease Relapse through Day +365
Recurrence of primary disease for transplant
Time frame: 365 days after administration of Orca-Q/OrcaGraft
GVHD-free and Relapse-free Survival (GRFS) through Day +365
Survival free from GVHD and relapse
Time frame: 365 days after administration of Orca-Q/OrcaGraft
Disease-free Survival (DFS) through Day +365
DFS is the time from date of transplant to death or relapse, whichever comes first.
Time frame: 365 days after administration of Orca-Q/OrcaGraft
Overall Survival through Day +365
OS is defined as the time from the date of transplant to the date of death from any cause or, for surviving patients, to the date of last follow-up.
Time frame: 365 days after administration of Orca-Q/OrcaGraft