Orca-T Expanded Access Program Study for Patients With Advanced Hematologic Malignancies

This study is not designed to test a hypothesis; rather, this study will provide patients with access to Orca-T if the commercial Orca-T product produced for them is deemed out of specification (OOS). Serious adverse events (SAEs) occurring during the safety reporting period (defined as the day the recipient receives the Orca-T HSPC drug product through day +365 after transplantation or until initiation of new anticancer therapy, whichever occurs sooner) will be reported.

NCT Number	NCT07346105
Lead Sponsor	Orca Biosystems, Inc.
Conditions	Hematologic Malignancies, Acute Myeloid Leukemia, Acute Lymphoid Leukemia, Myelodysplastic Syndrome, Mixed Phenotype Acute Leukemia
Updated on ClinicalTrials.gov	2026-07-24