StudyFinder
MT2023-01:Safety and Efficacy of Expanded KIR-HLA Mismatched Natural Killer Cell Immunotherapy (AdaptNK) for High-Risk Myeloid Diseases as Bridge to Allogeneic Hematopoietic Stem Cell Transplantation
Status: Recruiting
The purpose of this study is to evaluate the safety of a new NK cell therapy for people with relapsed or treatment-resistant acute myeloid leukemia (AML). Participants will receive chemotherapy followed by an infusion of specially selected donor immune cells designed to help the body recognize and fight leukemia cells. Researchers will study the safety of this treatment, determine the most appropriate dose, and learn more about how the therapy works in the body.
Sex: Male or Female
Age Group: 18 years and over
Inclusion Criteria:
• diagnosis of acute myeloid leukemia (AML)
• adequate heart, lung, liver, and kidney function
• see link to clinicaltrials.gov for complete inclusion criteria
Exclusion Criteria:
• women who are pregnant or breast feeding
• diagnosed with leukemia involving the brain or spinal fluid
• active HIV, Hepatitis B, Hepatitis C, other serious infection, recent heart attack, or another active cancer requiring recent chemotherapy
• see link to clinicaltrials.gov for complete exclusion criteria
Interventions:
Biological: AdaptNK, Drug: Cyclophosphamide, Drug: Fludarabine, Drug: IL-2
Conditions:
Cancer
Keywords:
Clinics and Surgery Center (CSC), acute myeloid leukemia, AML
Study Contact: Alycia Lape-Krawczynski - lape0021@umn.edu
Principal Investigator: Mark Juckett
Phase: PHASE1
IRB Number: STUDY00027586
See this study on ClinicalTrials.gov