About this trial
This is a phase 1, first-in-human (FIH), open-label, multicohort study to evaluate the safety, tolerability and preliminary efficacy of CLL1 or CD33 target Chimeric antigen receptor (CAR) -induced pluripotent stem cells derived NK cells in patients with relapsed/refractory AML
Eligibility criteria
Qualifiers
≥18 years old.
Confirmed diagnosis of r/r AML
CLL1 or CD33 expression is positive in AML blasts.
Eastern Cooperative Oncology Group (ECOG) performance status ≤1 and life expectancy greater than 12 weeks.
Disqualifiers
Allergic to drug used in this study.
History of allogeneic stem cell transplantation.
Received the vaccine within 4 weeks pror to the first infusion andor expected to reuire vaccination from the study period to 12 weeks ater the last intusion
Active central nervous system Leukemia.
Trial design
Treatments tested in this trial
- iPSC-NK cells
Treatment groups
Sponsors and collaborators
Zhejiang University
Lead sponsor
Hangzhou Qihanjiyin Biotech Co.,Ltd.
Collaborator