This is a phase I/2, interventional, open-label, multicenter study to assess the safety and efficacy of ARD103 in patients with relapsed or refractory acute myeloid leukemia or myelodysplastic syndrome.
The investigational product (IP) for this study is ARD103, a C-type lectin-like molecule-1 (CLL-1) autologous chimeric antigen receptor T-cells (CAR-T). CLL-1 is highly expressed on both myeloid blasts and leukemia stem cells (LSCs) but is absent on normal hematopoietic stem cells (HSCs), suggesting CLL-1 as an excellent therapeutic target for AML and hence other potential myeloid malignancies.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
49
ARD103 autologous CAR-T cell therapy targeting CLL-1, single iv. infusion
iv administration for lymphodepletion
iv administration for lymphodepletion
Novant Health Cancer Institute
Charlotte, North Carolina, United States
RECRUITINGNovant Health Cancer Institute
Winston-Salem, North Carolina, United States
RECRUITINGMD Anderson Cancer Center
Houston, Texas, United States
RECRUITINGIncidence of Treatment-Emergent Adverse Events [Safety and Tolerability]
The records of AEs and severity following the first infusion of ARD103.
Time frame: 28 days post ARD103 infusion
To determine the RP2D of ARD103
RP2D of ARD103 following a 3+3 dose escalation schema (Phase 1)
Time frame: 28 days post ARD103 infusion
To evaluate overall response rate (ORR)
The ORR will be evaluated by European Leukemia Net (ELN) criteria
Time frame: Up to 24 months
Overall Survival (OS)
OS is defined as the time from ARD103 infusion to the date of death from any cause.
Time frame: First infusion date of ARD103 up to 15 years
Progression-free survival (PFS)
PFS is defined as the time from the infusion of ARD103 infusion to the first recorded response of disease progression, relapse, or death due to any cause, whichever occurs first.
Time frame: Up to 24 months
Time to best response
Time to best response is defined as the time from the infusion of ARD103 to the BOR.
Time frame: First infusion date of ARD103 up to 24 months
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