Acute Myeloid Leukemia, in RelapseAcute Myeloid Leukemia RefractoryMDS (Myelodysplastic Syndrome)
Investigational drug(s) / intervention(s)
ARD103CyclophosphamideFludarabine
ARD103: ARD103 autologous CAR-T cell therapy targeting CLL-1, single iv. infusion
Cyclophosphamide: iv administration for lymphodepletion
Fludarabine: iv administration for lymphodepletion
Study summary
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.
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria:
* Documented diagnosis of AML with either refractory or relapsed disease or diagnosis of MDS and ≥ 5% BM blasts
* Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
* Adequate hematologic status:
* Absolute lymphocyte count (ALC) \> 100/mm3
* Adequate renal, hepatic, cardiac and pulmonary function:
* ALT and AST \< 3.0 × the ULN
* Creatinine clearance ≥ 45.0 mL/min as estimated by Cockcroft-Gault and independent dialysis
* Total bilirubin ≤ 2.0 mg/dL
* Pregnancy testing: females of childbearing potential must have a negative serum or urine pregnancy test
* Contraception: males and females of childbearing potential must agree to use an effective method of contraception
* Participant is capable of giving signed informed consent
Exclusion Criteria:
* Participants with acute promyelocytic leukemia
* Presence of active and clinically relevant central nervous system (CNS) disorder
* Autoimmune disease requiring immunosuppressive treatment
* Participants with known hepatic bridging cirrhosis
* Currently active infection with hepatitis B or C
* Previous treatment with investigational gene or cell therapy (including CAR therapy)
* Any active acute GvHD or systemic treatment of more than 10 mg prednisone daily (or equivalent)
* Previous chemotherapy including biologic/targeted therapy or immunological agents directed to the pathology within 14 days prior to screening and all along the study duration
Primary outcome measure(s)
Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability] — 28 days post ARD103 infusion The records of AEs and severity following the first infusion of ARD103.
To determine the RP2D of ARD103 — 28 days post ARD103 infusion RP2D of ARD103 following a 3+3 dose escalation schema (Phase 1)
To evaluate overall response rate (ORR) — Up to 24 months The ORR will be evaluated by European Leukemia Net (ELN) criteria
Trial sites (3)
Facility
City
Region
Status
Novant Health Cancer Institute
Charlotte
North Carolina
Recruiting
Novant Health Cancer Institute
Winston-Salem
North Carolina
Recruiting
MD Anderson Cancer Center
Houston
Texas
Recruiting
Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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