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Recruiting Phase 1/2

Clinical Study of ARD103 CAR-T Therapy for Patients With R/R AML or MDS

NCT06680752 · tracked via the Priya Life Science USA tracker
Sponsor
ARCE Therapeutics, Inc
Phase
Phase 1/2
Started
2025-05-20
Last updated
2025-12-10

Condition(s) studied

Acute Myeloid Leukemia, in RelapseAcute Myeloid Leukemia RefractoryMDS (Myelodysplastic Syndrome)

Investigational drug(s) / intervention(s)

ARD103Cyclophosphamide →Fludarabine →

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)

FacilityCityRegionStatus
Novant Health Cancer Institute Charlotte North Carolina Recruiting
Novant Health Cancer Institute Winston-Salem North Carolina Recruiting
MD Anderson Cancer Center Houston Texas Recruiting

More ARCE Therapeutics, Inc. trials in the USA

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.

View NCT06680752 on ClinicalTrials.gov ↗ ← All trials in the USA