Clinical Study of ARD103 CAR-T Therapy for Patients With R/R AML or MDS
Condition(s) studied
Investigational drug(s) / intervention(s)
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
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 |
More ARCE Therapeutics, Inc. trials in the USA
Other trials for the same condition
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