Study Evaluating Safety and Efficacy of UCART123v1.2 in Patients With Relapsed/Refractory Acute Myeloid Leukemia (AMELI-01)
Phase I, Open Label Dose Escalation and Dose-Expansion Study to Evaluate the Safety, Expansion, Persistence, and Clinical Activity of UCART123 (Allogeneic Engineered T-cells Expressing Anti-CD123 Chimeric Antigen Receptor), Administered in Patients With Relapsed/Refractory Acute Myeloid Leukemia
Sponsor: Cellectis S.A.
This PHASE1 trial investigates Relapsed/Refractory Acute Myeloid Leukemia and is currently ongoing. Cellectis S.A. leads this study, which shows 19 recorded versions since 2017 — indicating substantial longitudinal coverage. As an oncology study, it adds to the longitudinal record of treatment development for this indication.
Status Flow
Change History
19 versions recorded-
Sep 2025 — Present [monthly]
Active Not Recruiting PHASE1
Status: Recruiting → Active Not Recruiting
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Sep 2024 — Sep 2025 [monthly]
Recruiting PHASE1
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Jul 2024 — Sep 2024 [monthly]
Recruiting PHASE1
-
Mar 2024 — Jul 2024 [monthly]
Recruiting PHASE1
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Jul 2022 — Mar 2024 [monthly]
Recruiting PHASE1
▶ Show 14 earlier versions
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Oct 2021 — Jul 2022 [monthly]
Recruiting PHASE1
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Jun 2021 — Oct 2021 [monthly]
Recruiting PHASE1
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Apr 2021 — Jun 2021 [monthly]
Recruiting PHASE1
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Mar 2021 — Apr 2021 [monthly]
Recruiting PHASE1
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Jan 2021 — Mar 2021 [monthly]
Recruiting PHASE1
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Jun 2020 — Jan 2021 [monthly]
Recruiting PHASE1
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Jan 2020 — Jun 2020 [monthly]
Recruiting PHASE1
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Jun 2019 — Jan 2020 [monthly]
Recruiting PHASE1
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Jan 2019 — Jun 2019 [monthly]
Recruiting PHASE1
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Jun 2018 — Jan 2019 [monthly]
Recruiting PHASE1
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Apr 2018 — Jun 2018 [monthly]
Recruiting PHASE1
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Jan 2018 — Apr 2018 [monthly]
Recruiting PHASE1
Status: Suspended → Recruiting
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Oct 2017 — Jan 2018 [monthly]
Suspended PHASE1
Status: Recruiting → Suspended
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Jul 2017 — Oct 2017 [monthly]
Recruiting PHASE1
First recorded
Jun 2017
Trial started
Per CT.gov start date — pre-dates our first snapshot
Eligibility Summary
No eligibility information available.
Contact Information
- Cellectis S.A.
For direct contact, visit the study record on ClinicalTrials.gov .