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Anti-CD33-CLL1 CAR-T Cells (ICG415) for the Treatment of Relapsed/Refractory Acute Myeloid Leukemia (ICG415-AML-01)

19 giugno 2026 aggiornato da: iCell Gene Therapeutics

A Clinical Study to Evaluate the Safety and Efficacy of ICG415 CAR-T Cells in Adult Patients With Relapsed/Refractory Acute Myeloid Leukemia

This single-arm, open-label phase I trial evaluates the safety and tolerability of ICG415, autologous CAR-T cells targeting CD33 and CLL1, in patients with relapsed or refractory acute myeloid leukemia (AML). Subjects receive lymphodepleting chemotherapy followed by autologous CAR-T infusion. The primary goal is to assess safety and preliminary anti-leukemic efficacy in patients failing standard AML therapies.

Panoramica dello studio

Descrizione dettagliata

Acute myeloid leukemia (AML) is an aggressive hematologic malignancy with limited treatment options for patients who are relapsed or refractory (R/R) to standard therapies. Leukemic blasts in R/R AML frequently co-express CD33 and CLL1, while sparing normal hematopoietic stem cells, making them rational targets for chimeric antigen receptor (CAR) T-cell therapy.

This phase I, single-arm, open-label study evaluates ICG415 CAR-T Cells in patients with R/R AML. After leukapheresis and ex vivo modification, patients receive a single CAR-T cell infusion following lymphodepleting chemotherapy with fludarabine and cyclophosphamide. Primary objectives are safety and tolerability, including dose-limiting toxicities (DLTs), cytokine release syndrome (CRS), and neurological events. Secondary objectives include response rate (CR/CRi/PR), minimal residual disease (MRD) negativity, progression-free survival (PFS), and overall survival (OS).

All participants will be followed for up to 24 months with regular clinical, laboratory, and imaging evaluations to monitor both treatment efficacy and potential complications.

Tipo di studio

Interventistico

Iscrizione (Stimato)

18

Fase

  • Fase 1

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Backup dei contatti dello studio

Luoghi di studio

    • Jiangxi
      • Nanchang, Jiangxi, Cina, 330006
        • Reclutamento
        • Jiangxi Provincial People's Hospital (Participating Site)
        • Contatto:
      • Nanchang, Jiangxi, Cina, 330006
        • Reclutamento
        • The First Affiliated Hospital of Nanchang University (Lead Site)
        • Contatto:

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

No

Descrizione

Inclusion Criteria:

  1. Written informed consent approved by IRB/IEC obtained from subject or legally authorized representative prior to any screening procedures.
  2. Age ≥ 18 years and ≤ 70 years at the time of informed consent signing.
  3. Diagnosis of acute myeloid leukemia (AML) per 2022 WHO Classification, meeting criteria for relapsed/refractory (R/R) AML as defined in the Chinese Guidelines for the Diagnosis and Management of Relapsed/Refractory Acute Myeloid Leukemia (2023 Edition): Relapsed AML: Reappearance of leukemic blasts in peripheral blood, bone marrow blasts ≥5%, or extramedullary leukemic infiltration after complete remission (CR). Refractory AML: failure to achieve CR after two cycles of standard induction chemotherapy; early relapse within 12 months post-CR; late relapse with salvage chemotherapy resistance; ≥2 disease relapses or persistent extramedullary disease.
  4. Bone marrow leukemic blasts positive for both CLL-1 and CD33 by flow cytometry.
  5. If circulating blasts are detectable at screening, tumor cell surface immunophenotype must be CD4 and CD8 double-negative by flow cytometry.
  6. ECOG performance status 0-2.
  7. Expected overall survival > 3 months.
  8. Females of childbearing potential: negative serum pregnancy test and effective contraception for 1 year post-infusion. Males of reproductive potential: effective barrier contraception for 1 year post-infusion and no sperm donation within 1 year after infusion.

Exclusion Criteria:

  1. Prior receipt of CAR-T cell therapy or other genetically modified cell therapy prior to informed consent.
  2. Severe major organ dysfunction: Renal: eGFR < 50 mL/min (Cockcroft-Gault); Hepatic: ALT/AST > 3 × ULN (>5×ULN if disease-related), total bilirubin > 2 × ULN (>3×ULN for Gilbert syndrome); Cardiac: LVEF < 50%, room air SpO₂ <94%, uncontrolled severe cardiac disease.
  3. Active uncontrolled infection: positive HBsAg/HBV-DNA, active HCV-RNA positivity, HIV positive, positive syphilis antibody, active uncontrolled EBV or CMV viremia.
  4. Unstable severe systemic disease requiring continuous medication.
  5. Grade >2 bleeding within 30 days before screening or chronic long-term anticoagulant treatment.
  6. Uncontrolled life-threatening bacterial, fungal or viral infection.
  7. Non-leukemic central nervous system organic disease or active CNS-2/CNS-3 leukemia; previously treated and resolved CNS leukemia is permitted.
  8. Concurrent other malignant tumor except cured in-situ carcinoma or malignancies with ≥5 years continuous complete remission.
  9. Live-attenuated vaccines within 30 days before screening or planned within 3 months after CAR-T infusion.
  10. Received any other investigational medicinal product within 3 months prior to ICF signature.
  11. Allogeneic hematopoietic stem cell transplantation within 6 months before screening.
  12. Pregnant or breastfeeding women.
  13. Suicidal tendency, ongoing alcohol or illicit drug dependence.
  14. Known hypersensitivity to investigational product, excipients or concomitant drugs.
  15. Any other condition judged inappropriate for trial entry by investigator.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: N / A
  • Modello interventistico: Assegnazione sequenziale
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Single Arm, Anti-CD33-CLL1 CAR-T (ICG415) for Relapsed or Refractory AML
Anti-CD33, Anti-CLL1 Compound CAR-T Cells

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Incidence of Dose-Limiting Toxicities (DLTs)
Lasso di tempo: Within 28 days after ICG415 CAR-T cell infusion
DLTs assessed according to the protocol-defined criteria.
Within 28 days after ICG415 CAR-T cell infusion
Incidence and Severity of Treatment-Emergent Adverse Events (TEAEs)
Lasso di tempo: From first dose through 24 months post infusion
Frequency and severity of TEAEs graded by NCI-CTCAE Version 5.0, including changes from baseline in vital signs, physical examination, 12-lead ECG, and clinical laboratory parameters (complete blood count, urinalysis, blood chemistry, coagulation function, etc.).
From first dose through 24 months post infusion

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Objective Response Rate (ORR) at Months 1, 3, and 6
Lasso di tempo: Month 1, Month 3, Month 6
ORR defined as proportion of subjects achieving complete remission (CR), complete remission with incomplete count recovery (CRi), or complete remission with partial hematological recovery (CRh) per response criteria.
Month 1, Month 3, Month 6
Rates of CR, CRi, and PR at Year 1 and Year 2
Lasso di tempo: Year 1, Year 2
Proportion of subjects achieving complete remission (CR), complete remission with incomplete count recovery (CRi), and partial remission (PR) at 1 and 2 years post infusion.
Year 1, Year 2
Cumulative Incidence of Relapse (CIR) at Year 1 and Year 2
Lasso di tempo: Year 1, Year 2
Cumulative incidence of disease relapse at 1 and 2 years after CAR-T cell infusion.
Year 1, Year 2
Duration of Response (DOR)
Lasso di tempo: From first documented response to disease relapse or death from any cause, assessed up to 24 months
Time from first objective response (CR, CRi, or CRh) to relapse or death, whichever occurs first.
From first documented response to disease relapse or death from any cause, assessed up to 24 months
Progression-Free Survival (PFS)
Lasso di tempo: From date of infusion to disease progression or death from any cause, assessed up to 24 months
Time from ICG415 infusion to disease progression (relapse or treatment failure) or death from any cause.
From date of infusion to disease progression or death from any cause, assessed up to 24 months
Overall Survival (OS)
Lasso di tempo: From date of infusion to death from any cause, assessed up to 24 months
Time from ICG415 infusion to death from any cause.
From date of infusion to death from any cause, assessed up to 24 months
Event-Free Survival (EFS)
Lasso di tempo: From date of infusion to any treatment failure, relapse, or death, assessed up to 24 months
Time from ICG415 infusion to any event including lack of response, disease relapse, or death from any cause.
From date of infusion to any treatment failure, relapse, or death, assessed up to 24 months
CAR-T Cell Kinetics - Persistence over Time
Lasso di tempo: Days 0, 4, 7, 14, 21, 28; Months 2, 3, 6, 9, 12, 18, 24
Number and duration of detectable CAR-T cells in peripheral blood. Testing stops after two consecutive negative results.
Days 0, 4, 7, 14, 21, 28; Months 2, 3, 6, 9, 12, 18, 24
Cytokine Level Changes
Lasso di tempo: Days 0, 7, 14, 21, 28; Months 2, 3, 6
Changes in serum cytokine levels including IL-6, IL-10, IL-15, TNF-α, and IFN-γ.
Days 0, 7, 14, 21, 28; Months 2, 3, 6
Peripheral Blood Lymphocyte Subset Changes
Lasso di tempo: Days 0, 7, 14, 21, 28; Months 2, 3, 6
Changes in lymphocyte subsets including T cells, B cells, NK cells, and CD4/CD8 ratio measured by flow cytometry.
Days 0, 7, 14, 21, 28; Months 2, 3, 6
Anti-Drug Antibody (ADA) Levels
Lasso di tempo: Day 28; Months 3, 6, 12
Incidence and titers of anti-drug antibodies (ADA) against ICG415 CAR-T cells.
Day 28; Months 3, 6, 12

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

10 giugno 2026

Completamento primario (Stimato)

4 luglio 2028

Completamento dello studio (Stimato)

4 luglio 2029

Date di iscrizione allo studio

Primo inviato

19 giugno 2026

Primo inviato che soddisfa i criteri di controllo qualità

19 giugno 2026

Primo Inserito (Effettivo)

25 giugno 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

25 giugno 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

19 giugno 2026

Ultimo verificato

1 giugno 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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