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Anti-CD33-CLL1 CAR-T Cells (ICG415) for the Treatment of Relapsed/Refractory Acute Myeloid Leukemia
Bu çalışma, nükseden ya da dirençli akut miyeloid lösemi hastalarında, CD33 ve CLL1 olmak üzere iki hedefi birden tanıyan ICG415 CAR-T hücre tedavisini incelemektedir. Hücre infüzyonu öncesinde fludarabin ve siklofosfamid ile hazırlık tedavisi uygulanmaktadır. Çalışmaya 18-70 yaş arası hastalar alınmaktadır. Faz 1 aşamasında yürütülmekte ve katılımcı almaktadır.
Yukarıdaki özet, resmî kaydın sade dile aktarılmış halidir. Orijinal İngilizce başlık referans için gösterilir.
Kriterler ClinicalTrials.gov kaydından orijinal İngilizce haliyle alınmıştır. Uygunluk kararını yalnızca deneyi yürüten ekip verebilir.
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.