A Clinical Study to Investigate the Safety and Efficacy of CT1390B in Patients With Relapsed/Refractory Acute Myeloid Leukemia
CT1390B is positioned to address a significant unmet need in the treatment of relapsed/refractory acute myeloid leukemia (AML), particularly among patients who are CLL-1 positive. The trial is sponsored by the Institute of Hematology & Blood Diseases Hospital in China, indicating a strong local expertise in hematological malignancies. The market for AML therapies is competitive, with several CAR-T therapies in development; however, CT1390B's unique targeting of CLL-1 may provide a differentiated approach. Given the estimated enrollment of 9-18 participants, the trial's results could have implications for future development and partnerships, particularly if safety and efficacy are demonstrated. The trial is not yet recruiting, with an estimated start date in March 2026, which may affect the timeline for potential market entry.
Indication: Relapsed/Refractory Acute Myeloid Leukemia(AML)
Modality: cell therapy
Target: CLL-1 positive cells in relapsed/refractory acute myeloid leukemia (AML)
Sponsor: Institute of Hematology & Blood Diseases Hospital, China
Source URL: ClinicalTrials.gov
Source updated: Mar 02, 2026
Ingested: Jun 16, 2026
Model: trialsignal-ai-v1
Validation: validated
Matched by target_normalized: CLL-1 positive cells in relapsed/refractory acute myeloid leukemia (AML)
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Condition raw: Relapsed/Refractory Acute Myeloid Leukemia(AML)
Condition normalized: Relapsed/Refractory Acute Myeloid Leukemia(AML)
Modality raw: cell therapy
Modality normalized: cell therapy
Target raw: CLL-1 positive cells in relapsed/refractory acute myeloid leukemia (AML)
Target normalized: CLL-1 positive cells in relapsed/refractory acute myeloid leukemia (AML)