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Phase I/II Clinical Study on Fully Human BCMA Chimeric Antigen Receptor Autologous T Cell Injection (CT103A) in the Treatment of Patients with Relapsed/refractory Multiple Myeloma

Trial Profile

Phase I/II Clinical Study on Fully Human BCMA Chimeric Antigen Receptor Autologous T Cell Injection (CT103A) in the Treatment of Patients with Relapsed/refractory Multiple Myeloma

Status: Recruiting
Phase of Trial: Phase I/II

Latest Information Update: 30 Mar 2025

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At a glance

  • Drugs Equecabtagene autoleucel (Primary) ; Cyclophosphamide; Fludarabine
  • Indications Multiple myeloma
  • Focus Adverse reactions; Pharmacodynamics; Registrational; Therapeutic Use
  • Acronyms FUMANBA-1
  • Sponsors IASO BioMed; Nanjing IASO Biotechnology; Nanjing IASO Biotherapeutics

Most Recent Events

  • 28 Mar 2025 According to an IASO BioMed Media Release, company announced that the Pharmaceutical Administration Bureau of the Macao Special Administrative Region (ISAF) has approved the New Drug Application (NDA) for Equecabtagene Autoleucel based on data from the pivotal FUMANBA-1 trial.
  • 27 Sep 2024 According to an IASO BioMed Media Release, the outcomes of relapsed/refractory multiple myeloma patients (n=91) with renal impairment (RI) treated with Equecabtagene-autoleucel in this study, were presented as a poster (Abstract Number: P-100) at the 2024 International Myeloma Society (IMS) Annual Meeting, on 26 Sep 2024 (UTC-3).
  • 12 Dec 2023 Results (n=88) presented at the 65th American Society of Hematology Annual Meeting and Exposition

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