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
Latest Information Update: 29 Nov 2025
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
- 18 Sep 2025 According to IASO BioMed media release, 36-month long-term follow-up data were presented at the 2025 International Myeloma Society (IMS) Annual Meeting
- 18 Sep 2025 36-month long-term follow-up data from the FUMANBA-1 study published in the IASO BioMed Media Release
- 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.