Drug intelligence / Profile preview

ciltacabtagene autoleucel + 64Cu superparamagnetic iron oxide nanoparticle

Development stage
Phase 1
Lead developer
Legend Biotech
Modality
CAR-T Cells → Engineered T Cells → Adoptive Cell Transfer → Cell Therapies, Antibody-Radionuclide Conjugates → Antibody Conjugates → Antibody-Based Therapeutics, Beta-minus Emitters → Radiopharmaceuticals, Positron Emitters → Radiopharmaceuticals, Nanoparticles → Drug Delivery Systems
Administration
Intravenous
01

Overview

Ciltacabtagene autoleucel (cilta-cel) is a B-cell maturation antigen (BCMA)-directed, genetically modified autologous chimeric antigen receptor (CAR) T-cell therapy. It is approved for the treatment of adult patients with relapsed or refractory multiple myeloma who have received prior lines of therapy including a proteasome inhibitor, an immunomodulatory agent, and an anti-CD38 monoclonal antibody. The therapy involves collecting a patient’s own T cells, genetically modifying them to express a CAR targeting BCMA, and infusing them back into the patient to target and eliminate BCMA-expressing myeloma cells[5][7]. The combination "cilta-cel + 64Cu SPION" refers to labeling cilta-cel with copper-64-labeled superparamagnetic iron oxide nanoparticles (SPIONs), enabling dual PET/CT and MRI imaging for in vivo tracking of cell trafficking after infusion. This approach is being investigated in clinical trials for its ability to visualize the biodistribution of infused CAR-T cells in patients with advanced or extramedullary multiple myeloma[1][2][3]. Preclinical studies show that Cu-64 SPION labeling does not impair cilta-cel viability or function[2][3].

Brand names
CARVYKTI
Other names
cilta-cel + 64Cu SPIONciltacabtagene autoleucel + copper-64 superparamagnetic iron oxide nanoparticle
02

Targets

BCMA (B-cell maturation antigen)

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