Abstract
The emergence of cell and gene therapies has dramatically changed the treatment paradigm in oncology and other therapeutic areas. Kymriah® (tisagenlecleucel), a CD19-directed genetically modified autologous T-cell immunotherapy, is currently approved in major markets for the treatment of relapsed/refractory (r/r) pediatric and young adult acute lymphoblastic leukemia, r/r diffuse large B-cell lymphoma, and r/r follicular lymphoma. This article presents a high-level overview of the clinical development journey of tisagenlecleucel, including its efficacy outcomes and safety considerations.
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Awasthi, R., Maier, H. J., Zhang, J., & Lim, S. (2023). Kymriah® (tisagenlecleucel)–An overview of the clinical development journey of the first approved CAR-T therapy. Human Vaccines and Immunotherapeutics, 19(1). https://doi.org/10.1080/21645515.2023.2210046
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