FDA Approves Tisagenlecleucel for B-Cell ALL and Tocilizumab for Cytokine Release Syndrome

Aug 29

2017

The U.S. Food and Drug Administration granted regular approval to tisagenlecleucel (KYMRIAH®, Novartis Pharmaceuticals Corp.) for the treatment of patients up to age 25 years with B-cell precursor acute lymphoblastic leukemia (ALL) that is refractory or in second or later relapse.

Citations

APA

American Society of Hematology. (2017).
FDA Approves Tisagenlecleucel for B-Cell ALL and Tocilizumab for Cytokine Release Syndrome.
Retrieved from https://www.hematology.org/education/clinicians/drug-resources/fda-alerts/2017/fda-approves-tisagenlecleucel-for-b-cell-all-and-tocilizumab-for-cytokine-release-syndrome.

Chicago

American Society of Hematology.
"FDA Approves Tisagenlecleucel for B-Cell ALL and Tocilizumab for Cytokine Release Syndrome." Hematology.org.
https://www.hematology.org/education/clinicians/drug-resources/fda-alerts/2017/fda-approves-tisagenlecleucel-for-b-cell-all-and-tocilizumab-for-cytokine-release-syndrome
(label-accessed December 15, 2024).

MLA

"American Society of Hematology."
FDA Approves Tisagenlecleucel for B-Cell ALL and Tocilizumab for Cytokine Release Syndrome, 15 Dec. 2024 ,
https://www.hematology.org/education/clinicians/drug-resources/fda-alerts/2017/fda-approves-tisagenlecleucel-for-b-cell-all-and-tocilizumab-for-cytokine-release-syndrome.

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