STN: 125646
Proper Name: tisagenlecleucel
Tradename: KYMRIAH
Manufacturer: Novartis Pharmaceuticals Corporation
Indication:
KYMRIAH is a CD19-directed genetically modified autologous T-cell immunotherapy indicated for the treatment of:
- Patients up to 25 years of age with B-cell precursor acute lymphoblastic leukemia (ALL) that is refractory or in second or later relapse.
- Adult patients with relapsed or refractory (r/r) large B-cell lymphoma after two or more lines of systemic therapy, including diffuse large B-cell lymphoma (DLBCL) not otherwise specified, high grade B-cell lymphoma and DLBCL arising from follicular lymphoma.
Limitations of Use: KYMRIAH is not indicated for treatment of patients with primary central nervous system lymphoma. - Adult patients with relapsed or refractory follicular lymphoma (FL) after two or more lines of systemic therapy. This indication is approved under accelerated approval based on response rate and duration of response. Continued approval for this indication may be contingent upon verification and description of clinical benefit in confirmatory trial(s).
Product Information
Supporting Documents
- August 16, 2024 Approval Letter – KYMRIAH
- June 13, 2024 Approval Letter – KYMRIAH
- April 12, 2024 Approval Letter – KYMRIAH
- May 26, 2022 Clinical Memo – KYMRIAH
- April 01, 2022 Statistical Review – KYMRIAH
- May 27, 2022 Approval Letter – KYMRIAH
- June 11, 2021 Approval Letter – KYMRIAH
- May 1, 2018 Approval Letter – KYMRIAH
- April 13, 2018 Summary Basis for Regulatory Action – KYMRIAH
- August 30, 2017 Approval Letter – KYMRIAH
- August 30, 2017 Summary Basis for Regulatory Action – KYMRIAH
- Approved Risk Evaluation and Mitigation Strategies (REMS) – KYMRIAH
- Approval History, Letters, Reviews and Related Documents – KYMRIAH
Related Information
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Content current as of:
09/03/2024