TECARTUS (brexucabtagene autoleucel)
STN: BL 125703
Proper Name: brexucabtagene autoleucel
Tradename: TECARTUS
Manufacturer: Kite Pharma, Inc.
Indication:
- Adult patients with relapsed or refractory mantle cell lymphoma (MCL). New Indication for this supplement: Adult patients with relapsed or refractory (r/r) B-cell
precursor acute lymphoblastic leukemia (ALL)
Product Information
- Package Insert - TECARTUS
- Demographic Subgroup Information - TECARTUS (brexucabtagene autoleucel)
Refer to Section 1.1 of the Clinical Review Memo for information about participation in the clinical trials and any analysis of demographic subgroup outcomes that is notable.
Supporting Documents
- October 1, 2021 Approval Letter - TECARTUS
- October 1, 2021 Clinical Pharmacology Memo - TECARTUS
- October 1, 2021 Clinical Review and Evaluation - TECARTUS
- Pharmacology/Toxicology Review - TECARTUS
- Statistical Review - TECARTUS
- February 24, 2021 Approval Letter - TECARTUS
- July 24, 2020 Approval Letter - TECARTUS
- July 23, 2020 Summary Basis for Regulatory Action - TECARTUS
- Approved Risk Evaluation and Mitigation Strategies (REMS) - TECARTUS
- Approval History, Letters, Reviews, and Related Documents - TECARTUS