Current CIBMTR Cell Therapy Studies

Company Novartis Kite Kite BMS/Celgene BMS/Celgene BMS/Celgene Janssen/Legend Adaptimmune
Product name Kymriah Yescarta Tecartus Breyanzi Abecma n/a Carvykti Tecelra
Scientific name Tisagenlecleucel Axicabtagene ciloleucel Brexucabtagene autoleucel Lisocabtagene maraleucel Idecabtagene vicleucel Non-conforming Liso-cel and Ide-cel Ciltacabtagene autoleucel Afamitresgene autoleucel
Other name CTL019 KTE-C19 KTE-X19 JCAR017 BB2121 JCAR017 & BB2121 BCMA n/a
FDA approval date 3/20/2017 (ALL)
5/1/2018 (DLBCL)
5/27/2022 (FL)
10/18/2017 7/24/2020 (MCL)
10/1/2021 (ALL)
2/5/2021 (DLBCL)
3/14/2024 (CLL)
5/15/2024 (FL)
5/30/2024 (MCL)
3/26/2021 n/a 2/28/2022 8/1/2024
Disease LYM
ALL
LYM
FL
Mantel cell LYM
ALL
LYM MM LYM
MM
MM Synovial sarcoma
Study ID SC17-08 SC17-07 CS20-03 SC18-04 SC19-10 CS20-36 SC19-09 CS21-177
Package insert Kymriah Yescarta Tecartus Breyanzi Abecma n/a Carvykti Tecelra
Reporting guide? Yes Yes Yes Yes Yes Yes Yes TBD

Enrollment into these cellular studies is done when the product name is reported on the F4000. No additional consent is required. These studies fall under the current CIBMTR Research Database consent form, which include HCT and cell therapy language.

Additional reporting guides are available for these studies on the CIBMTR Portal and contain extra information that is product specific and not part of the Forms Instruction Manuals. Some pages also contain recordings of the site initiation meetings.

Last modified: Mar 25, 2025