Nonclinical precedent Request an invite
Precedia/Cell therapy/Tecelra/Skipped studies

Tecelra: genotox, carcinogenicity and repro: done or skipped?

afamitresgene autoleucel · MAGE-A4 TCR-T
Genotoxicity
Not conducted (no test models or relevant species); integration site analysis showed polyclonal products, no selective insertion
“Conventional genotoxicity studies were not conducted with afamitresgene autoleucel, due to the lack of appropriate test models and pharmacologically relevant species.”
✓ VerifiedFDA multi-discipline review, p. 40Source ↗
Carcinogenicity
Not conducted (no relevant animal models for human TCR-engineered T cells)
“Afamitresgene autoleucel is a human TCR engineered T-cell product, therefore conventional carcinogenicity studies were not performed due to the lack of relevant animal models.”
✓ VerifiedFDA multi-discipline review, p. 40Source ↗
Instead of carcinogenicity
Not stated in public reviews
Not reported in the public reviews. Reviewers summarise selectively, so this usually means it wasn't discussed publicly, not that it wasn't studied.
Instead of genotoxicity
Genomic insertion site analysis on products from five patients; no preferential integration near genes of concern
“A genomic insertion site analysis was performed on TECELRA products from five patients. There was no evidence for preferential integration near genes of concern.”
✓ VerifiedUS prescribing informationSource ↗
DRG histopathology
Not stated in public reviews
Not reported in the public reviews. Reviewers summarise selectively, so this usually means it wasn't discussed publicly, not that it wasn't studied.
Reproductive & developmental
Not conducted; theoretical testis/placenta risk (MAGE-A4 expression) judged mitigated by immune privilege, labeling, pharmacovigilance
“MAGE-A4 is known to be expressed in testes and placenta, and so there is a theoretical risk of embryotoxicity or toxicity to the testes.”
✓ VerifiedFDA multi-discipline review, p. 40Source ↗
Safety pharmacology
Not conducted; no relevant animal models
“No safety pharmacology studies were conducted, as there are no relevant animal models for the nonclinical safety assessment of afamitresgene autoleucel.”
✓ VerifiedFDA multi-discipline review, p. 39Source ↗
Genotox: Ames
Not conducted
“Conventional genotoxicity studies were not conducted with afamitresgene autoleucel, due to the lack of appropriate test models and pharmacologically relevant species.”
✓ VerifiedFDA multi-discipline review, p. 40Source ↗
Genotox: in vitro mammalian
Not conducted
“Conventional genotoxicity studies were not conducted with afamitresgene autoleucel, due to the lack of appropriate test models and pharmacologically relevant species.”
✓ VerifiedFDA multi-discipline review, p. 40Source ↗
Genotox: in vivo
Not conducted
“Conventional genotoxicity studies were not conducted with afamitresgene autoleucel, due to the lack of appropriate test models and pharmacologically relevant species.”
✓ VerifiedFDA multi-discipline review, p. 40Source ↗
Carcinogenicity model
Not conducted; vector integration site profile similar to other lentiviral products, no greater insertional oncogenesis risk expected
“However, vector integration site analysis demonstrated that the insertion site profile for the product was similar to other lentiviral vector products and was not expected to represent a greater risk for the development of insertional oncogenesis.”
✓ VerifiedFDA summary basis for approval, p. 13Source ↗
Carcinogenicity timing
Not conducted; no relevant animal models for a human TCR-engineered T-cell product
“Afamitresgene autoleucel is a human TCR engineered T-cell product, therefore conventional carcinogenicity studies were not performed due to the lack of relevant animal models.”
✓ VerifiedFDA multi-discipline review, p. 40Source ↗
hERG / QT
Not conducted (no relevant animal models for safety pharmacology)
“No safety pharmacology studies were conducted, as there are no relevant animal models for the nonclinical safety assessment of afamitresgene autoleucel.”
✓ VerifiedFDA multi-discipline review, p. 39Source ↗

Same question, other cell therapies

Abecma

idecabtagene vicleucel · BCMA CAR-T
Not conducted (traditional); insertion site analysis of 20 clinical lots

Alofisel

darvadstrocel · Allogeneic adipose MSC
Not conducted; cell-based product does not interact with DNA

Amtagvi

lifileucel · TIL therapy
Not conducted (not warranted given product characteristics and biological activity)

Aucatzyl

obecabtagene autoleucel · CD19 CAR-T
Not conducted (third-generation SIN lentiviral vector, release criterion, long-term clinical monitoring for insertional mutagenesis)

Breyanzi

lisocabtagene maraleucel · CD19 CAR-T
Not conducted (traditional); lentiviral integration site mapping instead

Carvykti

ciltacabtagene autoleucel · BCMA CAR-T
Not conducted (classical); lentiviral integration site analysis instead

ChondroCelect

characterised viable autologous cartilage cells · Autologous chondrocytes
Not conducted (per cell-based product guideline)

Ebvallo

tabelecleucel · EBV-specific allogeneic T cells
Not conducted (ICH S6(R1)); non-genetically engineered cells

Encelto

revakinagene taroretcel · CNTF (encapsulated RPE cell implant)
Done: ISO-10993 battery (bacterial, mammalian cell, mouse micronucleus on device extracts), negative

Gintuit

allogeneic cultured keratinocytes and fibroblasts in bovine collagen · Allogeneic keratinocytes + fibroblasts
Not conducted (nature of product and clinical experience)

Holoclar

autologous corneal epithelial cells containing limbal stem cells · Autologous limbal stem cells
Not conducted (classical); in vitro karyotype analysis of cells

Kymriah

tisagenlecleucel · CD19 CAR-T
Not conducted (classical); lentiviral integration site analysis on 14 donor products

Lantidra

donislecel · Allogeneic pancreatic islets
Not conducted

Laviv

azficel-T · Autologous fibroblasts
Not conducted (autologous nature, prior human experience)

MACI

autologous cultured chondrocytes on porcine collagen membrane · Autologous chondrocytes
Not conducted on cells; four studies on collagen membrane were non-mutagenic

Omisirge

omidubicel · Expanded cord blood HPC
No standard genotox; cytogenetic/karyotype analyses of CF and NF showed no clonal aneuploidy

Provenge

sipuleucel-T · PAP-GM-CSF (autologous APC)
Not conducted (autologous nature of product)

Rethymic

allogeneic processed thymus tissue · Allogeneic thymus tissue
Not conducted

Ryoncil

remestemcel-L · Allogeneic BM-MSC
Not conducted (not warranted)

Spherox

spheroids of autologous matrix-associated chondrocytes · Autologous chondrocyte spheroids
Not conducted (per cell-based product guideline)

StrataGraft

allogeneic cultured keratinocytes and dermal fibroblasts in murine collagen · Allogeneic keratinocytes + fibroblasts
Not conducted

Tecartus

brexucabtagene autoleucel · CD19 CAR-T
Not conducted (traditional); vector integration site analysis performed instead

Tregzi

allogeneic Treg immunotherapy with HSPC and T cells (Orca-T) · Allogeneic Treg + HSPC + Tcon
Not conducted

Yescarta

axicabtagene ciloleucel · CD19 CAR-T
Not conducted; literature review of retroviral-transduced T-cell transformation risk instead

Zalmoxis

allogeneic T cells modified with HSV-TK / dLNGFR (nalotimagene carmaleucel) · HSV-TK suicide-gene T cells
Not conducted; in vitro retroviral integration site analysis instead

Zemcelpro

dorocubicel · UM171-expanded cord blood CD34+
Done for residual UM171 only (Ames, CHO micronucleus negative) plus cytogenetics of treated cells; none for cells

Summary across all 27 cell therapies →