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Amtagvi: what flexibility did regulators accept, and why?

lifileucel · TIL therapy
Flexibility accepted
Efficacy modelQuestioned
No nonclinical pharmacology studies with the product; published data on similar murine and human tumor-derived T lymphocytes cited instead
“No nonclinical studies were conducted with AMTAGVI. Instead, the applicant cited published nonclinical data evaluating similar murine and human tumor-derived T lymphocytes to provide support for AMTAGVI.”
✓ VerifiedFDA pharmacology/toxicology review, p. 2Source ↗
“The GEN2 manufacturing process for AMTAGV1 is different from the TILs expansion method in this publication. Therefore, this reviewer cannot comment on whether AMTAGV1 exhibits comparable cytotoxicity against autologous tumor cells as TILs in this publication.”
✓ VerifiedFDA pharmacology/toxicology review, p. 12Source ↗
OtherAcceptedBeyond the letter
No toxicology studies of any kind
Why: Characteristics and biological activity of the product · Low-risk modality
“No toxicology studies were conducted for AMTAGVI. Given the characteristics and biological activity of AMTAGVI, this omission is acceptable.”
✓ VerifiedFDA pharmacology/toxicology review, p. 13Source ↗
BiodistributionAcceptedBeyond the letter
No cell distribution studies
Why: Available information on in vivo distribution of intravenously administered T cell products · Class precedent
“No nonclinical studies were conducted to evaluate distribution of AMTAGVI. Based on the available information on the in vivo distribution of intravenously administered T cell products, this omission is acceptable.”
✓ VerifiedFDA pharmacology/toxicology review, p. 13Source ↗
CarcinogenicityAcceptedBeyond the letter
No tumorigenicity studies
Why: Published studies showed expanded human TIL cultures were free of tumor cells · Weight of evidence
“No tumorigenicity studies were conducted for AMTAGVI. This is acceptable since Studies #3 and #4 provided evidence that the expanded human TIL cultures in the studies were free of tumor cells.”
✓ VerifiedFDA pharmacology/toxicology review, p. 14Source ↗
DARTAcceptedBeyond the letter
No DART, genotoxicity or safety pharmacology studies
Why: Characteristics and biological activity of the product · Low-risk modality
“No DART studies were conducted for AMTAGVI. Given the characteristics and biological activity of AMTAGVI, this omission is acceptable.”
✓ VerifiedFDA pharmacology/toxicology review, p. 14Source ↗

Same question, other cell therapies

Abecma

idecabtagene vicleucel · BCMA CAR-T
No single or repeat-dose in vivo toxicity studies; no appropriate animal model for autologous human CAR-T cells

Alofisel

darvadstrocel · Allogeneic adipose MSC
No reproductive and developmental toxicity studies

Aucatzyl

obecabtagene autoleucel · CD19 CAR-T
No general toxicity studies; no pharmacologically relevant species for human CAR T cells

Breyanzi

lisocabtagene maraleucel · CD19 CAR-T
No pharmacologically relevant species; no conventional single- or repeat-dose toxicity, local tolerance or other traditional studies

Carvykti

ciltacabtagene autoleucel · BCMA CAR-T
No GLP-compliant formal toxicology studies and no repeat-dose study; no relevant animal species

ChondroCelect

characterised viable autologous cartilage cells · Autologous chondrocytes
All nonclinical studies non-GLP, run as combined pharmacodynamic/distribution/toxicity studies in nude mice, sheep and goats

Ebvallo

tabelecleucel · EBV-specific allogeneic T cells
No single- or repeat-dose toxicity studies; no relevant animal model for an HLA-restricted human T-cell product

Encelto

revakinagene taroretcel · CNTF (encapsulated RPE cell implant)
No carcinogenicity/tumorigenicity studies; waived on toxicological risk assessments of rhCNTF and residual medium

Gintuit

allogeneic cultured keratinocytes and fibroblasts in bovine collagen · Allogeneic keratinocytes + fibroblasts
ICH toxicology package (chronic toxicity, genotoxicity, carcinogenicity, DART, safety pharmacology, immunotoxicity) not conducted; partly covered by device biocompatibility testing

Holoclar

autologous corneal epithelial cells containing limbal stem cells · Autologous limbal stem cells
No in vivo toxicity studies (single dose, repeat dose, immunogenicity); no suitable animal model

Kymriah

tisagenlecleucel · CD19 CAR-T
No single-dose or standard toxicity studies: patient-specific human cell product cannot be given to immunocompetent animals

Lantidra

donislecel · Allogeneic pancreatic islets
No nonclinical studies with the product; published islet-transplant literature in rodents and monkeys relied on instead

Laviv

azficel-T · Autologous fibroblasts
No preclinical studies of any kind with the product; relied on prior commercial human use and published literature

MACI

autologous cultured chondrocytes on porcine collagen membrane · Autologous chondrocytes
No carcinogenicity/tumorigenicity studies

Omisirge

omidubicel · Expanded cord blood HPC
In vivo studies described as GLP lacked QA statements, facility information and deviation reports

Provenge

sipuleucel-T · PAP-GM-CSF (autologous APC)
No conventional toxicology or pharmacokinetic studies; risk-based approach justification instead

Rethymic

allogeneic processed thymus tissue · Allogeneic thymus tissue
No nonclinical toxicology studies: no relevant animal species or model

Ryoncil

remestemcel-L · Allogeneic BM-MSC
Nonclinical studies used surrogate animal-derived MSC and human MSC from an early manufacturing process, not the commercial product

Spherox

spheroids of autologous matrix-associated chondrocytes · Autologous chondrocyte spheroids
No long-term toxicity data: pivotal 9-month GLP sheep study failed through loss of the implants

StrataGraft

allogeneic cultured keratinocytes and dermal fibroblasts in murine collagen · Allogeneic keratinocytes + fibroblasts
Toxicity assessed only in immunodeficient mice, with significant study design and data limitations

Tecartus

brexucabtagene autoleucel · CD19 CAR-T
No relevant animal model; no GLP formal toxicology studies, only safety observations in a syngeneic mouse surrogate model

Tecelra

afamitresgene autoleucel · MAGE-A4 TCR-T
No in vivo single- or repeat-dose toxicity studies; no appropriate animal model for human TCR-engineered T cells

Tregzi

allogeneic Treg immunotherapy with HSPC and T cells (Orca-T) · Allogeneic Treg + HSPC + Tcon
No nonclinical toxicology studies; safety supported by clinical data with a similar cell product

Yescarta

axicabtagene ciloleucel · CD19 CAR-T
No toxicology studies with the product; no relevant animal model, murine surrogate CAR-T used for pharmacology

Zalmoxis

allogeneic T cells modified with HSV-TK / dLNGFR (nalotimagene carmaleucel) · HSV-TK suicide-gene T cells
No conventional toxicology studies; safety read from two immunodeficient-mouse GvHD pharmacology models

Zemcelpro

dorocubicel · UM171-expanded cord blood CD34+
UM171 toxicity studies in rats (single dose) and monkeys (three doses) not GLP-compliant

Summary across all 27 cell therapies →