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 ↗