No immunotox/cytokine studies; literature shows anti-CD3-activated TIL cytotoxicity specific to autologous tumor, not heterologous targets
“Compared to TILs expanded in 1000 U/ml of IL-2 alone, TILs activated with anti-CD3 + 50 U/ml of IL-2 demonstrated higher cytotoxicity against autologous tumor cells but not against Daudi, K562, or histologically matched heterologous tumor cells.”
✓ VerifiedFDA pharmacology/toxicology review, p. 13Source ↗
Biodistribution & persistence
Not conducted; accepted based on known distribution of IV T cell products
“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 ↗
Modality-specific risk
Residual tumor cell contamination/tumorigenicity of tumor-derived product; LD chemo and IL-2 toxicity deferred to approved labels
“AMTAGVI specifications also include measures to control residual tumor cell levels in the final drug product.”
✓ VerifiedFDA pharmacology/toxicology review, p. 14Source ↗