OtherAcceptedBeyond the letter
No nonclinical toxicology studies; safety supported by clinical data with a similar cell product
Why: Clinical safety data from a study with a similar cell product · Human data
“No toxicology studies were conducted for TREGZI. This omission is acceptable, as the applicant provided safety data from a Phase 1/2 clinical study with a similar clinical product to support initiation of the Phase 1b study”
✓ VerifiedFDA pharmacology/toxicology review, p. 36Source ↗ CarcinogenicityAcceptedBeyond the letter
No carcinogenicity/tumorigenicity studies with the cell product
Why: Not warranted based on product characteristics, biological activity and safety profile · Other reason
“No nonclinical studies were conducted to evaluate carcinogenicity/tumorigenicity of TREGZI.”
✓ VerifiedFDA pharmacology/toxicology review, p. 37Source ↗ “These studies are not warranted based on the product characteristics, biological activity, and safety profile.”
✓ VerifiedFDA pharmacology/toxicology review, p. 3Source ↗ BiodistributionAcceptedBeyond the letter
No cell distribution studies
Why: Product characteristics and biological activity, together with clinical safety data · Human data
“No nonclinical studies were conducted to evaluate cell distribution of TREGZI. Given the characteristics and biological activity of TREGZI, together with the clinical safety data for TREGZI, this omission is acceptable.”
✓ VerifiedFDA pharmacology/toxicology review, p. 36Source ↗ DARTAcceptedBeyond the letter
No developmental and reproductive toxicity studies
Why: Product characteristics and biological activity, together with clinical safety data · Human data
“DART Studies: No nonclinical studies were conducted to evaluate DART of TREGZI. Given the characteristics and biological activity TREGZI, together with the clinical safety data for TREGZI, this omission is acceptable.”
✓ VerifiedFDA pharmacology/toxicology review, p. 37Source ↗