Not conducted (not warranted based on product characteristics and safety profile)
“Studies to evaluate the safety pharmacology, genotoxicity, and carcinogenicity of TUDRIQEV were not conducted.”
✓ VerifiedFDA summary basis for approval, p. 14Source ↗
Carcinogenicity
Not conducted (not warranted)
“Studies to evaluate the safety pharmacology, genotoxicity, and carcinogenicity of TUDRIQEV were not conducted.”
✓ VerifiedFDA summary basis for approval, p. 14Source ↗
Instead of carcinogenicity
Nothing submitted; studies considered not warranted based on product characteristics and safety profile
“Studies to evaluate the safety pharmacology, genotoxicity, and carcinogenicity of TUDRIQEV were not conducted. These studies are not warranted based on the product characteristics and safety profile.”
✓ VerifiedFDA summary basis for approval, p. 14Source ↗
Instead of genotoxicity
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.
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
Embryofetal study in pregnant rats (mRP1 IV, GD 4-16): no malformations or growth effects; minimal placental transfer
“no embryofetal structural abnormalities or adverse effects on embryofetal growth were observed following repeat IV mRP1 administration.”
✓ VerifiedFDA summary basis for approval, p. 13Source ↗
Safety pharmacology
Not conducted (not warranted)
“Studies to evaluate the safety pharmacology, genotoxicity, and carcinogenicity of TUDRIQEV were not conducted.”
✓ VerifiedFDA summary basis for approval, p. 14Source ↗
Genotox: Ames
Not conducted (not warranted)
“Studies to evaluate the safety pharmacology, genotoxicity, and carcinogenicity of TUDRIQEV were not conducted. These studies are not warranted based on the product characteristics and safety profile.”
✓ VerifiedFDA summary basis for approval, p. 14Source ↗
Genotox: in vitro mammalian
Not conducted (not warranted)
“Studies to evaluate the safety pharmacology, genotoxicity, and carcinogenicity of TUDRIQEV were not conducted. These studies are not warranted based on the product characteristics and safety profile.”
✓ VerifiedFDA summary basis for approval, p. 14Source ↗
Genotox: in vivo
Not conducted (not warranted)
“Studies to evaluate the safety pharmacology, genotoxicity, and carcinogenicity of TUDRIQEV were not conducted. These studies are not warranted based on the product characteristics and safety profile.”
✓ VerifiedFDA summary basis for approval, p. 14Source ↗
Carcinogenicity model
Not conducted (not warranted based on product characteristics and safety profile)
“Studies to evaluate the safety pharmacology, genotoxicity, and carcinogenicity of TUDRIQEV were not conducted. These studies are not warranted based on the product characteristics and safety profile.”
✓ VerifiedFDA summary basis for approval, p. 14Source ↗
Carcinogenicity timing
Not required (not warranted based on product characteristics and safety profile)
“Studies to evaluate the safety pharmacology, genotoxicity, and carcinogenicity of TUDRIQEV were not conducted. These studies are not warranted based on the product characteristics and safety profile.”
✓ VerifiedFDA summary basis for approval, p. 14Source ↗
hERG / QT
Not conducted (safety pharmacology not warranted)
“Studies to evaluate the safety pharmacology, genotoxicity, and carcinogenicity of TUDRIQEV were not conducted.”
✓ VerifiedFDA summary basis for approval, p. 14Source ↗
betibeglogene autotemcel · HBB T87Q (LVV, ex vivo HSC)
Insertional mutagenesis assessed instead of standard genotox: in vitro immortalization assay (low potential) and integration site analysis (no clonal dominance)