Not conducted; not warranted for a biotechnology-derived product
“No genetic toxicology or carcinogenicity studies were conducted or warranted to support this BLA submission, as dostarlimab‐gxly is a biotechnology‐derived pharmaceutical and the proposed indication is for advanced cancer.”
✓ VerifiedFDA multi-discipline review, p. 37Source ↗
Carcinogenicity
Not conducted (biotechnology product for advanced cancer)
“No genetic toxicology or carcinogenicity studies were conducted or warranted to support this BLA submission, as dostarlimab‐gxly is a biotechnology‐derived pharmaceutical and the proposed indication is for advanced cancer.”
✓ VerifiedFDA multi-discipline review, p. 37Source ↗
Instead of carcinogenicity
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.
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
No dedicated studies; literature: PD-L1 blockade in murine pregnancy models disrupts fetal tolerance and increases fetal loss
“Blockade of PD-L1 signaling has been shown in murine models of pregnancy to disrupt tolerance to the foetus and to result in an increase in foetal loss.”
Incorporated into 4-week monkey study; no effects on CV, respiratory or CNS function up to 100 mg/kg
“The administration of dostarlimab by a weekly IV dose for 4 weeks (5 total doses) to cynomolgus monkeys at dose levels of 0, 10, 30, or 100 mg/kg did not result in any dostarlimab‐related effects on function of the CV system, respiratory system, or CNS”
✓ VerifiedFDA multi-discipline review, p. 39Source ↗
Genotox: Ames
Not conducted (biotechnology-derived product)
“No genetic toxicology or carcinogenicity studies were conducted or warranted to support this BLA submission, as dostarlimab‐gxly is a biotechnology‐derived pharmaceutical and the proposed indication is for advanced cancer.”
✓ VerifiedFDA multi-discipline review, p. 37Source ↗
Genotox: in vitro mammalian
Not conducted (biotechnology-derived product)
“No genetic toxicology or carcinogenicity studies were conducted or warranted to support this BLA submission, as dostarlimab‐gxly is a biotechnology‐derived pharmaceutical and the proposed indication is for advanced cancer.”
✓ VerifiedFDA multi-discipline review, p. 37Source ↗
Genotox: in vivo
Not conducted (biotechnology-derived product)
“No genetic toxicology or carcinogenicity studies were conducted or warranted to support this BLA submission, as dostarlimab‐gxly is a biotechnology‐derived pharmaceutical and the proposed indication is for advanced cancer.”
✓ VerifiedFDA multi-discipline review, p. 37Source ↗
Carcinogenicity model
Not conducted (ICH S6; advanced cancer per ICH S9)
“No studies have been performed to assess the potential of dostarlimab for carcinogenicity or genotoxicity which was considered acceptable based on ICH S6 (R1).”
Not required (biotechnology product for advanced cancer)
“No genetic toxicology or carcinogenicity studies were conducted or warranted to support this BLA submission, as dostarlimab‐gxly is a biotechnology‐derived pharmaceutical and the proposed indication is for advanced cancer.”
✓ VerifiedFDA multi-discipline review, p. 37Source ↗
hERG / QT
No hERG assay; no dostarlimab effects on monkey cardiovascular, respiratory or CNS function up to 100 mg/kg
“The administration of dostarlimab by a weekly IV dose for 4 weeks (5 total doses) to cynomolgus monkeys at dose levels of 0, 10, 30, or 100 mg/kg did not result in any dostarlimab‐related effects on function of the CV system, respiratory system, or CNS”
✓ VerifiedFDA multi-discipline review, p. 39Source ↗