“In accordance with ICH S6, the Applicant did not submit genotoxicity studies; routine tests for genotoxicity are not applicable to biotherapeutics”
✓ VerifiedFDA pharmacology/toxicology review, p. 75Source ↗
Carcinogenicity
Not conducted (advanced cancer, ICH S9)
“In accordance with ICH S9 the Applicant did not conduct carcinogenicity studies with ramucirumab because these studies are not warranted to support marketing for therapeutics intended to treat patients with advanced cancer.”
✓ VerifiedFDA pharmacology/toxicology review, p. 75Source ↗
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-based assessment of VEGFR2 inhibition in pregnancy
“Dedicated reproductive toxicology studies examining the effects of ramucirumab administration to animals during pregnancy have not been conducted. Instead the Applicant submitted a literature based assessment of the potential effects of inhibition of VEGFR2 signaling during pregnancy.”
✓ VerifiedFDA pharmacology/toxicology review, p. 20Source ↗
Safety pharmacology
Incorporated into 5- and 39-week monkey studies; no effects on blood pressure, ECG or body temperature
“No dedicated safety pharmacology studies have been performed with ramucirumab but safety pharmacology parameters were assessed as part of the GLP-compliant 5-and 39-week toxicology studies in Cynomolgus monkeys.”
“In accordance with ICH S6, the Applicant did not submit genotoxicity studies; routine tests for genotoxicity are not applicable to biotherapeutics as it is not expected that monoclonal antibodies will react with DNA or other chromosomal material.”
✓ VerifiedFDA pharmacology/toxicology review, p. 75Source ↗
Genotox: in vitro mammalian
Not conducted (ICH S6)
“In accordance with ICH S6, the Applicant did not submit genotoxicity studies; routine tests for genotoxicity are not applicable to biotherapeutics as it is not expected that monoclonal antibodies will react with DNA or other chromosomal material.”
✓ VerifiedFDA pharmacology/toxicology review, p. 75Source ↗
Genotox: in vivo
Not conducted (ICH S6)
“In accordance with ICH S6, the Applicant did not submit genotoxicity studies; routine tests for genotoxicity are not applicable to biotherapeutics as it is not expected that monoclonal antibodies will react with DNA or other chromosomal material.”
✓ VerifiedFDA pharmacology/toxicology review, p. 75Source ↗
Carcinogenicity model
Not conducted: not warranted for therapeutics for advanced cancer (ICH S9)
“In accordance with ICH S9 the Applicant did not conduct carcinogenicity studies with ramucirumab because these studies are not warranted to support marketing for therapeutics intended to treat patients with advanced cancer.”
✓ VerifiedFDA pharmacology/toxicology review, p. 75Source ↗
Carcinogenicity timing
Not required for an advanced-cancer product
“Carcinogenicity studies were not required to support the licensing application for a product to treat advanced human cancer”
✓ VerifiedFDA pharmacology/toxicology review, p. 10Source ↗
hERG / QT
No hERG or stand-alone safety pharmacology; no ECG or blood pressure changes in monkey toxicity studies
“There were no ramucirumab-related changes in ECG measurements or in blood pressure in either study, though hypertension is a clinical finding associated with ramucirumab treatment.”
✓ VerifiedFDA pharmacology/toxicology review, p. 19Source ↗