Negative in Ames, in vitro micronucleus and in vivo rat micronucleus assays
“Revumenib was tested in GLP in vitro bacterial reverse mutation and mammalian cell micronucleus assays and an in vivo micronucleus assay in Sprague Dawley rats. There were no revumenib-related genotoxic effects in vitro or in vivo.”
✓ VerifiedFDA multi-discipline review, p. 75Source ↗
Carcinogenicity
Not conducted (not warranted for advanced cancer indication)
“Carcinogenicity studies were not warranted for the proposed indication.”
✓ VerifiedFDA multi-discipline review, p. 76Source ↗
Reproductive & developmental
Rat EFD: resorptions, post-implantation loss and malformations at all doses (0.6x human AUC)
“There was a dose-dependent increase in the number of resorptions (including total litter resorption at 300 mg/kg/day), post-implantation loss, and malformations at all revumenib doses, suggesting potential fetal toxicity at exposures 0.6 times the human exposure (AUC) at the recommended dose of 270 mg twice daily.”
✓ VerifiedFDA multi-discipline review, p. 34Source ↗
Safety pharmacology
Revumenib and metabolite M1 inhibit hERG (IC50 4.75 and 3.46 µM); QTc prolongation and premature atrial contractions in dogs
“The IC50 values for hERG inhibition were 4.75 and 3.46 µM for revumenib and M1, respectively, and suggest that M1 contributes to the effects of hERG inhibition. Increased QTc interval duration and premature atrial contractions were seen after repeated dosing with 225 mg/kg/day in dogs.”
✓ VerifiedFDA multi-discipline review, p. 32Source ↗
Not genotoxic overall: Ames negative; in vitro chromosome aberration positive without (not with) metabolic activation; rat micronucleus and comet negative