Negative in Ames, in vitro human lymphocyte cytogenetic and in vivo rat micronucleus assays
“Selinexor was not mutagenic in vitro in a bacterial reverse mutation (Ames) assay and was not clastogenic in both the in vitro cytogenetic assay in human lymphocytes or in the in vivo rat micronucleus assay.”
✓ VerifiedFDA multi-discipline review, p. 30Source ↗
Carcinogenicity
Not conducted
“Carcinogenicity studies were not conducted to support the use of selinexor for the proposed indication.”
✓ VerifiedFDA multi-discipline review, p. 30Source ↗
Reproductive & developmental
Rat EFD: reduced fetal weight and delayed or incomplete ossification at >=0.75 mg/kg/day
“Adverse developmental outcomes occurred at ≥ 0.75 mg/kg/day and included alterations to growth (e.g., fetal weights in the 0.75 and 2 mg/kg/day groups were 13.5% and 32.4% lower than controls) and structural abnormalities (such as incomplete or delayed ossification of sternebra(e) and/or vertebral arches, and/or unossified and bent ribs).”
✓ VerifiedFDA multi-discipline review, p. 30Source ↗
Safety pharmacology
hERG IC50 20.6 μM (HEK293 patch clamp)
“Selinexor was evaluated for its ability to inhibit the hERG channel (IC50 = 20.6 μM) using whole cell patch clamp in stably-transfected HEK293 cells (Study: KS-0055).”
✓ VerifiedFDA multi-discipline review, p. 33Source ↗
Not genotoxic overall: Ames negative; in vitro chromosome aberration positive without (not with) metabolic activation; rat micronucleus and comet negative