Negative in Ames, mouse lymphoma and rat bone marrow micronucleus assays
“CBM was negative for genotoxicity in in vitro (Ames, mouse lymphoma) and in vivo (rat bone marrow micronucleus) assays.”
✓ VerifiedFDA pharmacology/toxicology review, p. 8Source ↗
Carcinogenicity
26-week rasH2 mouse and 2-year rat: no drug-related neoplasms
“A 26-week study in transgenic RasH2 mice and a 2-year study in Sprague-Dawley rats were conducted. The executive carcinogenicity assessment committee concluded that the studies were adequate and that there were no drug-related neoplasms in either study.”
✓ VerifiedFDA pharmacology/toxicology review, p. 2Source ↗
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
Rat EFD: embryofetal death, lower fetal weight and incomplete ossification at maternally toxic high dose
“Oral administration of CBM to pregnant rats throughout organogenesis at doses of up to 60 mg/kg/day resulted in increased embryofetal mortality, reduced fetal body weights, and incomplete fetal skeletal ossification at the highest dose tested, which was associated with maternal toxicity.”
✓ VerifiedFDA pharmacology/toxicology review, p. 9Source ↗
“CBM produced concentration-dependent inhibition of hERG-mediated potassium currents; the IC50 was estimated as 1869 μM, which is 11X higher than the clinical steady state Cmax after daily dosing at the MRHD of 400 mg (45.5 μg/mL; 169 μM).”
✓ VerifiedFDA pharmacology/toxicology review, p. 6Source ↗
Genotox: Ames
Negative
“CBM was negative for genotoxicity in in vitro (Ames, mouse lymphoma) and in vivo (rat bone marrow micronucleus) assays.”
✓ VerifiedFDA pharmacology/toxicology review, p. 8Source ↗
Genotox: in vitro mammalian
Mouse lymphoma assay: negative
“CBM was negative for genotoxicity in in vitro (Ames, mouse lymphoma) and in vivo (rat bone marrow micronucleus) assays.”
✓ VerifiedFDA pharmacology/toxicology review, p. 8Source ↗
Genotox: in vivo
Rat bone marrow micronucleus: negative
“CBM was negative for genotoxicity in in vitro (Ames, mouse lymphoma) and in vivo (rat bone marrow micronucleus) assays.”
✓ VerifiedFDA pharmacology/toxicology review, p. 8Source ↗
Carcinogenicity model
26-week Tg rasH2 mouse (up to 35 mg/kg/day) and rat up to 90 weeks (up to 20 mg/kg): no tumor increase
“Administration of CBM to Tg.rasH2 mice at oral doses up to 35 mg/kg/day for 26 weeks did not result in an increase in tumors. Administration to rats for up to 90 weeks did not result in an increase in tumors at oral doses up to 20 mg/kg”
✓ VerifiedFDA pharmacology/toxicology review, p. 8Source ↗
Carcinogenicity timing
26-week rasH2 mouse and 2-year rat studies completed before the marketing application; judged adequate
“A 26-week study in transgenic RasH2 mice and a 2-year study in Sprague-Dawley rats were conducted. The executive carcinogenicity assessment committee concluded that the studies were adequate and that there were no drug-related neoplasms in either study.”
✓ VerifiedFDA pharmacology/toxicology review, p. 2Source ↗
“CBM produced concentration-dependent inhibition of hERG-mediated potassium currents; the IC50 was estimated as 1869 μM, which is 11X higher than the clinical steady state Cmax after daily dosing at the MRHD of 400 mg (45.5 μg/mL; 169 μM).”
✓ VerifiedFDA pharmacology/toxicology review, p. 6Source ↗
Not genotoxic overall: Ames negative; in vitro chromosome aberration positive without (not with) metabolic activation; rat micronucleus and comet negative