Negative in Ames, in vitro CHO cytogenetic and in vivo mouse bone marrow micronucleus assays
“Tivozanib was not mutagenic in a bacterial reverse mutation (Ames) assay and was not clastogenic in an in vitro cytogenetic assay in Chinese hamster ovary cells or in an in vivo mouse bone marrow micronucleus assay.”
Not conducted (advanced cancer indication, ICH S9)
“As it is intended for advanced Renal Cell Carcinoma, in accordance with ICH S9 Nonclinical Evaluation for Anticancer Pharmaceuticals, carcinogenicity studies are not required.”
Rat fertility: increased epididymis/testis weights at ≥0.03 mg/kg/day; reduced mating and infertility at ≥0.3 mg/kg/day
“In animal studies assessing mating and fertility parameters, oral doses ≥ 0.03 mg/kg/day (0.2 times the maximum recommended clinical dose on a mg/m 2 basis) in rats were associated with increased epididymis and testis weights, and doses ≥ 0.3 mg/kg/day (2 times the maximum recommended clinical dose on a mg/m 2 basis) reduced mating and produced infertility.”
Telemetered monkeys: increased blood pressure at 3 mg/kg; no effects on heart rate, QT/QTc or QRS
“A dose of 3 mg/kg resulted in increases in systolic, diastolic and mean arterial blood pressure 90 minutes post-dose. There were no test article-related effects on heart rates, RR, PR, QT, QTcF, QTcQ intervals and the QRS duration at any dose level.”
✓ VerifiedFDA multi-discipline review, p. 150Source ↗
Not genotoxic overall: Ames negative; in vitro chromosome aberration positive without (not with) metabolic activation; rat micronucleus and comet negative