Concomitant use may decrease vorasidenib plasma concentrations and reduce anti-tumor activity.
Source: NLP:vorasidenib
Brand names: Voranigo
Isocitrate Dehydrogenase 1 Inhibitor · Isocitrate Dehydrogenase 2 Inhibitor · Isocitrate Dehydrogenase 1 Inhibitors · Isocitrate Dehydrogenase 2 Inhibitors · Cytochrome P450 3A Inducers
Route: Oral
Contraindications
4 CONTRAINDICATIONS None. None. ( 4 )
Pregnancy & Breastfeeding
8.1 Pregnancy Risk Summary Based on findings from animal studies and its mechanism of action [see Clinical Pharmacology (12.1) ] , VORANIGO can cause fetal harm when administered to a pregnant woman. There are no available data on VORANIGO use in pregnant women to inform a drug-associated risk. In animal embryo-fetal development studies, oral administration of vorasidenib to pregnant rats and rabbits during the period of organogenesis caused embryo-fetal toxicity at ≥8 times the human exposure based on the AUC at the highest recommended dose (see Data ) . Advise pregnant women of the potential risk to the fetus. In the U.S. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2% to 4% and 15% to 20%, respectively. Data Animal Data In an embryo-fetal development study, vorasidenib was administered to pregnant rats via oral gavage at dose levels of 10, 25, and 75 mg/kg/day during the period of organogenesis (gestation days 6 to 17). Embryo-fetal toxicity (higher incidence of early resorptions, and visceral malformations of kidney and testes) occurred in rats at the maternally toxic dose of 75 mg/kg/day (approximately 170 times the human exposure based on the AUC at the highest recommended dose). Malformation of heart occurred in a rat at a dose of 25 mg/kg (approximately 97 times the human exposure based on the AUC at the highest recommended dose). Dose-related delayed ossification of bones and short ribs associated with decreased fetal body weights was observed at 10 and 25 mg/kg/day in the absence of maternal toxicity and at 75 mg/kg/day. The dose of 10 mg/kg/day is ≥45 times the human exposure based on the AUC at the highest recommended dose. In an embryo-fetal development study, oral administration of vorasidenib to pregnant rabbits at dose levels of 2, 6, and 18 mg/kg/day during the period of organogenesis (gestation days 6 to 19) resulted in maternal toxicity at all doses (≥1.5 times the
4 interactions on record
Concomitant use may decrease vorasidenib plasma concentrations and reduce anti-tumor activity.
Source: NLP:vorasidenib
Concomitant use may increase vorasidenib plasma concentrations and increase risk of adverse reactions.
Source: NLP:vorasidenib
Concomitant use may decrease hormonal contraceptive concentrations, leading to contraception failure and breakthrough bleeding.
Source: NLP:vorasidenib
Smoking tobacco with moderate CYP1A2 inducers may decrease vorasidenib plasma concentrations and reduce anti-tumor activity.
Source: NLP:vorasidenib