Drug Interactions between futibatinib and Scemblix
This report displays the potential drug interactions for the following 2 drugs:
- futibatinib
- Scemblix (asciminib)
Interactions between your drugs
asciminib futibatinib
Applies to: Scemblix (asciminib) and futibatinib
MONITOR: Coadministration with inhibitors of CYP450 3A4 that can also inhibit P-glycoprotein (P-gp) may increase the plasma concentrations of futibatinib. Futibatinib is a substrate of both the CYP450 3A4 isoenzyme and P-gp efflux transporter. Drug interaction studies have shown that single dose administration of futibatinib with multiple doses of itraconazole, a combined potent P-gp and CYP450 3A4 inhibitor, increased futibatinib peak plasma concentration (Cmax) and systemic exposure (AUC) by 51% and 41%, respectively, compared to futibatinib alone. Increased exposure to futibatinib may increase the risk and severity of adverse effects such as retinal pigment epithelial detachment, dry eye/corneal keratitis, pyrexia, hyperphosphatemia and soft tissue mineralization, palmar-plantar erythrodysesthesia syndrome, fatigue, nail toxicity, urinary tract infection, constipation, diarrhea, dry mouth, increased liver function tests (ALT and AST), stomatitis, abdominal pain, ascites, bile duct obstruction, and musculoskeletal pain. The interaction has not been studied with other, less potent dual inhibitors of CYP450 3A4 and P-gp.
MANAGEMENT: Caution is advised when futibatinib is used with inhibitors of CYP450 3A4 that can also inhibit P-gp. Clinical and laboratory monitoring for the development of adverse effects is recommended and the futibatinib dosage adjusted as necessary.
References (1)
- (2022) "Product Information. Lytgobi (futibatinib)." Taiho Oncology, Inc., 1
Drug and food interactions
futibatinib food
Applies to: futibatinib
GENERALLY AVOID: Grapefruit juice may increase the plasma concentrations of futibatinib. The proposed mechanism is inhibition of CYP450 3A4-mediated first-pass metabolism in the gut wall by certain compounds present in grapefruit. In general, the effect of grapefruit juice is concentration-, dose- and preparation-dependent, and can vary widely among brands. Certain preparations of grapefruit juice (e.g., high dose, double strength) have sometimes demonstrated potent inhibition of CYP450 3A4, while other preparations (e.g., low dose, single strength) have typically demonstrated moderate inhibition. Increased exposure to futibatinib may increase the risk of adverse effects such as retinal pigment epithelial detachment, dry eye/corneal keratitis, pyrexia, hyperphosphatemia and soft tissue mineralization, palmar-plantar erythrodysesthesia syndrome, fatigue, nail toxicity, urinary tract infection, constipation, diarrhea, dry mouth, increased liver function tests (ALT and AST), stomatitis, abdominal pain, ascites, bile duct obstruction, and musculoskeletal pain.
MANAGEMENT: Patients should be advised to avoid consumption of grapefruit or grapefruit juice during treatment with futibatinib.
References (1)
- (2022) "Product Information. Lytgobi (futibatinib)." Taiho Oncology, Inc., 1
asciminib food
Applies to: Scemblix (asciminib)
ADJUST DOSING INTERVAL: Food may reduce the oral bioavailability of asciminib. When a single 40 mg dose of asciminib was administered with a low-fat meal (400 calories; 25% fat) in healthy volunteers, asciminib peak plasma concentration (Cmax) and systemic exposure (AUC) decreased by 35% and 30%, respectively, compared to asciminib administered in the fasted state. Administration with a high-fat meal (1000 calories; 50% fat) decreased the Cmax and AUC of asciminib by 68% and 62%, respectively.
MANAGEMENT: To ensure adequate asciminib exposures, food consumption should be avoided for at least 2 hours before and 1 hour after taking asciminib.
References (2)
- (2021) "Product Information. Scemblix (asciminib)." Novartis Pharmaceuticals
- (2022) "Product Information. Scemblix (asciminib)." Novartis Pharmaceuticals UK Ltd, Scemblix 20 mg film-
Therapeutic duplication warnings
No warnings were found for your selected drugs.
Therapeutic duplication warnings are only returned when drugs within the same group exceed the recommended therapeutic duplication maximum.
See also
Drug Interaction Classification
Highly clinically significant. Avoid combinations; the risk of the interaction outweighs the benefit. | |
Moderately clinically significant. Usually avoid combinations; use it only under special circumstances. | |
Minimally clinically significant. Minimize risk; assess risk and consider an alternative drug, take steps to circumvent the interaction risk and/or institute a monitoring plan. | |
No interaction information available. |
Further information
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