Drug Interactions between Caplyta and lapatinib
This report displays the potential drug interactions for the following 2 drugs:
- Caplyta (lumateperone)
- lapatinib
Interactions between your drugs
lapatinib lumateperone
Applies to: lapatinib and Caplyta (lumateperone)
MONITOR: Coadministration with inhibitors of CYP450 3A4 may increase the plasma concentrations of lumateperone. In vitro studies show that multiple enzymes are involved in the metabolism of lumateperone, including but not limited to uridine 5'-diphospho-glucuronosyltransferases (UGT) 1A1, 1A4, and 2B15; aldoketoreductase (AKR) 1C1, 1B10, and 1C4; and cytochrome P450 (CYP450) 3A4, 2C8, and 1A2. When coadministered with itraconazole, a potent CYP450 3A4 inhibitor, lumateperone peak plasma concentration (Cmax) and systemic exposure (AUC) increased by approximately 3.5- and 4-fold, respectively. When coadministered with diltiazem, a moderate CYP450 3A4 inhibitor, lumateperone Cmax and AUC increased by approximately 2- and 2.5-fold, respectively. No data are available for other, less potent CYP450 3A4 inhibitors.
MANAGEMENT: Caution is advised when lumateperone is used with CYP450 3A4 inhibitors. Patients should be monitored for increased adverse effects such as extrapyramidal symptoms, tardive dyskinesia, hyperglycemia, dyslipidemia, hyperprolactinemia, neutropenia, leukopenia, orthostatic hypotension, syncope, seizures, cognitive and motor impairment, dysphagia, and heat-related illnesses due to disruption of body temperature regulation.
References (2)
- (2020) "Product Information. Caplyta (lumateperone)." Intra-Cellular Therapies, Inc.
- (2022) "Product Information. Caplyta (lumateperone)." Intra-Cellular Therapies, Inc., SUPPL-9
Drug and food interactions
lapatinib food
Applies to: lapatinib
GENERALLY AVOID: Grapefruit juice may increase the plasma concentrations of lapatinib. The proposed mechanism is inhibition of CYP450 3A4-mediated first-pass metabolism in the gut wall by certain compounds present in grapefruits.
ADJUST DOSING INTERVAL: Food can significantly increase the oral bioavailability of lapatinib. According to the manufacturer, lapatinib peak plasma concentration (Cmax) was approximately 2.5- and 3-fold higher and systemic exposure (AUC) 3- and 4-fold higher when administered with a low fat meal (5% fat; 500 calories) or with a high-fat meal (50% fat; 1000 calories), respectively, compared to fasting. Dividing the daily dose also resulted in an approximately 2-fold higher systemic exposure at steady state compared to the same total dose administered once daily.
MANAGEMENT: Patients treated with lapatinib should preferably avoid the consumption of grapefruit or grapefruit juice. The manufacturer recommends that lapatinib be administered at least one hour before or one hour after a meal. The lapatinib dose is administered once daily and should not be divided.
References (1)
- (2007) "Product Information. Tykerb (lapatinib)." Novartis Pharmaceuticals
lumateperone food
Applies to: Caplyta (lumateperone)
GENERALLY AVOID: Grapefruit and grapefruit juice may increase the plasma concentrations of lumateperone. The proposed mechanism is inhibition of CYP450 3A4-mediated first-pass metabolism in the gut wall by certain compounds present in grapefruit. Inhibition of hepatic CYP450 3A4 may also contribute. The interaction has not been studied with grapefruit but has been reported for other CYP450 3A4 inhibitors. In a drug interaction study, the strong CYP450 3A4 inhibitor itraconazole increased lumateperone peak plasma concentration (Cmax) and systemic exposure (AUC) approximately 3.5- and 4-fold, respectively, while diltiazem (a moderate CYP450 3A4 inhibitor) increased lumateperone Cmax and AUC approximately 2- and 2.5-fold, respectively. 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.
When administered with a high-fat meal, lumateperone Cmax decreased by 33% while its AUC increased by 9% and its median time to peak plasma concentration (Tmax) was delayed by about 1 hour.
MANAGEMENT: Lumateperone should be administered with food. Coadministration of grapefruit or grapefruit juice with lumateperone should be avoided.
References (1)
- (2020) "Product Information. Caplyta (lumateperone)." Intra-Cellular Therapies, Inc.
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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