Drug Interactions between mavacamten and modafinil
This report displays the potential drug interactions for the following 2 drugs:
- mavacamten
- modafinil
Interactions between your drugs
modafinil mavacamten
Applies to: modafinil and mavacamten
GENERALLY AVOID: Coadministration with inhibitors of CYP450 2C19 that can also induce CYP450 3A4 may alter the plasma concentrations of mavacamten. According to the prescribing information, mavacamten is primarily metabolized by CYP450 2C19 (74%) and to a lesser extent by CYP450 3A4 (18%) and 2C9 (8%). In healthy CYP450 2C19 normal and rapid metabolizers, concomitant use of mavacamten (15 mg) with the weak CYP450 2C19 inhibitor omeprazole (20 mg) once daily increased mavacamten systemic exposure (AUC) by 48% but had no effect on peak plasma concentration (Cmax). Because mavacamten reduces systolic contraction and left ventricular ejection fraction, increased exposure may potentiate the risk of heart failure. By contrast, concomitant use of a single dose of mavacamten (15 mg) with the potent CYP450 2C19 and 3A4 inducer rifampin (600 mg once daily) is predicted to decrease mavacamten Cmax and AUC by 22% and 87%, respectively, in CYP450 2C19 normal metabolizers, and by 4% and 69%, respectively, in CYP450 2C19 poor metabolizers. The interaction has not been studied with drugs that can both inhibit CYP450 2C19 and induce CYP450 3A4.
MANAGEMENT: The prescribing information provides dosing recommendations for mavacamten when used with weak inhibitors of CYP450 2C19, but no guidance is available for concomitant use of CYP450 2C19 inhibitors that also induce CYP450 3A4. Until more data are available, it may be advisable to avoid prescribing mavacamten with these drugs when possible. Otherwise, close medical supervision and monitoring of left ventricular ejection fraction (LVEF) are recommended. New or worsening arrhythmia, dyspnea, chest pain, fatigue, palpitations, leg edema, or elevations in N-terminal pro-B-type natriuretic peptide (NT-proBNP) may be signs and symptoms of heart failure and should also prompt an echocardiographic evaluation of cardiac function. Asymptomatic LVEF reduction, intercurrent illnesses (e.g., serious infections), and arrhythmias (e.g., atrial fibrillation or other uncontrolled tachyarrhythmia) require additional dosing considerations.
References (2)
- (2022) "Product Information. Camzyos (mavacamten)." MyoKardia Inc
- (2023) "Product Information. Camzyos (mavacamten)." (Obsolete) Bristol-Myers Squibb Australia Pty Ltd, 2
Drug and food interactions
mavacamten food
Applies to: mavacamten
GENERALLY AVOID: Grapefruit juice may increase the plasma concentrations of mavacamten. 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 juice, but has been reported for other CYP450 3A4 inhibitors. According to the prescribing information, mavacamten is primarily metabolized by CYP450 2C19 (74%) and to a lesser extent by CYP450 3A4 (18%) and 2C9 (8%). When mavacamten (25 mg) was coadministered with the moderate CYP450 3A4 inhibitor verapamil (sustained-release 240 mg) in intermediate and normal metabolizers of CYP450 2C19, mavacamten systemic exposure (AUC) increased by 15% and peak plasma concentration (Cmax) increased by 52%. Concomitant use of mavacamten with diltiazem, another moderate CYP450 3A4 inhibitor, in CYP450 2C19 poor metabolizers is predicted to increase mavacamten AUC and Cmax by up to 55% and 42%, respectively. Concomitant use of mavacamten (15 mg) with the potent CYP450 3A4 inhibitor ketoconazole (400 mg once daily) is predicted to increase mavacamten AUC and Cmax by up to 130% and 90%, respectively. Because mavacamten reduces systolic contraction and left ventricular ejection fraction, increased exposure may potentiate the risk of heart failure. 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.
Food does not affect the extent of absorption of mavacamten. No clinically significant difference in mavacamten exposure was observed following administration with a high-fat meal. However, the time to reach peak plasma concentration (Tmax) was increased by 4 hours.
MANAGEMENT: Mavacamten may be administered with or without food. Patients should avoid consumption of grapefruit and grapefruit juice during treatment with mavacamten.
References (2)
- (2022) "Product Information. Camzyos (mavacamten)." MyoKardia Inc
- (2023) "Product Information. Camzyos (mavacamten)." (Obsolete) Bristol-Myers Squibb Australia Pty Ltd, 2
modafinil food
Applies to: modafinil
Administration with food may delay the absorption of modafinil (the racemate) and armodafinil (the R-enantiomer) without significantly affecting their overall bioavailability. According to the product labeling, modafinil's absorption may be delayed by approximately one hour if taken with food. Similarly, the time to reach peak plasma concentration (Tmax) of armodafinil may be delayed by approximately 2 to 4 hours in the fed state.
References (2)
- (2001) "Product Information. Provigil (modafinil)." Cephalon, Inc
- (2007) "Product Information. Nuvigil (armodafinil)." Cephalon 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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