Indication
Know Medicine, Follow Guideline
Details coming soon
Details coming soon
| Clinical Information | Administration Information |
|---|---|
|
Indication: Obstructive Hypertrophic Cardiomyopathy Age: Adult Condition: New York Heart Association class II-III |
Dose: Oral – 5 mg Frequency: once daily Note: Starting dose. Initiation or up-titration in patients with left ventricular ejection fraction less than 55% not recommended. |
|
Indication: Obstructive Hypertrophic Cardiomyopathy Age: Adult Condition: New York Heart Association class II-III |
Dose: Oral – 2.5, 5, 10, or 15 mg Frequency: once daily Note: Allowable subsequent doses with titration. The maximum recommended dose is 15 mg once daily. Initiation or up-titration in patients with left ventricular ejection fraction less than 55% not recommended. |
| Clinical Information | Administration Information |
|---|---|
|
Age: Child |
Dose: Not applicable – No approved pediatric dosage available Note: No approved pediatric dosage available |
| Clinical Information | Administration Information |
|---|---|
|
Condition: Mild-to-moderate renal impairment (estimated glomerular filtration rate 30-89 mL/min/1.73 m2) |
Dose: Unknown Note: No dosage adjustment required |
|
Condition: Severe renal impairment and kidney failure, including patients on dialysis (estimated glomerular filtration rate less than 30 mL/min/1.73 m2) |
Dose: Unknown Note: Dosage adjustment unknown |
Administer mavacamten orally as a whole capsule once daily, with or without food, at approximately the same time each day. Do not break, open, or chew the capsules. The recommended starting dose is 5 mg, with subsequent titration to 2.5 mg, 5 mg, 10 mg, or 15 mg based on echocardiographic assessment of left ventricular ejection fraction (LVEF) and Valsalva LVOT gradient. Treatment initiation is not recommended in patients with LVEF less than 55%. Dose reduction or treatment interruption is required for patients initiating weak to moderate CYP2C19 inhibitors or moderate to strong CYP3A4 inhibitors, as well as those with intercurrent illness or LVEF reduction below 50%. Use in pediatric populations has not been established.
Details coming soon
Details coming soon
Details coming soon
Clinical & regulatory information on this page is compiled from the following government sources:
DISCLAIMER: This drug information content is provided for informational purposes only and is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Patients should always consult their physician with any questions regarding a medical condition and to obtain medical advice and treatment.