
Camzoy2.5 mg
Beacon Pharmaceuticals PLC
Established / FDA-Approved Indication Mavacamten is indicated for the treatment of adults with symptomatic New York Heart Association (NYHA) class II-III obstructive hypertrophic cardiomyopathy…
Efficacy of Mavacamten in this population is based on randomized, double-blind, placebo-controlled trials (e.g. EXPLORER-HCM) demonstrating improvement in peak oxygen uptake, post-exercise left ventricular outflow tract (LVOT) gradient, NYHA functional class, and patient-reported symptom burden.
Mavacamten is not indicated for non-obstructive HCM, for HCM in children, or for other forms of heart failure. It is a first-in-class, highly specialised agent intended only for use within a restricted access program by physicians experienced in the management of HCM; it is not a general-practice medication.
| Step | Dose | Notes |
|---|---|---|
| Starting dose | 5 mg orally once daily | Confirm LVEF ≥55% and absence of pregnancy before starting |
| Available strengths | 2.5 mg, 5 mg, 10 mg, 15 mg capsules | Dose is individually titrated |
| Titration | Adjusted at scheduled visits (approx. every 4 weeks initially, then every 12 weeks) | Based on echocardiographic LVEF and Valsalva LVOT gradient, and symptoms |
| Maximum dose | 15 mg once daily | Do not exceed without specialist guidance |
Not established; Mavacamten is not approved for use in children (see Use in Special Populations).
No dose adjustment is required for mild-to-moderate renal impairment. Data in severe renal impairment are limited; use with caution.
A lower starting dose and slower titration are recommended in moderate hepatic impairment; Mavacamten has not been studied in severe hepatic impairment and is not recommended.
Take Mavacamten exactly as prescribed by a cardiology specialist, at the same time each day, on an empty stomach (at least 2 hours before or 2 hours after a meal), because food increases absorption. Do not stop, skip doses, share this medicine, or change the dose without direct instruction from the prescribing physician, since abrupt changes can affect heart function.
Report any new or worsening shortness of breath, swelling of the legs/ankles, fatigue, dizziness, or fainting to the prescribing physician immediately.
Mavacamten should not be initiated in patients with a left ventricular ejection fraction (LVEF) below 55% (see Precautions and Warnings).
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