TheraRadar

Pharma Intelligence, Simplified

Data updated: Mar 10, 2026

MYQORZO

AFICAMTEN
Cardiovascular Approved 2025-12-19
1
Indication
--
Phase 3 Trials
0
Years on Market

Details

Status
Prescription
First Approved
2025-12-19
Routes
ORAL
Dosage Forms
TABLET

Companies

Active Ingredient: AFICAMTEN

MYQORZO Approval History

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What MYQORZO Treats

1 indications

MYQORZO is approved for 1 conditions since its original approval in 2025. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Obstructive Hypertrophic Cardiomyopathy
Source: FDA Label

MYQORZO Boxed Warning

RISK OF HEART FAILURE MYQORZO reduces left ventricular ejection fraction (LVEF) and can cause heart failure due to systolic dysfunction [see Warnings and Precautions (5.1) ]. Echocardiogram assessments are required prior to and during treatment with MYQORZO to monitor for systolic dysfunction. Initiation of MYQORZO in patients with LVEF <55% is not recommended. Decrease the dose of MYQORZO if LVEF is <50% and ≥40% [see Dosage and Administration (2.2) and Warnings and Precautions (5.1) ] . Interr...

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Active Pipeline

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Ongoing clinical trials by development phase

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Key Completed Trials

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Completed studies with published results, ranked by significance

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Trial Timeline

Full development history with FDA approval milestones

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Understanding FDA Approval Types
Count Type What it means
- ORIG Original approval - drug first enters market
- SUPPL - Efficacy New indication (new disease/condition approved)
- SUPPL - Labeling Label text changes (warnings, dosing updates)
- SUPPL - Manufacturing Production changes (new facility)
- SUPPL - Chemistry Formulation changes (new dosage strength)

Green lines in the timeline show ORIG and Efficacy approvals - the clinically meaningful milestones.

MYQORZO FDA Label Details

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Indications & Usage

FDA Label (PDF)

MYQORZO is indicated for the treatment of adults with symptomatic obstructive hypertrophic cardiomyopathy (oHCM) to improve functional capacity and symptoms. MYQORZO is a cardiac myosin inhibitor indicated for the treatment of adults with symptomatic obstructive hypertrophic cardiomyopathy (oHCM) to improve functional capacity and symptoms.

⚠️ BOXED WARNING

WARNING: RISK OF HEART FAILURE MYQORZO reduces left ventricular ejection fraction (LVEF) and can cause heart failure due to systolic dysfunction [see Warnings and Precautions (5.1) ]. Echocardiogram assessments are required prior to and during treatment with MYQORZO to monitor for systolic dysfuncti...

MYQORZO Patents & Exclusivity

Latest Patent: Jul 2042
Exclusivity: Dec 2030

Patents (32 active)

US12370179 Expires Jul 15, 2042
US10836755 Expires Jan 18, 2039
+ 22 more patents

Exclusivity

NCE Until Dec 2030
NCE Until Dec 2030
NCE Until Dec 2030
NCE Until Dec 2030
NCE Until Dec 2030
Source: FDA Orange Book

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Data Sources

Data sourced from official FDA and NIH databases. Click links to verify on original sources.