Wednesday, July 8, 2026

Drug profile · INN

mavacamten

mavacamten (CAMZYOS) is a cardiac myosin inhibitor. Associated with Bristol-Myers Squibb Australia Pty Ltd. Route of administration: oral. Current US regulatory status: approved.

FDA: approved EMA: approved TGA: approved PMDA: approved Cardiovascular system (C01) C01EB
US status approved
Patents linked 0
Pipeline programs 1
News articles 0
Drug details — mavacamten
US status
approved
Class
Cardiovascular system (C01)
Route
ORAL
Patents
0
Programs
1
Data quality
0.84

Quick answer

mavacamten (CAMZYOS) is a cardiac myosin inhibitor. Associated with Bristol-Myers Squibb Australia Pty Ltd. Route of administration: oral. Current US regulatory status: approved.

Key facts

INN mavacamten
Brand CAMZYOS
Mechanism Cardiac myosin inhibitor
Target Cardiac myosin
Therapeutic class Cardiovascular system (C01)
Route ORAL
Formulation CAPSULE
ATC code C01EB

Mechanism of action

Cardiac myosin inhibitor

Primary target: Cardiac myosin

Approval history

Authority Status Date
FDA approved
EMA approved
TGA approved
PMDA approved

Pipeline programs

  1. CV027-010 Phase 3 · Bristol-Myers Squibb Australia · Symptomatic Obstructive Hypertrophic Cardiomyopathy

Related & competitor drugs

  1. alirocumab Cardiovascular system (C10)
  2. aliskiren Cardiovascular system (C09)
  3. azilsartan medoxomil Cardiovascular system (C09)
  4. bempedoic acid Cardiovascular system (C10)
  5. bosentan Cardiovascular system (C02)
  6. dofetilide Cardiovascular system (C01)

Frequently asked questions

What is mavacamten?

mavacamten (CAMZYOS) is a cardiac myosin inhibitor. Associated with Bristol-Myers Squibb Australia Pty Ltd. Route of administration: oral. Current US regulatory status: approved.

What is the brand name for mavacamten?

CAMZYOS is a marketed brand name for mavacamten. Check FDA Drugs@FDA for the current US label holder and prescribing information.

What is the US approval status of mavacamten?

mavacamten has approved status in the United States according to our Drugs@FDA-derived records. Verify on the official FDA label before clinical or commercial decisions.