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Mavacamten
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Trade names | Camzyos |
Other names | MYK-461 |
License data |
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Routes of administration |
By mouth |
Drug class | Cardiac myosin inhibitor |
ATC code | |
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Chemical and physical data | |
Formula | C15H19N3O2 |
Molar mass | 273.336 g·mol−1 |
3D model (JSmol) | |
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Mavacamten, sold under the brand name Camzyos, is a medication used to treat obstructive hypertrophic cardiomyopathy.
Mavacamten is a cardiac myosin inhibitor. It was developed by MyoKardia, a subsidiary of Bristol Myers Squibb.
Mavacamten was approved for medical use in the United States in April 2022. The US Food and Drug Administration (FDA) considers it to be a first-in-class medication.
Medical uses
Mavacamten is indicated for the treatment of adults with symptomatic New York Heart Association class II-III obstructive hypertrophic cardiomyopathy to improve functional capacity and symptoms.
History
Mavacamten was granted orphan drug designation by the U.S. Food and Drug Administration (FDA).
Society and culture
Legal status
On 26 April 2023, the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) adopted a positive opinion, recommending the granting of a marketing authorization for the medicinal product Camzyos, intended for the treatment of symptomatic obstructive hypertrophic cardiomyopathy (oHCM). The applicant for this medicinal product is Bristol-Myers Squibb Pharma EEIG.
Names
Mavacamten is the international nonproprietary name (INN).
Further reading
- Xie J, Wang Y, Xu Y, Fine JT, Lam J, Garrison LP (2022). "Assessing health-related quality-of-life in patients with symptomatic obstructive hypertrophic cardiomyopathy: EQ-5D-based utilities in the EXPLORER-HCM trial". Journal of Medical Economics. 25 (1): 51–58. doi:10.1080/13696998.2021.2011301. PMID 34907813.
External links
- Clinical trial number NCT03470545 for "Clinical Study to Evaluate Mavacamten (MYK-461) in Adults With Symptomatic Obstructive Hypertrophic Cardiomyopathy (EXPLORER-HCM)" at ClinicalTrials.gov