Cytokinetics (CYTK) said Thursday that the United Kingdom's Medicines and Healthcare products Regulatory Agency has granted aficamten marketing authorisation across the UK for the treatment of symptomatic obstructive hypertrophic cardiomyopathy.
Guidance from the National Institute for Health and Care Excellence states that aficamten can be used to treat symptomatic obstructive hypertrophic cardiomyopathy in eligible adults with NYHA class II to III, in England and Wales, the company said.
Aficamten can only be used as an add-on to individually optimised standard care including beta-blockers, non-dihydropyridine calcium-channel blockers or disopyramide, or alone if these treatments are contraindicated, Cytokinetics said.
The company said that the MHRA's assessment was based on data from its phase 3 SEQUOIA-HCM study in 282 adults.
Shares of the company were up 2.2% in Thursday trading.
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