Combination of | |
---|---|
Fluticasone furoate | Corticosteroid |
Vilanterol | Ultra-long-acting β2 agonist |
Clinical data | |
Trade names | Breo Ellipta, Relvar Ellipta |
AHFS/Drugs.com | breo-ellipta |
License data | |
Routes of administration | Inhalation (DPI) |
ATC code | |
Legal status | |
Legal status | |
Identifiers | |
KEGG |
Fluticasone furoate/vilanterol (FF/VI), sold under the brand name Breo Ellipta among others, is a combination medication for the treatment of chronic obstructive pulmonary disease (COPD) and asthma.[2] It contains fluticasone furoate, an inhaled corticosteroid, and vilanterol, an ultra-long-acting β2 agonist (ultra-LABA).[2]
In 2013, the drug was approved for use in the United States by the Food and Drug Administration (FDA) for long-term maintenance treatment of airflow obstruction in people with COPD, including chronic bronchitis and emphysema,[4] and the European Medicines Agency approved it as a second-line therapy for the treatment of COPD and asthma.[5] There were, however, concerns that LABAs such as vilanterol increase the risk of deaths due to asthma. In 2017, the FDA states that they were not justified.[4]
It is on the World Health Organization's List of Essential Medicines.[6] In 2020, it was the 115th most commonly prescribed medication in the United States, with more than 5 million prescriptions.[7][8]
This drug was approved by the FDA for use as a long-term, once-daily, maintenance treatment in people with COPD in 2013. Labeling changed on 30 April 2015, to add an indication for a once-daily treatment of asthma in people 18 years or older.[2] The exclusivity for a new product ended in May 2016, in the United States, and the exclusivity on the indication for asthma expired on 30 April 2018.[9] The patent for both indications expires on 3 August 2021.[9] The European Medicines Agency approved the drug for marketing on 13 November 2013.[10]
GlaxoSmithKline manufactures this drug. As of 31 December 2015, FF/VI inhalation powder was approved for marketing in 73 countries, and had been launched in 45 countries.[11] Within the trade name, the "Ellipta" is the dry powder inhaler that the medication is administered in. Innoviva developed the active substance vilanterol, and receives royalties on sales.[12]
There is tentative evidence as of 2016 that it is better than placebo for asthma.[13] Evidence is less strong in children.[13]