Trelegy Ellipta once-daily single inhaler triple therapy gains marketing authorisation in Europe for the treatment of COPD

GSK

16 November 2017 - GlaxoSmithKline and Innoviva today announced that the European Commission has granted marketing authorisation for Trelegy Ellipta (fluticasone furoate/umeclidinium/vilanterol) as a maintenance treatment in adult patients with moderate to severe chronic obstructive pulmonary disease who are not adequately treated by a combination of an inhaled corticosteroid and a long-acting beta2-agonist.

Trelegy Ellipta is the first once-daily single inhaler triple therapy to be approved in Europe. It is a combination of an inhaled corticosteroid, a long-acting muscarinic antagonist and a long-acting beta 2-adrenergic agonist, delivered once daily in GSK’s Ellipta dry powder inhaler.

The first European launch is expected to take place before the end of the year.

Read GSK press release

Michael Wonder

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Michael Wonder