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Pharma & Biotech

GlaxoSmithKline gets 'positive opinion' from EMA panel for three-in-one inhaled COPD treatment

The once-a-day triple inhaler combines the drugs fluticasone furoate, umeclidinium and vilanterol and will have a proposed brand name of Trelegy Ellipta

GlaxoSmithKline plc (LON:GSK) has announced that a European Medicines Agency (EMA) panel has recommended a three-in-one inhaled drug developed with US firm Innoviva, Inc.(NASDAQ: INVA) as a treatment for severe chronic obstructive pulmonary disease (COPD).

The once-a-day triple inhaler combines the drugs fluticasone furoate, umeclidinium and vilanterol and will have a proposed brand name of Trelegy Ellipta.

READ: GSK asthma study results published in medical journal and presented at industry meeting

The treatment will be used for patients who are not adequately treated by a combination of an inhaled corticosteroid and a long-acting beta2-agonist.

Patrick Vallance, Glaxo's president of R&D, said, "We believe once-daily single inhaler triple therapy, if approved, would provide an important option for appropriate patients with COPD who are receiving ICS/LABA and require additional bronchodilation, avoiding the need for multiple inhalers."

In a statement, Glaxo said the EMA's Committee for Medicinal Products for Human Use (CHMP) had given a “positive opinion for the treatment”.

A CHMP positive opinion is one of the final steps before marketing authorisation from the European Commission. A final decision is expected around the end of 2017, the company said.

READ: GSK confirms plans to sell Horlicks in the UK and cut 320 jobs as it prioritises drugs business

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