Glaxo/Innoviva's Triple Combo Therapy Gets FDA Nod For COPD

 | Sep 19, 2017 03:05AM ET

GlaxoSmithKline plc (NYSE:GSK) and partner Innoviva, Inc. (NASDAQ:INVA) announced that the FDA has approved a once-daily, single inhaler triple combination therapy — FF/UMEC/VI (fluticasone furoate/umeclidinium/vilanterol) — as maintenance treatment for patients with chronic obstructive pulmonary disease (COPD). The drug is approved under the brand name, Trelegy Ellipta. The company said that the medicine will be available in the United States shortly.

While fluticasone furoate is an inhaled corticosteroid (ICS), umeclidinium is a long-acting muscarinic antagonist (LAMA) and vilanterol is a long-acting beta2-adrenergic agonist (LABA). This combination medicine will be delivered once daily in the Ellipta dry powder inhaler. Typically, the ICS/LAMA/LABA amalgamation for advanced COPD is delivered via two or more inhalers with potentially differing dose regime. However, GlaxoSmithKline’s triple therapy combination offers a daily treatment in a single Ellipta inhaler.

Notably, closed triple combination therapy is not licensed as a single inhaler triple therapy anywhere outside the United States.

GlaxoSmithKline’s shares are up 4% so far this year, comparing unfavorably with the 16.4% rally of the industry during the period.