Glaxo/Innoviva's Trelegy Ellipta Gets Line Extension In Europe

 | Nov 12, 2018 09:22PM ET

GlaxoSmithKline plc (NYSE:GSK) and partner Innoviva, Inc. (NASDAQ:INVA) announced the approval of label expansion of chronic obstructive pulmonary disease (“COPD”) drug, Trelegy Ellipta, in Europe. The drug is now approved as a maintenance treatment in a broader moderate-to-severe COPD patient population those who are not adequately treated by a long-acting muscarinic antagonist (“LAMA”) and long-acting beta2-agonist (“LABA”) or dual bronchodilation.

Trelegy Ellipta, a triple combination therapy of inhaled corticosteroid (“ICS”)/LAMA/LABA (fluticasone furoate/umeclidinium/vilanterol 'FF/UMEC/VI'), is already approved as maintenance treatment for COPD patients who are not adequately treated by a combination of ICS and a LABA.

The label expansion was approved based on data from phase III IMPACT study, which showed that the closed triple combination, Trelegy Ellipta, is superior to ICS-LABA combination, Relvar/Breo Ellipta, and LAMA-LABA combination, Anoro Ellipta, in improving lung function and health-related quality of life, and reducing exacerbations in COPD patients. A similar label update was approved by the FDA in April.

GlaxoSmithKline’s shares have gained 15.7% so far this year compared with 8% increase of the industry during the period.