GlaxoSmithKline files for umeclidinium monotherapy approval in Europe

29 April 2013

UK pharma giant GlaxoSmithKline (LSE: GSK) has submitted a regulatory application in the European Union for the investigational once-daily medicine, umeclidinium bromide (UMEC), for patients with chronic obstructive pulmonary disease (COPD).

UMEC is an investigational bronchodilator molecule (formerly known as GSK573719), a long-acting muscarinic antagonist (LAMA), administered using the Ellipta inhaler, under development with the USA’s Theravance (Nasdaq: THRX), which has just announced its intention to split into two separate publicly traded company (see separate story today)

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