The drug is a combination of UMEC, a long-acting
muscarinic antagonist, and VI, a long-acting beta agonist, in a
single inhaler. It is expected to generate sales of more than $2
billion a year by 2018, according to the average estimate of six
analysts polled by Thomson Reuters.
Recommendations for marketing approval from the European Medicines
Agency are usually followed by the granting of full marketing
authorization by the European Commission.
The companies said they expected that decision during the second
quarter of 2014.
The drug, in a different strength formulation, was approved by
regulators in the United States and Canada in December 2013.
(Reporting by Paul Sandle, editing by
Sarah Young)
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