Friday, October 23, 2009

Movetis obtains EU authorisation for the commercialisation of Resolor (prucalopride)

October 23, 2009 - Movetis, the GI specialty pharmaceutical company based in Belgium, announces that it has obtained approval from the European Commission for the commercialisation of its lead product Resolor (prucalopride – a 1mg and 2mg once a day oral tablet) for the symptomatic treatment of chronic constipation (CC) in women in whom laxatives fail to provide adequate relief.

The details can be read here.

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