European regulators OK Uptravi after safety review

7 April 2017

The European Medicines Agency (EMA) has given Switzerland-based Actelion (SIX: ATLN) the OK to continue selling Uptravi (selexipag), after five patient deaths in France triggered a safety review.

The EMA has confirmed that the therapy can continue to be used by both new and existing patients, and that no changes to the prescribing information are required.

The drug, which received marketing authorization in the European Union a year ago, is used to treat pulmonary arterial hypertension (PAH), a life-threatening condition involving abnormally high blood pressure in the arteries of the lungs.

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