Actelion's Uptravi receives EC marketing nod for PAH

17 May 2016

Switzerland-based Actelion (SIX: ATLN) has received European Commission marketing authorization for Uptravi (selexipag), its selective IP prostacyclin receptor agonist, as a long-term treatment of pulmonary arterial hypertension (PAH).

Actelion, which is Europe’s largest biotech company, has been licensed for the long-term treatment of PAH in adult patients with WHO functional class (FC) II-III.

It is indicated either as a combination therapy in patients insufficiently controlled with an endothelin receptor antagonist (ERA) and/or a phosphodiesterase type 5 (PDE-5) inhibitor, or as monotherapy in patients who are not candidates for these therapies.

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