FDA approves selexipag for IV use in adults with PAH

The FDA has approved selexipag for IV use in adults with WHO functional class II to III pulmonary arterial hypertension who are temporarily unable to take oral therapy. Selexipag (Uptravi, Janssen) for IV use will allow patients to avoid short-term interruptions and stay on their therapy, as uninterrupted treatment is important for patients with PAH, according to a company press release.

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