Novartis’ skin disease drug gets US FDA approval

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(Reuters) -The U.S. Food and Drug Administration has approved Novartis’ oral treatment for patients with type of chronic inflammatory skin disease, the company said on Tuesday.

The twice-daily pill, Rhapsido, is approved for patients who have symptoms of chronic spontaneous urticaria (CSU) despite standard therapies.

CSU is a long-term skin condition without a known cause, characterized by recurring hives – itchy, red welts – and sometimes swelling, lasting six weeks or more.

Novartis has completed regulatory submissions in the European Union and Japan, and a priority review has been granted in China, it said.

(Reporting by Siddhi Mahatole in Bengaluru; Editing by Sahal Muhammed)

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