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Vanda CEO Mihael Polymeropoulos called the drug a “familiar therapeutic agent that offers flexible dosing with a well-known safety profile.” April 1 Product: AstraZeneca’s Voydeya Indication: Paroxysmal nocturnal haemoglobinuria AstraZeneca kicked off April with a win for its rare disease portfolio as the FDA approved Voydeya, an oral, first-in-class factor D inhibitor to treat a subset of patients with paroxysmal nocturnal haemoglobinuria (PNH)