KalVista (KALV) Pharmaceuticals announced that the U.S. Food and Drug Administration has approved EKTERLY, a novel plasma kallikrein inhibitor, for the treatment of acute attacks of hereditary angioedema in adult and pediatric patients aged 12 years and older. EKTERLY is the first and only oral on-demand treatment for HAE. KalVista will launch EKTERLY in the U.S. immediately and physicians can begin writing prescriptions today.
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