KalVista (KALV) announced that the European Commission and Swiss Agency for Therapeutic Products, Swissmedic, have approved Ekterly, a novel, oral plasma kallikrein inhibitor, for the symptomatic treatment of acute attacks of hereditary angioedema in adults and adolescents aged 12 years and older.
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Read More on KALV:
- Strong Initial Sales and Medical Endorsement Drive Buy Rating for KalVista Pharmaceuticals’ Ekterly
- Promising Launch of Ekterly Boosts KalVista Pharmaceuticals’ Market Potential
- KalVista price target raised to $28 from $27 at Citizens JMP
- KalVista Pharmaceuticals Reports Strong Start for EKTERLY Launch
- Promising Market Penetration and Growth Potential for KalVista Pharmaceuticals’ Ekterly
