KalVista reports PhIII success of on-demand, oral hereditary angioedema drug as it seeks to challenge injectables
KalVista Pharmaceuticals’ oral medicine for hereditary angioedema helped relieve attack symptoms associated with the disease substantially faster than placebo in a late-stage study, setting the company up to submit for an FDA approval this year.
In hereditary angioedema, or HAE for short, people experience severe swelling attacks. Currently, the attacks are treated with injectable medicines such as Takeda’s Firazyr, but KalVista hopes its pill can provide an easier and potentially quicker option.
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