US FDA extends review of KalVista's swelling disorder drug due to heavy workload
June 13 (Reuters) - The U.S. Food and Drug Administration extended the review of KalVista Pharmaceuticals' KALV.O drug for a type of hereditary swelling disorder due to heavy workload and limited resources, the company said on Friday.
The FDA indicated that it expects to deliver a decision within approximately four weeks, KalVista said.
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