Diurnal gets first drug approval by US FDA
The US Food and Drug Administration has approved Alkindi Sprinkle (hydrocortisone oral granules) as replacement therapy in pediatric patients with adrenocortical insufficiency (AI) from UK specialty pharma company Diurnal (AIM: DNL), making it only the third listed AIM company to obtain FDA approval for a product, according to Hardman research, and sending Diurnal’s shares up 10.5% to 72.90 pence by late morning.
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