Zealand Pharma to seek FDA approval of its treatment for rare genetic disorder in babies

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Zealand Pharma to seek FDA approval of its treatment for rare genetic disorder in babies
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U.S.-listed shares of Zealand Pharma undefinedundefined soared 21.2% in premarket trading on Thursday after the company said a Phase 3 clinical trial...

U.S.-listed shares of Zealand Pharma soared 21.2% in premarket trading on Thursday after the company said a Phase 3 clinical trial evaluating its investigational treatment for babies with a rare genetic disorder met the primary endpoint. Zealand is testing dasiglucagon as a treatment for pediatric patients with congenital hyperinsulinism, which causes excess insulin secretion and low blood sugar.

2% in premarket trading on Thursday after the company said a Phase 3 clinical trial evaluating its investigational treatment for babies with a rare genetic disorder met the primary endpoint. Zealand is testing dasiglucagon as a treatment for pediatric patients with congenital hyperinsulinism, which causes excess insulin secretion and low blood sugar.

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