Zealand Pharma initiates second Phase 3 trial with dasiglucagon for the treatment of congenital hyperinsulinism
Zealand Pharma A/S - American Depositary Shares (ZEAL)
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Source: GlobeNewswire
Press Release – No. 21 / 2019 Zealand Pharma initiates second Phase 3 trial with dasiglucagon for the treatment of congenital hyperinsulinism Congenital hyperinsulinism (CHI) is a rare pediatric disease with high unmet medical needs and serious, debilitating lifelong complications This Phase 3 trial will evaluate dasiglucagon as treatment for CHI children ages 7 days to 1 year who are dependent on intravenous glucose infusions Dasiglucagon has been granted a Rare Pediatric Disease designation by the FDA for treatment of CHI in November 2019 Copenhagen, December 4, 2019 – Zealand Pharma A/S ("Zealand") (NASDAQ: ZEAL), a Copenhagen-based biotechnology company focused on the discovery and development of innovative peptide-based medicines, today announced that the second Phase 3 trial to evaluate dasiglucagon as a potential treatment option for children with congenital hyperinsulinism (CHI) has been initiated. This Phase 3 trial will enroll up to 12 CHI children
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