Slow-Release Jab for Child Growth Hormone Deficiency Gets FDA Nod

Published on

The FDA has given the green light to Danish company Ascendis Pharma for the first slow-release formulation that provides a weekly alternative to daily injections for children with growth hormone deficiency.


For decades, patients with growth hormone deficiency have required tedious daily hormone injections to stave off the effects of the rare condition, including slow growth in children and high levels of body fat in adults. However, the last two years have seen approvals of slow-release formulations that reduce the injection requirement to once a week.

Last year, the FDA approved the first weekly slow-release form of growth hormone in adults with growth hormone deficiency: Novo Nordisk’s Sogroya. An EU approval of Sogroya followed earlier this year.

Then last week, Ascendis Pharma received the FDA’s blessing to market its slow-release hormone therapy Skytrofa for growth hormone deficiency — in this case in children. The Danish company’s stocks have soared by 25% since the approval, and an EU decision is expected later this year.

Long-acting sustained-release technologies have been the holy grail in the delivery of hormones,” said Antoine Papiernik, Chairman and Managing Partner at one of Ascendis’ early investors, Sofinnova Partners. This has the potential to dramatically improve the lives of patients.”

Meanwhile, Pfizer’s own weekly slow-release candidate Somatrogon is set to compete with Skytrofa in the child form of growth hormone deficiency. The drug is expected to have an FDA approval decision by the end of the year. 


For more news from the world of long-acting therapeutics, sign up to the CELT mailing list for regular updates.