AstraZeneca's Once-Weekly Diabetes Med Wins FDA Nod For Use In Children

  • The FDA has approved AstraZeneca Plc's AZN Budureon BCise (exenatide extended-release), once-weekly injectable suspension for type 2 diabetes (T2D) in pediatric patients (10 to 17 years) as an adjunct to diet and exercise.
  • The approval was supported by the positive results of the BCB114 Phase 3 trial, which showed that on top of standard of care, exenatide extended-release significantly improved glycemic control compared to placebo in pediatrics.
  • This is the first completed trial of a once-weekly GLP-1 RA in a pediatric population with T2D, the Company said in the press release.
  • Price Action: AZN shares are up 0.21% at $58.37 during the premarket session on the last check Friday.
  • Related content: Benzinga's Full FDA Calendar.
Market News and Data brought to you by Benzinga APIs
Comments
Loading...
Posted In: BiotechNewsHealth CareFDAGeneralBriefsDiabetes
Benzinga simplifies the market for smarter investing

Trade confidently with insights and alerts from analyst ratings, free reports and breaking news that affects the stocks you care about.

Join Now: Free!