AcuCort submits Initial Pediatric Study Plan (iPSP) to the FDA
AcuCort, a pharmaceutical company, has submitted its Initial Pediatric Study Plan (iPSP) to the U.S. Food and Drug Administration (FDA) as part of its regulatory pathway for obtaining FDA approval of Zeqmelit® in 2025.The submission of the iPSP represents a key milestone in the regulatory process to secure market authorization for Zeqmelit® in the United States. The FDA mandates that all companies seeking approval for new drug applications (NDAs) submit an iPSP as part of the approval process. “This submission marks an important step forward in our efforts to make Zeqmelit® accessible to