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A Randomized, Double-Blind, Placebo Controlled Study to Evaluate Efficacy and Safety of Nefecon in Patients with Primary IgA Nephropathy at Risk of Progressing to End-Stage Renal Disease (NefIgArd)

Trial Profile

A Randomized, Double-Blind, Placebo Controlled Study to Evaluate Efficacy and Safety of Nefecon in Patients with Primary IgA Nephropathy at Risk of Progressing to End-Stage Renal Disease (NefIgArd)

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 12 Jun 2025

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At a glance

  • Drugs Budesonide (Primary)
  • Indications IgA nephropathy
  • Focus Registrational; Therapeutic Use
  • Acronyms NefIgArd
  • Sponsors Calliditas Therapeutics

Most Recent Events

  • 09 Jun 2025 According to Calliditas Therapeutics media release, data from this trial presented at the 62nd European Renal Association Congress (ERA Congress)
  • 07 May 2025 Results presented in an Everest Medicines media release.
  • 07 May 2025 According to an Everest Medicines media release, the company announced that the supplemental New Drug Application (sNDA) for NEFECON has received full approval from the China National Medical Products Administration (NMPA). The NMPA's full approval is supported by robust efficacy and safety data from this study.

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