Core Viewpoint - The latest research presented at the ERA 2025 conference demonstrates that NefECON (budesonide delayed-release capsules) provides significant clinical benefits when used early in the treatment of IgA nephropathy, supporting a new management strategy focused on early and targeted treatment [1][2][3] Group 1: Research Findings - Eight oral presentations and one electronic poster were showcased, with two studies confirming the clinical benefits of early treatment with NefECON for IgA nephropathy [1] - A sub-analysis of the NefIgArd study indicated that budesonide significantly reduces proteinuria and protects kidney function across different diagnosis times, with more pronounced benefits in patients diagnosed within 0.6 years [2][3] - A prospective study showed that early use of budesonide not only reduces pathogenic IgA production but also may help control inflammatory responses, thereby slowing disease progression [2] Group 2: Clinical Implications - The findings emphasize the importance of early intervention in IgA nephropathy treatment, providing strong evidence for clinical practice [2] - The 2025 version of the "Clinical Practice Guidelines for Adult IgA Nephropathy and IgA Vasculitis" in China recommends budesonide as the first choice for reducing pathogenic IgA [2] - NefECON has been included in both the KDIGO and Chinese clinical practice guidelines, highlighting its significance as a treatment option [12] Group 3: Company Positioning - NefECON is the first and only drug for targeted treatment of IgA nephropathy approved in China, the US, and Europe, marking a shift in treatment standards [2][12] - The drug has shown the potential to delay kidney function decline by 66% in the Chinese population and extend the time to dialysis or kidney transplant by 12.8 years [13] - The company has secured full approval for NefECON in China, removing previous restrictions related to proteinuria levels [2]