Panelists discuss how the APPEAR-C3G trial demonstrated that iptacopan significantly reduced proteinuria by 35% at 6 months, was well tolerated with no new safety signals over 12 months, slowed glomerular filtration rate (GFR) decline, and showed a statistically significant reduction in glomerular C3 deposit scores, though detailed biopsy clearance rates were not reported.
Enrolled approximately 70 patients with biopsy-proven C3G, proteinuria >1g/day, GFR >30 mL/min, and low serum C3 levels
Primary Outcome
35% reduction in proteinuria at 6 months, statistically significant and sustained through 12 months
No new safety signals in open-label extension
Historical comparisons suggest iptacopan attenuates GFR decline
Biopsy and Histologic Findings
Study used a unique glomerular C3 deposit score, not standard in clinical practice, including C3 breakdown products
Significant reduction in C3 deposits in the treatment group (P = .0005), whereas placebo group showed worsening
Data on complete C3 clearance (e.g., 3+ to 0) were not made publicly available
Notable Observations
Dense deposit disease (DDD), considered a more aggressive subtype, was overrepresented in the treatment arm (9 of 10 patients), suggesting efficacy despite a bias toward more severe disease.
Use of low serum C3 as an inclusion criterion aimed to demonstrate mechanism of action (complement inhibition), though this may have excluded patients with normal C3 but active disease.
Conclusion Iptacopan demonstrated clear efficacy in reducing proteinuria, improving complement activity markers, and possibly slowing renal function decline in C3G. The trial supports its safety and potential role in managing patients with complement-driven glomerulopathies.