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Abstract: SA-OR051

Zanubrutinib (zanu) in Anti-Phospholipase A2 Receptor (PLA2R)-Associated Primary Membranous Nephropathy (PMN): Preliminary Results of a Phase 2/3, Multicenter, Randomized, Open-Label Study

Session Information

Category: Glomerular Diseases

  • 1402 Glomerular Diseases: Clinical, Outcomes, and Therapeutics

Authors

  • Lafayette, Richard A., Stanford University Medical Center, Stanford, California, United States
  • Barbour, Sean, The University of British Columbia, Vancouver, British Columbia, Canada
  • Chen, Yanyan, BeOne Medicines Ltd, Shanghai, China
  • Yao, Zhen, BeOne Medicines Ltd, Shanghai, China
  • Song, Jingwen, BeOne Medicines Ltd, Shanghai, China
  • Li, Guisen, Sichuan Provincial People’s Hospital, Chengdu, China
  • Zhao, Minghui, Peking University First Hospital, Beijing, Beijing, China
Background

BTK plays a role in B-cell modulation and is a potential target in PMN. Zanu (BTK inhibitor) is being evaluated in a 2-part study in PMN (NCT05707377). Part 1 data are shown.

Methods

After a 12-wk run-in, pts with PLA2R antibody >50 RU/mL and urinary protein-creatinine ratio (UPCR) >3.5 g/g received zanu 160 mg twice daily for 64 wks, followed by 40-wk observation. The efficacy endpoints include change from baseline in anti-PLA2R antibody titer, UPCR, clinical remission rate and safety.

Results

As of March 7, 2025, 30 pts were treated; median age: 46.5 (range 32-74) yrs, 66.7% male, 90.0% were from Asia. At baseline, mean UPCR was 7.8 mg/mg (SD 3.0), median serum anti-PLA2R antibody was 161.0 RU/mL (range 51.4-1219.8), mean serum albumin was 25.4 g/L (SD 7.2), median eGFR was 85.2 mL/min/1.73m2 (range 39.8-123.0). Median exposure: 57 wks. At 52 wks, mean UPCR change from baseline: -4.9 mg/mg (SD 2.5), a 70.4% reduction overall (Fig 1). 5 pts had complete remission (UPCR ≤0.3 mg/mg and stable eGFR) and 8 pts had partial remission (UPCR of >0.3 to ≤3.5 mg/mg, with ≥50% decrease from baseline, and stable eGFR), resulting in a total remission rate of 43.3%. Fig 2: change in PLA2R antibody. Immunological response rate (anti-PLA2R titer reduction to <14 RU/mL) was 56.7%. 27 pts (90.0%) had treatment-emergent adverse events (TEAEs); most common: upper respiratory tract infection (30.0%), rash, anemia (both 23.3%). Four pts (13.3%) had severe TEAEs (two treatment-related).

Conclusion

Zanu is generally well tolerated with promising efficacy in pts with primary PMN; continued evaluation in pts with PMN is supported.

Funding

  • Commercial Support – BeOne Medicines Ltd

Digital Object Identifier (DOI)