C5a receptor inhibitor avacopan in immunoglobulin A nephropathy—an open-label pilot study

Author:

Bruchfeld Annette12ORCID,Magin Hasan2,Nachman Patrick3,Parikh Samir4,Lafayette Richard5,Potarca Antonia6,Miao Shichang6,Bekker Pirow6

Affiliation:

1. Department of Health, Medicine and Caring Sciences, Linköping University, Linköping, Sweden

2. Department of Renal Medicine, Karolinska University Hospital and CLINTEC Karolinska Institutet, Stockholm, Sweden

3. Division of Renal Diseases and Hypertension, Minneapolis, University of Minnesota, Minneapolis, MN, USA

4. Department of Nephrology, Ohio State University Wexner Medical Center, Columbus, OH, USA

5. Department of Nephrology, Stanford University, Palo Alto, CA, USA

6. ChemoCentryx, San Carlos, CA, USA

Abstract

ABSTRACT Background Improvement of proteinuria as a marker for disease activity is associated with a better renal outcome in immunoglobulin A nephropathy (IgAN). Complement is an effector pathway in IgA-mediated kidney injury. Avacopan, a selective C5a receptor inhibitor, has previously shown efficacy in anti-neutrophil cytoplasmic antibody–associated vasculitis. The aim of this study was to evaluate the safety and efficacy of avacopan in patients with IgAN with persistent proteinuria despite a maximally tolerated dose of renin–angiotensin–aldosterone system blockade. The efficacy evaluation was based on the change in proteinuria. Methods This open-label pilot trial enrolled adult patients with biopsy-proven IgAN, urinary protein:creatinine ratio (UPCR) >1 g/g creatinine and an estimated glomerular filtration rate (eGFR) >60 mL/min/1.73 m2 or >45 mL/min/1.73 m2 if eGFR has not declined >10 mL/min/1.73 m2 over the previous 24 weeks. If the UPCR remained at >1 g/g creatinine after an 8-week run-in period, patients started avacopan 30 mg twice daily. The primary efficacy endpoint was the change in the slope of the UPCR from the 8-week run-in period to the slope in the 12-week avacopan dosing period. Results A total of 10 of 15 screened patients entered the run-in period. Seven patients with a UPCR >1 g/g creatinine received avacopan. Six of seven patients had numerical improvement in the UPCR during the avacopan treatment period, three of whom had a numerical improvement of ∼50% at week 12. At week 24, five of seven patients still showed numerical improvement in the UPCR compared with baseline. The urinary monocyte chemoattractant protein-1:creatinine ratio decreased numerically 30% by week 8, possibly reflecting the anti-inflammatory activity of avacopan. Avacopan was well tolerated. There was one serious adverse event of unstable angina, which was deemed to be unrelated to avacopan. Conclusions This short-term pilot study showed an improvement in the slope of the UPCR, with ∼50% improvement in three of seven patients with IgAN. Longer avacopan treatment duration may be indicated for maximal benefit.

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

Reference27 articles.

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2. Epidemiologic data of renal diseases from a single unit in China: analysis based on 13,519 renal biopsies;Li;Kidney Int,2004

3. IgA nephropathy;Wyatt;N Engl J Med,2013

4. The pathophysiology of IgA nephropathy;Hitoshi;J Am Soc Nephrol,2011

5. The MEST score provides earlier risk prediction in IgA nephropathy;Barbour;Kidney Int,2016

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