Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/52707
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dc.contributor.authorBomback A.S.-
dc.contributor.authorDaina E.-
dc.contributor.authorRemuzzi G.-
dc.contributor.authorKanellis J.-
dc.contributor.authorKavanagh D.-
dc.contributor.authorPickering M.C.-
dc.contributor.authorSunder-Plassmann G.-
dc.contributor.authorWalker P.D.-
dc.contributor.authorWang Z.-
dc.contributor.authorAhmad Z.-
dc.contributor.authorFakhouri F.-
dc.date.accessioned2024-11-22T03:37:34Z-
dc.date.available2024-11-22T03:37:34Z-
dc.date.copyright2024-
dc.date.issued2024-11-01en
dc.identifier.citationKidney International Reports. (no pagination), 2024. Date of Publication: 2024.-
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/52707-
dc.description.abstractIntroduction: Complement 3 glomerulopathy (C3G) and primary immune complex membranoproliferative glomerulonephritis (IC-MPGN) have high risks for disease recurrence and allograft loss in transplant kidneys. Pegcetacoplan (targeted complement 3 [C3]/C3b inhibitor) may prevent excessive deposition of C3 and complement 5 [C5] breakdown products and associated renal damage. Method(s): NOBLE (NCT04572854) is a prospective, phase 2, multicenter, open-label, randomized controlled trial evaluating the efficacy and safety of pegcetacoplan in posttransplant patients with recurrent C3G or IC-MPGN. The primary end point was reduction in C3c staining on renal biopsy at week 12 for patients who received either pegcetacoplan 1080 mg twice weekly by subcutaneous infusion plus standard-of-care (SOC) or SOC only. Result(s): Ten patients received pegcetacoplan and 3 received SOC only through week 12. At week 12, 5 of 10 pegcetacoplan-treated patients (50%) achieved >=2 orders of magnitude (OOM) reduction in C3 staining (4 of these 5 had 0 staining and absent electron microscopy deposits) and 8 of 10 (80%) achieved >=1 OOM reduction; 1 of 3 (33%) SOC-only patients showed staining reduction. Mean C3G histology activity score decreased by >54% in 8 of 10 pegcetacoplan-treated patients (80.0%). Pegcetacoplan-treated patients with baseline urine protein-to-creatinine ratio (uPCR) >=1000 mg/g showed a median (interquartile range [IQR]) 54.4% (-56.33 to -53.95) reduction in proteinuria at week 12. In addition, pegcetacoplan-treated patients showed stable estimated glomerular filtration rate (eGFR), reduced plasma sC5b-9, and increased serum C3. Pegcetacoplan was well-tolerated and most adverse events were mild/moderate. No discontinuations, treatment withdrawals, or deaths were reported. Conclusion(s): NOBLE demonstrated efficacy, safety, and tolerability of pegcetacoplan for patients with posttransplant recurrent C3G and primary IC-MPGN.Copyright © 2024 International Society of Nephrology-
dc.publisherElsevier Inc.-
dc.relation.ispartofKidney International Reports-
dc.subject.meshelectron microscopy-
dc.subject.meshglomerulopathy-
dc.subject.meshkidney graft-
dc.titleEfficacy and safety of pegcetacoplan in kidney transplant recipients with recurrent complement 3 glomerulopathy or primary immune complex membranoproliferative glomerulonephritis.-
dc.typeArticle-
dc.identifier.affiliationNephrology-
dc.identifier.affiliationGeneral Medicine-
dc.type.studyortrialRandomised controlled trial-
dc.identifier.doihttps://dx.doi.org/10.1016/j.ekir.2024.09.030-
dc.publisher.placeUnited States-
dc.identifier.institution(Bomback) Division of Nephrology, Columbia University Irving Medical Center, New York, NY, United States-
dc.identifier.institution(Daina, Remuzzi) Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Bergamo, Italy-
dc.identifier.institution(Kanellis) Department of Nephrology, Monash Health and Centre for Inflammatory Diseases, Clayton, Australia-
dc.identifier.institution(Kanellis) Department of Medicine, Monash Medical Centre, Clayton, Australia-
dc.identifier.institution(Kavanagh) National Renal Complement Therapeutics Centre, Newcastle University, United Kingdom-
dc.identifier.institution(Pickering) Imperial College, London, United Kingdom-
dc.identifier.institution(Sunder-Plassmann) Division of Nephrology and Dialysis, Department of Medicine III, Medical University of Vienna, Vienna, Austria-
dc.identifier.institution(Walker) Department of Renal Pathology, Arkana Laboratories, Little Rock, AR, United States-
dc.identifier.institution(Wang, Ahmad) Apellis Pharmaceuticals, Inc., Waltham, MA, United States-
dc.identifier.institution(Fakhouri) Lausanne University Hospital, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland-
dc.identifier.affiliationmh(Kanellis) Department of Nephrology, Monash Health and Centre for Inflammatory Diseases, Clayton, Australia-
dc.identifier.affiliationmh(Kanellis) Department of Medicine, Monash Medical Centre, Clayton, Australia-
item.openairetypeArticle-
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
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