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DC Field | Value | Language |
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dc.contributor.author | Bomback A.S. | - |
dc.contributor.author | Daina E. | - |
dc.contributor.author | Remuzzi G. | - |
dc.contributor.author | Kanellis J. | - |
dc.contributor.author | Kavanagh D. | - |
dc.contributor.author | Pickering M.C. | - |
dc.contributor.author | Sunder-Plassmann G. | - |
dc.contributor.author | Walker P.D. | - |
dc.contributor.author | Wang Z. | - |
dc.contributor.author | Ahmad Z. | - |
dc.contributor.author | Fakhouri F. | - |
dc.date.accessioned | 2024-11-22T03:37:34Z | - |
dc.date.available | 2024-11-22T03:37:34Z | - |
dc.date.copyright | 2024 | - |
dc.date.issued | 2024-11-01 | en |
dc.identifier.citation | Kidney International Reports. (no pagination), 2024. Date of Publication: 2024. | - |
dc.identifier.uri | https://repository.monashhealth.org/monashhealthjspui/handle/1/52707 | - |
dc.description.abstract | Introduction: 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.publisher | Elsevier Inc. | - |
dc.relation.ispartof | Kidney International Reports | - |
dc.subject.mesh | electron microscopy | - |
dc.subject.mesh | glomerulopathy | - |
dc.subject.mesh | kidney graft | - |
dc.title | Efficacy and safety of pegcetacoplan in kidney transplant recipients with recurrent complement 3 glomerulopathy or primary immune complex membranoproliferative glomerulonephritis. | - |
dc.type | Article | - |
dc.identifier.affiliation | Nephrology | - |
dc.identifier.affiliation | General Medicine | - |
dc.type.studyortrial | Randomised controlled trial | - |
dc.identifier.doi | https://dx.doi.org/10.1016/j.ekir.2024.09.030 | - |
dc.publisher.place | United 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.openairetype | Article | - |
item.fulltext | No Fulltext | - |
item.cerifentitytype | Publications | - |
item.grantfulltext | none | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
Appears in Collections: | Articles |
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