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Developing Therapies for C3 Glomerulopathy: Report of the Kidney Health Initiative C3 Glomerulopathy Trial Endpoints Work Group.
Nester, Carla; Decker, Dima A; Meier, Matthias; Aslam, Shakil; Bomback, Andrew S; Caravaca-Fontán, Fernando; Cook, Terence H; Feldman, David L; Fremeaux-Bacchi, Veronique; Gale, Daniel P; Gooch, Ann; Johnson, Sally; Licht, Christoph; Mathur, Mohit; Pickering, Matthew C; Praga, Manuel; Remuzzi, Giuseppe; Selvarajah, Viknesh; Smith, Richard J; Tabriziani, Hossein; van de Kar, Nicole; Wang, Yaqin; Wong, Edwin; Mistry, Kirtida; Lim, Mark; Portillo, Cesia; Balogun, Seyi; Trachtman, Howard; Thompson, Aliza.
Affiliation
  • Nester C; Department of Pediatrics, Division of Nephrology, Carver College of Medicine, University of Iowa, Iowa City, Iowa.
  • Decker DA; Apellis Pharmaceuticals Inc., Waltham, Massachusetts.
  • Meier M; Novartis Inc., Basel, Switzerland.
  • Aslam S; BioCryst Pharmaceuticals Inc., Durham, North Carolina.
  • Bomback AS; Columbia University Irving Medical Center, New York, New York.
  • Caravaca-Fontán F; Research Institute "Hospital 12 de Octubre," Madrid, Spain.
  • Cook TH; Department of Immunology and Inflammation, Imperial College London, London, United Kingdom.
  • Feldman DL; National Kidney Foundation, New York, New York.
  • Fremeaux-Bacchi V; Hôpital Europeén Georges Pompidou, Paris, France.
  • Gale DP; Department of Renal Medicine, University College of London, London, United Kingdom.
  • Gooch A; Rare Kidney Disease Registry (RaDaR), Bristol, United Kingdom.
  • Johnson S; BioCryst Pharmaceuticals Inc., Durham, North Carolina.
  • Licht C; Great North Children's Hospital, Newcastle upon Tyne, United Kingdom.
  • Mathur M; The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Pickering MC; Visterra Inc., Waltham, Massachusetts.
  • Praga M; Department of Immunology and Inflammation, Imperial College London, London, United Kingdom.
  • Remuzzi G; Department of Medicine, Nephrology Department, Complutense University, Madrid, Spain.
  • Selvarajah V; Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Bergamo, Italy.
  • Smith RJ; Research and Early Development, Cardiovascular, Renal and Metabolism, Biopharmaceuticals R&D, AstraZeneca, Cambridge, United Kingdom.
  • Tabriziani H; Molecular Otolaryngology and Renal Research Laboratories, Carver College of Medicine, University of Iowa, Iowa City, Iowa.
  • van de Kar N; Natera Inc., Austin, Texas.
  • Wang Y; Radboud Institute for Molecular Life Sciences, Amalia Children's Hospital, Radboud University, Nijmegen, The Netherlands.
  • Wong E; Novartis Inc., East Hanover, New Jersey.
  • Mistry K; Translational and Clinical Research Institute, Newcastle University, Newcastle Upon Tyne, United Kingdom.
  • Lim M; Center for the Drug Evaluation and Research, US Food and Drug Administration, Silver Spring, Maryland.
  • Portillo C; Kidney Health Initiative, American Society of Nephrology, Washington, DC.
  • Balogun S; Kidney Health Initiative, American Society of Nephrology, Washington, DC.
  • Trachtman H; Kidney Health Initiative, American Society of Nephrology, Washington, DC.
  • Thompson A; Department of Pediatrics, University of Michigan, Ann Arbor, Michigan.
Article in En | MEDLINE | ID: mdl-38829708
ABSTRACT
Randomized clinical trials are underway to evaluate the efficacy of novel agents targeting the alternative complement pathway in patients with C3 glomerulopathy (C3G), a rare glomerular disease. The Kidney Health Initiative convened a panel of experts in C3G to ( 1 ) assess the data supporting the use of the prespecified trial end points as measures of clinical benefit and ( 2 ) opine on efficacy findings they would consider compelling as treatment(s) of C3G in native kidneys. Two subpanels of the C3G Trial Endpoints Work Group reviewed the available evidence and uncertainties for the association between the three prespecified end points-( 1 ) proteinuria, ( 2 ) eGFR, and ( 3 ) histopathology-and anticipated outcomes. The full work group provided feedback on the summaries provided by the subpanels and on what potential treatment effects on the proposed end points they would consider compelling to support evidence of an investigational product's effectiveness for treating C3G. Members of the full work group agreed with the characterization of the data, evidence, and uncertainties, supporting the end points. Given the limitations of the available data, the work group was unable to define a minimum threshold for change in any of the end points that might be considered clinically meaningful. The work group concluded that a favorable treatment effect on all three end points would provide convincing evidence of efficacy in the setting of a therapy that targeted the complement pathway. A therapy might be considered effective in the absence of complete alignment in all three end points if there was meaningful lowering of proteinuria and stabilization or improvement in eGFR. The panel unanimously supported efforts to foster data sharing between academic and industry partners to address the gaps in the current knowledge identified by the review of the end points in the aforementioned trials.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Clin J Am Soc Nephrol Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Clin J Am Soc Nephrol Year: 2024 Document type: Article