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Improving Clinical Trials for Anticomplement Therapies in Complement-Mediated Glomerulopathies: Report of a Scientific Workshop Sponsored by the National Kidney Foundation.
Bomback, Andrew S; Appel, Gerald B; Gipson, Debbie S; Hladunewich, Michelle A; Lafayette, Richard; Nester, Carla M; Parikh, Samir V; Smith, Richard J H; Trachtman, Howard; Heeger, Peter S; Ram, Sanjay; Rovin, Brad H; Ali, Shadab; Arceneaux, Nicole; Ashoor, Isa; Bailey-Wickins, Laura; Barratt, Jonathan; Beck, Laurence; Cattran, Daniel C; Cravedi, Paolo; Erkan, Elif; Fervenza, Fernando; Frazer-Abel, Ashley A; Fremeaux-Bacchi, Veronique; Fuller, Lindsey; Gbadegesin, Rasheed; Hogan, Jonathan J; Kiryluk, Krzysztof; le Quintrec-Donnette, Moglie; Licht, Christoph; Mahan, John D; Pickering, Matthew C; Quigg, Richard; Rheault, Michelle; Ronco, Pierre; Sarwal, Minnie M; Sethna, Christine; Spino, Cathie; Stegall, Mark; Vivarelli, Marina; Feldman, David L; Thurman, Joshua M.
Afiliação
  • Bomback AS; Division of Nephrology, Columbia University Irving Medical Center, New York. Electronic address: asb68@cumc.columbia.edu.
  • Appel GB; Division of Nephrology, New York University Langone Health, New York.
  • Gipson DS; Department of Pediatrics, Division of Nephrology, University of Michigan, Ann Arbor, Michigan.
  • Hladunewich MA; Division of Nephrology, Sunnybrook Health Sciences Centre, Toronto, ON, Canada.
  • Lafayette R; Division of Nephrology, Stanford University, Stanford, California.
  • Nester CM; Division of Nephrology, University of Iowa, Iowa City, Iowa.
  • Parikh SV; Division of Nephrology, The Ohio State University College of Medicine, Columbus, Ohio.
  • Smith RJH; Department of Molecular Physiology and Biophysics, University of Iowa, Iowa City, Iowa.
  • Trachtman H; Division of Nephrology, New York University Langone Health, New York.
  • Heeger PS; Division of Nephrology, Icahn School of Medicine at Mount Sinai, New York.
  • Ram S; Division of Infectious Diseases and Immunology, University of Massachusetts Medical School, Worcester, Massachusetts.
  • Rovin BH; Division of Nephrology, The Ohio State University College of Medicine, Columbus, Ohio.
  • Ali S; National Kidney Foundation, New York.
  • Arceneaux N; National Kidney Foundation, New York.
  • Ashoor I; Division of Nephrology, Louisiana State University Health, New Orleans, Louisiana.
  • Bailey-Wickins L; National Kidney Foundation, New York.
  • Barratt J; Division of Nephrology, University of Leicester, Leicester.
  • Beck L; Division of Nephrology, Boston University School of Medicine, Boston, Massachusetts.
  • Cattran DC; Division of Nephrology, University of Toronto, Toronto, ON, Canada.
  • Cravedi P; Division of Nephrology, Icahn School of Medicine at Mount Sinai, New York.
  • Erkan E; Division of Nephrology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • Fervenza F; Division of Nephrology, Mayo Clinic, Rochester.
  • Frazer-Abel AA; Division of Nephrology, University of Colorado School of Medicine, Aurora, Colorado.
  • Fremeaux-Bacchi V; Division of Nephrology, Université de Paris, Paris.
  • Fuller L; National Kidney Foundation, New York.
  • Gbadegesin R; Division of Nephrology, Duke University, Durham, North Carolina.
  • Hogan JJ; Division of Nephrology, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Kiryluk K; Division of Nephrology, Columbia University Irving Medical Center, New York.
  • le Quintrec-Donnette M; Division of Nephrology, Centre Hospitalier Universitaire de Montpellier, Montpellier, France.
  • Licht C; Division of Nephrology, University of Toronto, Toronto, ON, Canada.
  • Mahan JD; Division of Nephrology, The Ohio State University College of Medicine, Columbus, Ohio.
  • Pickering MC; Division of Nephrology, Imperial College London, London, United Kingdom.
  • Quigg R; Division of Nephrology, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, New York.
  • Rheault M; Division of Nephrology, University of Minnesota, Minneapolis, Minnesota.
  • Ronco P; Division of Nephrology, Sorbonne Université, Université Pierre et Marie Curie, Paris.
  • Sarwal MM; Division of Nephrology, University of California, San Francisco, California.
  • Sethna C; Division of Nephrology, Donald and Barbara Zucker School of Medicine at Hofstra/Northwell, Hempstead, New York.
  • Spino C; Department of Biostatistics, University of Michigan, Ann Arbor, Michigan.
  • Stegall M; Division of Nephrology, Mayo Clinic, Rochester.
  • Vivarelli M; Division of Nephrology, Bambino Gesu Children's Hospital, Rome, Italy.
  • Feldman DL; National Kidney Foundation, New York.
  • Thurman JM; Division of Nephrology, University of Colorado School of Medicine, Aurora, Colorado.
Am J Kidney Dis ; 79(4): 570-581, 2022 04.
Article em En | MEDLINE | ID: mdl-34571062
Blocking the complement system as a therapeutic strategy has been proposed for numerous glomerular diseases but presents myriad questions and challenges, not the least of which is demonstrating efficacy and safety. In light of these potential issues and because there are an increasing number of anticomplement therapy trials either planned or under way, the National Kidney Foundation facilitated an all-virtual scientific workshop entitled "Improving Clinical Trials for Anti-Complement Therapies in Complement-Mediated Glomerulopathies." Attended by patient representatives and experts in glomerular diseases, complement physiology, and clinical trial design, the aim of this workshop was to develop standards applicable for designing and conducting clinical trials for anticomplement therapies across a wide spectrum of complement-mediated glomerulopathies. Discussions focused on study design, participant risk assessment and mitigation, laboratory measurements and biomarkers to support these studies, and identification of optimal outcome measures to detect benefit, specifically for trials in complement-mediated diseases. This report summarizes the discussions from this workshop and outlines consensus recommendations.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas Inativadoras do Complemento / Nefropatias Tipo de estudo: Guideline / Risk_factors_studies Aspecto: Patient_preference Limite: Humans Idioma: En Revista: Am J Kidney Dis Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas Inativadoras do Complemento / Nefropatias Tipo de estudo: Guideline / Risk_factors_studies Aspecto: Patient_preference Limite: Humans Idioma: En Revista: Am J Kidney Dis Ano de publicação: 2022 Tipo de documento: Article
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