| Literature DB >> 34571062 |
Andrew S Bomback1, Gerald B Appel2, Debbie S Gipson3, Michelle A Hladunewich4, Richard Lafayette5, Carla M Nester6, Samir V Parikh7, Richard J H Smith8, Howard Trachtman2, Peter S Heeger9, Sanjay Ram10, Brad H Rovin7, Shadab Ali11, Nicole Arceneaux11, Isa Ashoor12, Laura Bailey-Wickins11, Jonathan Barratt13, Laurence Beck14, Daniel C Cattran15, Paolo Cravedi9, Elif Erkan16, Fernando Fervenza17, Ashley A Frazer-Abel18, Veronique Fremeaux-Bacchi19, Lindsey Fuller11, Rasheed Gbadegesin20, Jonathan J Hogan21, Krzysztof Kiryluk22, Moglie le Quintrec-Donnette23, Christoph Licht15, John D Mahan7, Matthew C Pickering24, Richard Quigg25, Michelle Rheault26, Pierre Ronco27, Minnie M Sarwal28, Christine Sethna29, Cathie Spino30, Mark Stegall17, Marina Vivarelli31, David L Feldman11, Joshua M Thurman18.
Abstract
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.Entities:
Keywords: Glomerular disease; clinical trial design; complement biomarkers; complement blockade; complement inhibition; complement-mediated glomerulopathy; drug approval pathway; drug safety; glomerulonephritides; infectious risk; patient-reported outcome (PRO); rare diseases; research priorities; surrogate outcome; trial end points
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Year: 2021 PMID: 34571062 DOI: 10.1053/j.ajkd.2021.07.025
Source DB: PubMed Journal: Am J Kidney Dis ISSN: 0272-6386 Impact factor: 8.860