Proposed study designs for approval based on a surrogate endpoint and a post-marketing confirmatory study under FDA's accelerated approval regulations for disease modifying osteoarthritis drugs
Virginia B. Kraus(Duke University), Lee S. Simon, Jeffrey N. Katz(Brigham and Women's Hospital), Tuhina Neogi(Boston University), David J. Hunter(The University of Sydney), A. Guermazi(Boston University), M.A. Karsdal(Nordic Bioscience (Denmark))
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