Using All Longitudinal Data to Define Time to Specified Percentages of Estimated GFR Decline: A Simulation Study
Author:
Funder
NEPTUNE Consortium
NIH
Publisher
Elsevier BV
Subject
Nephrology
Reference11 articles.
1. Surrogate end points for clinical trials of kidney disease progression;Stevens;Clin J Am Soc Nephrol,2006
2. GFR decline as an end point of clinical trials in CKD: a scientific workshop sponsored by the National Kidney Foundation and the US Food and Drug Administration;Levey;Am J Kidney Dis,2014
3. GFR decline as an end point in trials of CKD: a viewpoint from the FDA;Thompson;Am J Kidney Dis,2014
4. Surrogate outcomes for ESRD risk: the case for a 30% reduction in estimated GFR over 2 years;Sontrop;Am J Kidney Dis,2014
5. Utility and validity of estimated GFR-based surrogate time-to-event end points in CKD: a simulation study;Greene;Am J Kidney Dis,2014
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