Emerging drugs for chronic kidney disease

被引:10
|
作者
Stefoni, Sergio [1 ]
Cianciolo, Giuseppe [1 ]
Baraldi, Olga [1 ]
Iorio, Mario [1 ]
Angelini, Maria Laura [1 ]
机构
[1] S Orsola Univ Hosp, Dept Expt Diagnost & Special Med, Dialysis Nephrol & Trasplantat Unit, I-40138 Bologna, Italy
关键词
albuminuria; bardoxolone; chronic kidney disease; end stage renal disease; endothelin receptor antagonist; paricalcitol; renin-angiotensin-aldosterone system; STAGE RENAL-DISEASE; ANGIOTENSIN-ALDOSTERONE SYSTEM; CONVERTING ENZYME-INHIBITION; DEPENDENT DIABETIC-PATIENTS; EARLY EVALUATION PROGRAM; HIGH VASCULAR RISK; VITAMIN-D; BARDOXOLONE METHYL; HEART-FAILURE; UNITED-STATES;
D O I
10.1517/14728214.2014.900044
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Chronic kidney disease (CKD) is a worldwide health problem. Despite remarkable headway in slowing the progression of kidney diseases, the incidence of end-stage renal disease (ESRD) is increasing in all countries with a severe impact on patients and society. The high incidence of diabetes and hypertension, along with the aging population, may partially explain this growth. Currently, the mainstay of pharmacological treatment for CKD, aiming to slow progression to ESRD are ACE inhibitors and angiotensin II receptor blockers for their hemodynamic/antihypertensive and anti-inflammatory/antifibrotic action. However, novel drugs would be highly desirable to effectively slow the progressive renal function loss. Areas covered: Through the search engines, PubMed and ClinicalTrial.gov, the scientific literature was reviewed in search of emerging drugs in Phase II or III trials, which appear to be the most promising for CKD treatment. Expert opinion: The great expectations for new drugs for the management of CKD over the last decade have unfortunately not been met. Encouraging results from preliminary studies with specific agents need to be tempered with caution, given the absence of consistent and adequate data. To date, several agents that showed great promise in animal studies have been less effective in humans.
引用
收藏
页码:183 / 199
页数:17
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