Developing Treatments for Chronic Kidney Disease in the 21st Century

被引:55
作者
Breyer, Matthew D. [1 ]
Susztak, Katalin [2 ]
机构
[1] Eli Lilly & Co, Biotechnol Discovery Res, Indianapolis, IN 46285 USA
[2] Univ Penn, Dept Med, Renal Electrolyte & Hypertens Div, Philadelphia, PA 19104 USA
关键词
Diabetic nephropathy; SGTL2; Angiotensin; inflammation; renal outcomes; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; VASCULAR ADHESION PROTEIN-1; TYPE-2; DIABETES-MELLITUS; MONOCYTE CHEMOATTRACTANT PROTEIN-1; COMPLEMENT INHIBITOR ECULIZUMAB; SHARED TRANSCRIPTIONAL NETWORKS; APPROPRIATE THERAPEUTIC TARGET; POST-HOC ANALYSIS; BLOOD-PRESSURE; END-POINTS;
D O I
10.1016/j.semnephrol.2016.08.001
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Chronic kidney disease (CKD) is a lethal and rapidly increasing burden on society. Despite this, there are relatively few therapies in development for the treatment of CKD. Several recent costly phase 3 trials have failed to provide improved renal outcomes, diminishing interest in pharmaceutical investment. Furthermore, poor patient, physician, and payer awareness of CKD as a diagnosis has contributed to slow trial enrollment and successful implementation of these trials. Nevertheless, several therapeutics remain in development for the treatment of CKD, including mineralocorticoid-receptor antagonists, sodium/glucose cotransporter 2 inhibitors, anti-inflammatory drugs, and drugs that mitigate oxidative injury. Success of future CKD therapeutic trials will depend not only on improved understanding of disease pathogenesis, but also on improved trial enrollment rates, through increasing awareness of this disease by the public, policy makers, and the greater medical community. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:436 / 447
页数:12
相关论文
共 144 条
[1]  
AbbVie, 2015, STUD DIAB NEPHR ATR
[2]   Mouse podocyte complement factor H: The functional analog to human complement receptor 1 [J].
Alexander, Jessy J. ;
Wang, Ying ;
Chang, Anthony ;
Jacob, Alexander ;
Minto, Andrew W. M. ;
Karmegam, Menaka ;
Haas, Mark ;
Quigg, Richard J. .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2007, 18 (04) :1157-1166
[3]   Comparative effects of non-steroidal anti-inflammatory drugs (NSAIDs) on blood pressure in patients with hypertension [J].
Aljadhey, Hisham ;
Tu, Wanzhu ;
Hansen, Richard A. ;
Blalock, Susan J. ;
Brater, D. Craig ;
Murray, Michael D. .
BMC CARDIOVASCULAR DISORDERS, 2012, 12
[4]  
Astellas, STUD EV ASP8232 ADD
[5]   Monocyte/macrophage chemokine receptor CCR2 mediates diabetic renal injury [J].
Awad, Alaa S. ;
Kinsey, Gilbert R. ;
Khutsishvili, Konstantine ;
Gao, Ting ;
Bolton, W. Kline ;
Okusa, Mark D. .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2011, 301 (06) :F1358-F1366
[6]   Effect of Finerenone on Albuminuria in Patients With Diabetic Nephropathy A Randomized Clinical Trial [J].
Bakris, George L. ;
Agarwal, Rajiv ;
Chan, Juliana C. ;
Cooper, Mark E. ;
Gansevoort, Ron T. ;
Haller, Hermann ;
Remuzzi, Giuseppe ;
Rossing, Peter ;
Schmieder, Roland E. ;
Nowack, Christina ;
Kolkhof, Peter ;
Joseph, Amer ;
Pieper, Alexander ;
Kimmeskamp-Kirschbaum, Nina ;
Ruilope, Luis M. .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2015, 314 (09) :884-894
[7]  
Bancroft D., 2015, NOX INHIBITOR CANDID
[8]   Angiotensin II blockade prevents hyperglycemia-induced activation of JAK and STAT proteins in diabetic rat kidney glomeruli [J].
Banes, AK ;
Shaw, S ;
Jenkins, J ;
Redd, H ;
Amiri, F ;
Pollock, DM ;
Marrero, MB .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2004, 286 (04) :F653-F659
[9]   Efficacy and safety of empagliflozin added to existing antidiabetes treatment in patients with type 2 diabetes and chronic kidney disease: a randomised, double-blind, placebo-controlled trial [J].
Barnett, Anthony H. ;
Mithal, Ambrish ;
Manassie, Jenny ;
Jones, Russell ;
Rattunde, Henning ;
Woerle, Hans J. ;
Broedl, Uli C. .
LANCET DIABETES & ENDOCRINOLOGY, 2014, 2 (05) :369-384
[10]  
Bayer, 2016, EFF SAF FIN SUBJ TYP