New medications in development for the treatment of hyperuricemia of gout

被引:120
作者
Diaz-Torne, Cesar [1 ]
Perez-Herrero, Nuria [2 ]
Perez-Ruiz, Fernando [3 ,4 ]
机构
[1] Hosp Santa Creu & Sant Pau, Div Rheumatol, Barcelona, Spain
[2] Univ Rey Juan Carlos, Biomed Sci Sch, Madrid, Spain
[3] Hosp Univ Cruces, Div Rheumatol, Baracaldo 48903, Vizcaya, Spain
[4] BioCruces Hlth Res Inst, Baracaldo 48903, Vizcaya, Spain
关键词
arhalofenate; gout; gout suppressants; lesinurad; ulodesine; uric acid; URIC-ACID; URATE; PEGLOTICASE; MANAGEMENT; INHIBITOR; LESINURAD; EFFICACY; ANTIBODY; DISEASE;
D O I
10.1097/BOR.0000000000000146
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Purpose of review To update recent developments in medications targeting hyperuricemia, but not including medications recently labelled in the European Union and the United States. Recent findings A new xanthine oxidase inhibitor, Topiloric (Fujiyakuhin Co., Ltd. Japan) Uriadec (Sanwa Kagaku Kenkyusho Co., Ltd. Japan), has been developed and labelled in Japan. An inhibitor of purine nucleoside phosphorylase, Ulodesine, is in development in combination with allopurinol. The rest of the medications in the pipeline for hyperuricemia are targeting renal transporters of uric acid, mainly URAT1 and OAT4, acting as uricosuric agents. Most of them, such as lesinurad and arhalofenate, are being tested in trials in combination with allopurinol and febuxostat. The most potent RDEA3170 is being tested in monotherapy, but also associated with febuxostat. Recently, medications showing dual activity, inhibiting both xanthine oxidoreductase and URAT1, have been communicated or started exploratory clinical trials. There is no report of medications targeting other transporters such as Glut9 or ABCG2. Summary There are a number of medications in the pipeline targeting hyperuricemia, mostly uricosurics in combination with xanthine oxidase inhibitors, but some targeting both xanthine oxidoreductase and URAT1. Increasing the number of available medications will ensure proper control of hyperuricemia to target serum urate levels in the near future for most, if not all, patients with hyperuricemia.
引用
收藏
页码:164 / 169
页数:6
相关论文
共 40 条
[1]
Ahn SO, 2013, ANN RHEUM DIS, V72, P704
[2]
[Anonymous], 2014, RDEA3170
[3]
Plasma urate level is directly regulated by a voltage-driven urate efflux transporter URATv1 (SLC2A9) in humans [J].
Anzai, Naohiko ;
Ichida, Kimiyoshi ;
Jutabha, Promsuk ;
Kimura, Toru ;
Babu, Ellappan ;
Jin, Chun Ji ;
Srivastava, Sunena ;
Kitamura, Kenichiro ;
Hisatome, Ichiro ;
Endou, Hitoshi ;
Sakurai, Hiroyuki .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2008, 283 (40) :26834-26838
[4]
Recent advances in renal urate transport: characterization of candidate transporters indicated by genome-wide association studies [J].
Anzai, Naohiko ;
Jutabha, Promsuk ;
Amonpatumrat-Takahashi, Sirirat ;
Sakurai, Hiroyuki .
CLINICAL AND EXPERIMENTAL NEPHROLOGY, 2012, 16 (01) :89-95
[5]
BASSETT DR, 1977, CLIN PHARMACOL THER, V22, P340
[6]
Becker MA, 2012, ANN RHEUM DIS S3, V71, P348
[7]
Choi YJ, 2012, ARTHRITIS RHEUM-US, V64, pS697
[8]
A systematic review of ultrasonography in gout and asymptomatic hyperuricaemia [J].
Chowalloor, Priya V. ;
Keen, Helen Isobel .
ANNALS OF THE RHEUMATIC DISEASES, 2013, 72 (05) :638-645
[9]
Clinical Trials gov, 2014, KUX1151
[10]
Clinical Trials gov, 2014, ARH