Discontinued in 2013: diabetic drugs

被引:24
|
作者
Hedrington, Maka S. [1 ,2 ]
Davis, Stephen N. [3 ]
机构
[1] Univ Maryland, Sch Med, Baltimore, MD 21201 USA
[2] Univ Maryland, Dept Med, Baltimore, MD 21201 USA
[3] Univ Maryland, Sch Med, Dept Med, Baltimore, MD 21201 USA
关键词
aleglitazar; diabetes; diabetic nephropathy; discontinued drugs; fasiglifam; GLUCOSE COTRANSPORTER 2; ADVERSE CARDIOVASCULAR EVENTS; PPAR-ALPHA/GAMMA AGONIST; GROWTH-FACTOR NGF; DOUBLE-BLIND; GLUCOKINASE ACTIVATOR; GPR40; AGONIST; IPRAGLIFLOZIN ASP1941; NEUROTROPHIC FACTOR; BARDOXOLONE METHYL;
D O I
10.1517/13543784.2014.964859
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: The increasing prevalence of diabetes, with no cure on the horizon, continues to provide biopharmaceutical companies with an incentive to develop novel therapies and improve existing compounds. Areas covered: The following paper provides a summary of the experimental drug projects targeted for diabetes and associated complications that were discontinued in 2013. The discontinued projects, highlighted in this article, were identified via biopharmaceutical company pipelines, annual reports, and press releases. The authors also used other sources including: Google, ClinicalTrials.gov, and PubMed. Compounds were in various stages of development at termination and many of them had been associated with favorable effects in earlier studies. Expert opinion: There were two main reasons for the termination of antidiabetic compounds that dominated 2013: concerns about safety and efficacy. Attempts to discover a novel mechanism that is both safe and effective in human disease present many challenges, not least is the cost for developing new treatments.
引用
收藏
页码:1703 / 1711
页数:9
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