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
相关论文
共 55 条
  • [1] Triterpenoid CDDO-Me blocks the NF-κB pathway by direct inhibition of IKKβ on Cys-179
    Ahmad, Rehan
    Raina, Deepak
    Meyer, Colin
    Kharbanda, Surender
    Kufe, Donald
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (47) : 35764 - 35769
  • [2] The synthetic triterpenoid RTA dh404 (CDDO-dhTFEA) restores Nrf2 activity and attenuates oxidative stress, inflammation, and fibrosis in rats with chronic kidney disease
    Aminzadeh, Mohammad A.
    Reisman, Scott A.
    Vaziri, Nosratola D.
    Khazaeli, Mahyar
    Yuan, Jun
    Meyer, Colin J.
    [J]. XENOBIOTICA, 2014, 44 (06) : 570 - 578
  • [3] [Anonymous], ANN REP 2013
  • [4] [Anonymous], ANN REPORT
  • [5] Apfel Stuart C., 1999, American Journal of Medicine, V107, p34S
  • [6] Aleglitazar, a new, potent, and balanced dual PPARα/γ agonist for the treatment of type II diabetes
    Benardeau, Agnes
    Benz, Joerg
    Binggeli, Alfred
    Blum, Denise
    Boehringer, Markus
    Grether, Uwe
    Hilpert, Hans
    Kuhn, Bernd
    Maerki, Hans Peter
    Meyer, Markus
    Puentener, Kurt
    Raab, Susanne
    Ruf, Armin
    Schlatter, Daniel
    Mohr, Peter
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2009, 19 (09) : 2468 - 2473
  • [7] Alpha7 nicotinic receptors as novel therapeutic targets for inflammation-based diseases
    Bencherif, Merouane
    Lippiello, Patrick M.
    Lucas, Rudolf
    Marrero, Mario B.
    [J]. CELLULAR AND MOLECULAR LIFE SCIENCES, 2011, 68 (06) : 931 - 949
  • [8] Piragliatin (RO4389620), a Novel Glucokinase Activator, Lowers Plasma Glucose Both in the Postabsorptive State and after a Glucose Challenge in Patients with Type 2 Diabetes Mellitus: A Mechanistic Study
    Bonadonna, Riccardo C.
    Heise, Tim
    Arbet-Engels, Christophe
    Kapitza, Christoph
    Avogaro, Angelo
    Grimsby, Joe
    Zhi, Jay
    Grippo, Joseph F.
    Balena, Raffaella
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2010, 95 (11) : 5028 - 5036
  • [9] TAK-875 versus placebo or glimepiride in type 2 diabetes mellitus: a phase 2, randomised, double-blind, placebo-controlled trial
    Burant, Charles F.
    Viswanathan, Prabhakar
    Marcinak, John
    Cao, Charlie
    Vakilynejad, Majid
    Xie, Benhuai
    Leifke, Eckhard
    [J]. LANCET, 2012, 379 (9824) : 1403 - 1411
  • [10] Reversibility of established diabetic glomerulopathy by anti-TGF-β antibodies in dbldb mice
    Chen, S
    Igleasias-de la Cruz, MC
    Jim, B
    Hong, SW
    Isono, M
    Ziyadeh, FN
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 300 (01) : 16 - 22