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
  • [41] Bardoxolone Methyl and Kidney Function in CKD with Type 2 Diabetes
    Pergola, Pablo E.
    Raskin, Philip
    Toto, Robert D.
    Meyer, Colin J.
    Huff, J. Warren
    Grossman, Eric B.
    Krauth, Melissa
    Ruiz, Stacey
    Audhya, Paul
    Christ-Schmidt, Heidi
    Wittes, Janet
    Warnock, David G.
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2011, 365 (04) : 327 - 336
  • [42] Transforming growth factor β contributes to progressive diabetic nephropathy
    Reeves, WB
    Andreoli, TE
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (14) : 7667 - 7669
  • [43] Antioxidants in Kidney Diseases: The Impact of Bardoxolone Methyl
    Rojas-Rivera, Jorge
    Ortiz, Alberto
    Egido, Jesus
    [J]. INTERNATIONAL JOURNAL OF NEPHROLOGY, 2012, 2012
  • [44] Safety issues and prospects for future generations of PPAR modulators
    Rubenstrunk, Anne
    Hanf, Remy
    Hum, Dean W.
    Fruchart, Jean-Charles
    Staels, Bart
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 2007, 1771 (08): : 1065 - 1081
  • [45] Pharmacokinetics, Pharmacodynamics, and Tolerability of Aleglitazar in Patients With Type 2 Diabetes: Results From a Randomized, Placebo-Controlled Clinical Study
    Sanwald-Ducray, P.
    D'ardhuy, X. Liogier
    Jamois, C.
    Banken, L.
    [J]. CLINICAL PHARMACOLOGY & THERAPEUTICS, 2010, 88 (02) : 197 - 203
  • [46] Discovery of Piragliatin-First Glucokinase Activator Studied in Type 2 Diabetic Patients
    Sarabu, Ramakanth
    Bizzarro, Fred T.
    Corbett, Wendy L.
    Dvorozniak, Mark T.
    Geng, Wanping
    Grippo, Joseph F.
    Haynes, Nancy-Ellen
    Hutchings, Stanley
    Garofalo, Lisa
    Guertin, Kevin R.
    Hilliard, Darryl W.
    Kabat, Marek
    Kester, Robert F.
    Ka, Wang
    Liang, Zhenmin
    Mahaney, Paige E.
    Marcus, Linda
    Matschinsky, Franz M.
    Moore, David
    Racha, Jagdish
    Radinov, Roumen
    Ren, Yi
    Qi, Lida
    Pignatello, Michael
    Spence, Cheryl L.
    Steele, Thomas
    Tengi, John
    Grimsby, Joseph
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 2012, 55 (16) : 7021 - 7036
  • [47] Safety, Pharmacokinetic, and Pharmacodynamic Profiles of Ipragliflozin (ASP1941), a Novel and Selective Inhibitor of Sodium-Dependent Glucose Co-Transporter 2, in Patients with Type 2 Diabetes Mellitus
    Schwartz, Sherwyn L.
    Akinlade, Bola
    Klasen, Sally
    Kowalski, Donna
    Zhang, Wenhui
    Wilpshaar, Wim
    [J]. DIABETES TECHNOLOGY & THERAPEUTICS, 2011, 13 (12) : 1219 - 1227
  • [48] Neutralization of TGF-beta by anti-TGF-beta antibody attenuates kidney hypertrophy and the enhanced extracellular matrix gene expression in STZ-induced diabetic mice
    Sharma, K
    Jin, YL
    Guo, J
    Ziyadeh, FN
    [J]. DIABETES, 1996, 45 (04) : 522 - 530
  • [49] Therapeutic roles of peroxisome proliferator-activated receptor agonists
    Staels, B
    Fruchart, JC
    [J]. DIABETES, 2005, 54 (08) : 2460 - 2470
  • [50] TAK-875, an Orally Available G Protein-Coupled Receptor 40/Free Fatty Acid Receptor 1 Agonist, Enhances Glucose-Dependent Insulin Secretion and Improves Both Postprandial and Fasting Hyperglycemia in Type 2 Diabetic Rats
    Tsujihata, Yoshiyuki
    Ito, Ryo
    Suzuki, Masami
    Harada, Ayako
    Negoro, Nobuyuki
    Yasuma, Tsuneo
    Momose, Yu
    Takeuchi, Koji
    [J]. JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2011, 339 (01) : 228 - 237