Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2012 Apr;53(4):478, 480-5, 487.
doi: 10.1007/s00108-012-3014-9.

[Benefits and risks of current pharmacotherapy in the treatment of type 2 diabetes]

[Article in German]
Affiliations

[Benefits and risks of current pharmacotherapy in the treatment of type 2 diabetes]

[Article in German]
C Schindler et al. Internist (Berl). 2012 Apr.

Abstract

The development of new drugs for the treatment of type 2 diabetes (T2DM) and metabolic disorders is currently one of the most innovative areas of drug development. However, a considerable number of newly developed drugs have either not reached the market and were stopped late in development or have been withdrawn after initial approval soon after market authorization due to serious safety concerns. How can drug safety problems be anticipated and, even more important, how can adverse events definitely caused by a drug be differentiated from incidences of naturally occurring diseases? This review article will provide an update about the state of the art treatment of type 2 diabetes and reflect on the newest available study evidence on glitazones, incretin mimetics (GLP-1 agonists and DPP-4 inhibitors), SGLT-2 inhibitors (gliflocines) and pan-PPAR agonists (glitazars). Furthermore, new and still experimental approaches for the treatment of T2DM, such as bardoxolone, salsalate and anakinra will be briefly reviewed.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Lab Invest. 2009 May;89(5):489-97 - PubMed
    1. Int J Clin Pract. 2010 Jun;64(7):984-90 - PubMed
    1. Am J Physiol Endocrinol Metab. 2010 Dec;299(6):E1076-86 - PubMed
    1. Diabetes Res Clin Pract. 2011 Jul;93(1):49-55 - PubMed
    1. Diabetes Obes Metab. 2010 Jun;12(6):495-509 - PubMed

Publication types

MeSH terms

Substances

LinkOut - more resources