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
. 2015 Aug;47(8):856-60.
doi: 10.1038/ng.3314. Epub 2015 Jun 29.

The support of human genetic evidence for approved drug indications

Affiliations

The support of human genetic evidence for approved drug indications

Matthew R Nelson et al. Nat Genet. 2015 Aug.

Abstract

Over a quarter of drugs that enter clinical development fail because they are ineffective. Growing insight into genes that influence human disease may affect how drug targets and indications are selected. However, there is little guidance about how much weight should be given to genetic evidence in making these key decisions. To answer this question, we investigated how well the current archive of genetic evidence predicts drug mechanisms. We found that, among well-studied indications, the proportion of drug mechanisms with direct genetic support increases significantly across the drug development pipeline, from 2.0% at the preclinical stage to 8.2% among mechanisms for approved drugs, and varies dramatically among disease areas. We estimate that selecting genetically supported targets could double the success rate in clinical development. Therefore, using the growing wealth of human genetic data to select the best targets and indications should have a measurable impact on the successful development of new drugs.

PubMed Disclaimer

Comment in

Similar articles

Cited by

References

    1. Drug Discov Today. 2012 May;17(9-10):419-24 - PubMed
    1. PLoS Genet. 2013;9(8):e1003709 - PubMed
    1. Nucleic Acids Res. 2012 Jan;40(Database issue):D1047-54 - PubMed
    1. Nat Rev Drug Discov. 2013 Aug;12(8):569 - PubMed
    1. AMIA Annu Symp Proc. 2009 Nov 14;2009:431-5 - PubMed

Publication types

MeSH terms