Drug Repositioning by Mining Adverse Event Data in ClinicalTrials.gov

3Citations
Citations of this article
14Readers
Mendeley users who have this article in their library.
Get full text

Abstract

The protocol below describes an in silico method for drug repositioning (drug repurposing). The data source is ClinicalTrials.gov, which contains about a quarter of a million clinical studies. Mining such rich and clean clinical summary data could be helpful to many health-related researches. Described here is a method that utilizes serious adverse event data to identify potential new uses of drugs and dietary supplements (repositioning).

Cite

CITATION STYLE

APA

Su, E. W. (2019). Drug Repositioning by Mining Adverse Event Data in ClinicalTrials.gov. In Methods in Molecular Biology (Vol. 1903, pp. 61–72). Humana Press Inc. https://doi.org/10.1007/978-1-4939-8955-3_4

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free