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Trial watch: phase II and phase III attrition rates 2011-2012.

John Arrowsmith, +1 more
- 01 Aug 2013 - 
- Vol. 12, Iss: 8, pp 569-569
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This article is published in Nature Reviews Drug Discovery.The article was published on 2013-08-01 and is currently open access. It has received 549 citations till now. The article focuses on the topics: MEDLINE.

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The ChEMBL database in 2017.

TL;DR: ChEMBL is an open large-scale bioactivity database that includes the annotation of assays and targets using ontologies, the inclusion of targets and indications for clinical candidates, addition of metabolic pathways for drugs and calculation of structural alerts.
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High-throughput screening using patient-derived tumor xenografts to predict clinical trial drug response

TL;DR: The results suggest that PCTs may represent a more accurate approach than cell line models for assessing the clinical potential of some therapeutic modalities and could potentially improve preclinical evaluation of treatmentmodalities and enhance the ability to predict clinical trial responses.
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The support of human genetic evidence for approved drug indications

TL;DR: It is estimated that selecting genetically supported targets could double the success rate in clinical development, and 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.
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Lessons learned from the fate of AstraZeneca's drug pipeline: a five-dimensional framework

TL;DR: A comprehensive longitudinal review of AstraZeneca's small-molecule drug projects from 2005 to 2010 allowed us to establish a framework based on the five most important technical determinants of project success and pipeline quality, which are described as the five 'R's'.
Journal ArticleDOI

Three-Dimensional in Vitro Cell Culture Models in Drug Discovery and Drug Repositioning.

TL;DR: Common approaches to 3D culture are reviewed, the significance of 3D cultures in drug resistance and drug repositioning is discussed and some of the challenges of applying 3D cell cultures to high-throughput drug discovery are addressed.
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