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Updated: Jan 9, 2026

A Semi-Quantitative Drug Affinity Responsive Target Stability DARTS assay for studying Rapamycin/mTOR interaction
Published on: August 27, 2019
Temporal trends in evidence supporting novel drug target discovery
Maria J Falaguera1,2, Ellen M McDonagh3,4,5, David Ochoa3,4
1Open Targets, Wellcome Genome Campus, Hinxton, UK. mariaf@ebi.ac.uk.
None:
Over the past decade, about one-fifth of FDA-approved drugs each year involve novel mechanism-of-action human targets. Although riskier than modulating well-known targets, these therapies address unmet needs and strengthen sector innovation. The Open Targets Platform is a valuable open resource for identifying novel targets, integrating diverse datasets with regular updates and a user-friendly interface. To expand its capabilities, we implement comprehensive timestamping across millions of biomedical data points and introduce a target novelty metric for disease contexts, enabling discovery of novel targets within the ecosystem. We also present a retrospective analysis of novel drug target approvals over two decades, revealing a shift around 2015: supportive biomedical evidence (e.g., human genetics, literature-derived insights, differential expression, and pathway data) increasingly appears before rather than after the approval year. These findings underscore the importance of time-based evidence assessments for earlier identification of novel clinical opportunities and offer guidance for future target selection trends.
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