Benchmarking R&D success rates of leading pharmaceutical companies: an empirical analysis of FDA approvals (2006-2022)
- PMID: 39805539
- DOI: 10.1016/j.drudis.2025.104291
Benchmarking R&D success rates of leading pharmaceutical companies: an empirical analysis of FDA approvals (2006-2022)
Erratum in
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Corrigendum to "Benchmarking R&D success rates of leading pharmaceutical companies: an empirical analysis of FDA approvals (2006-2022)" [Drug Discov. Today 30(2) (2025) 104291].Drug Discov Today. 2025 May;30(5):104326. doi: 10.1016/j.drudis.2025.104326. Epub 2025 Mar 15. Drug Discov Today. 2025. PMID: 40081820 No abstract available.
Abstract
Previous analyses provide an industry benchmark of ∼10% for the success rate in clinical development. However, prior analyses were limited by a narrow timeframe, a diverse research focus, biases in phase-to-phase transition methodology or a focus on specific use cases. We calculated unbiased input:output ratios (Phase I to FDA new drug approval) to analyze the likelihood of first approval using data from clinicaltrials.gov, encompassing a total of 2092 active ingredients, 19 927 clinical trials conducted by 18 leading pharmaceutical companies (2006-2022) and 274 new drug approvals. Our study reveals an average likelihood of first approval rate of 14.3% across leading research-based pharmaceutical companies, broadly ranging from 8% to 23%.
Keywords: Pharma; R&D; R&D productivity; clinical development; clinical trials; drug development; likelihood of approval; success rate.
Copyright © 2025 The Author(s). Published by Elsevier Ltd.. All rights reserved.
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