Impact of Model‐Informed Drug Development on Drug Development Cycle Times and Clinical Trial Cost
Model-informed drug development (MIDD) integrates data to quantify benefit/risk informing objective drug discovery and development decisions. An additional critical benefit of MIDD is postulated to be improvement in trial and program efficiencies. While the application of MIDD has grown, there have been no clear examples across programs to demonstrate its value at the portfolio level. This manuscript offers a methodology and examples to demonstrate MIDD value in terms of time and cost savings. We utilized an algorithm to estimate savings based on MIDD-related activities at each stage of development across the entire drug development portfolio during a typical year between 2021 and 2023. This algorithm, although company-specific, demonstrated general applicability across several programs of the portfolio. Overall, the use of MIDD yielded annualized average savings of approximately 10 months of cycle time and $5 million per program. Systematic application of MIDD approaches yielded significant time and cost savings across the drug development portfolio in addition to informing data-driven decisions. Increased utilization of MIDD approaches is a driver for improving drug development efficiency.
Authors
- Brian Corrigan (ORCID: https://orcid.org/0009-0007-0166-7076)
- Cynthia J. Musante (ORCID: https://orcid.org/0000-0002-3003-0169)
- Vaishali Sahasrabudhe (ORCID: https://orcid.org/0009-0007-2592-6490)
- Gianluca Nucci
- Timothy Nicholas
Institutions
- Pfizer (United States) (US)
- Metrum Research Group (United States) (US)
Publication Details
- Journal
- Clinical Pharmacology & Therapeutics
- Published
- 2025-03-26
- DOI
- https://doi.org/10.1002/cpt.3636
- Citations
- 15
- Primary Topic
- Health Systems, Economic Evaluations, Quality of Life
- Type
- article
- Field-Weighted Citation Impact
- 46.97