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.

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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
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article

Impact of Model‐Informed Drug Development on Drug Development Cycle Times and Clinical Trial Cost

Brian Corrigan, Cynthia J. Musante, Vaishali Sahasrabudhe, Gianluca Nucci et al.
15 citations
Clinical Pharmacology & Therapeutics
Health Systems, Economic Evaluations, Quality of Life
46.97
article

Impact of Model‐Informed Drug Development on Drug Development Cycle Times and Clinical Trial Cost

Brian Corrigan, Cynthia J. Musante, Vaishali Sahasrabudhe, Gianluca Nucci, Timothy Nicholas
article en
15 citations

Abstract

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.

Clinical Pharmacology & TherapeuticsVol. 118(2)
Pfizer (United States) (US), Metrum Research Group (United States) (US)
Openalex Percentile: Top 0%
Health Systems, Economic Evaluations, Quality of Life
46.97
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Impact of Model‐Informed Drug Development on Drug Development Cycle Times and Clinical Trial Cost — Brian Corrigan, Cynthia J. Musante, et al. · Clinical Pharmacology & Therapeutics (2025) | TGRS Research Map | TGRS