In Silico Hypothesis Testing in Drug Discovery: Using Quantitative Systems Pharmacology Modeling to Evaluate the Therapeutic Value of Proinsulin Conversion to Insulin Therapy for Type 2 Diabetes Mellitus
<b>Background/Objectives</b>: Proinsulin, the precursor to insulin, has limited activity on the insulin receptor. Proinsulin levels increase with increasing insulin resistance in type 2 diabetes due to incomplete processing by the β-cell. To assess whether the development of peptides that could convert circulating proinsulin to insulin in the blood would provide therapeutic value, we used a quantitative systems pharmacology (QSP) model of glucose homeostasis. In silico hypothesis testing such as this is an example of how modeling can inform decisions in drug discovery. <b>Methods</b>: In silico hypothesis testing involved (1) the addition and qualification of proinsulin biology into a preexisting QSP model, (2) the creation and validation of virtual patients (VPs) for subpopulations of type 2 diabetics based on phenotypic traits, and (3) the simulation of clinical trials evaluating the therapeutic value of the conversion of circulating proinsulin to insulin in the VPs created. <b>Results</b>: Proinsulin conversion led to a ~0.2% reduction in HbA1c in VPs at varying stages of diabetes, a decrease that does not hold meaningful therapeutic value. The lack of significant impact on HbA1c was likely a result of the surprisingly small effect on plasma insulin levels from proinsulin, which has a significantly slower secretion and clearance rate. Although patients with higher proinsulin/insulin ratios showed the largest reductions, clinically significant ≥ 0.5% reduction in HbA1c required ratios of proinsulin/insulin above the reported physiological range. <b>Conclusions</b>: This effort demonstrates how in silico hypothesis testing using QSP modeling can provide insights on the probability of success of novel interventions with minimal time and resources. These efficiencies are a means of overcoming the pressures on the pharmaceutical industry to do more with less in providing therapies that improve the lives of patients.
Authors
- Paul E. Carrington
- Maria E. Trujillo (ORCID: https://orcid.org/0000-0002-9358-5532)
- Steven C. Hayes (ORCID: https://orcid.org/0000-0003-4399-6859)
- Rebecca Baillie (ORCID: https://orcid.org/0000-0003-3966-6320)
- Mike Reed (ORCID: https://orcid.org/0000-0002-6309-2710)
- Douglas Chung (ORCID: https://orcid.org/0009-0009-4243-234X)
- Yue Han (ORCID: https://orcid.org/0000-0001-7372-6724)
- Michael Weis
Institutions
- Merck & Co., Inc., Rahway, NJ, USA (United States) (US)
- Rosa (United States) (US)
Publication Details
- Journal
- Pharmaceutics
- Published
- 2025-11-26
- DOI
- https://doi.org/10.3390/pharmaceutics17121522
- Primary Topic
- Diabetes Management and Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00