Utilization of Model‐Informed Drug Development in Early Clinical Development: Case Study of a Hb Modulator for Treatment of Sickle Cell Disease
Model-informed drug development (MIDD) has an important role to play at various stages of drug development. In this case study, the application of MIDD in the early clinical development of a small-molecule inhibitor of sickle hemoglobin (Hb) polymerization is highlighted. Starting from the setting of quantitative criteria, to using a combination of PKPD and semi-mechanistic RBC modeling, and key biomarker analysis, based on data from a healthy participant first-in-human (FIH) study and historical data, we chart the strategic approaches planned and taken to inform decisions for the program, and the role of cross-functional collaboration. Based on the projections from the PKPD and semi-mechanistic RBC models, and key biomarker results from healthy participants, an informed decision was made to not proceed to a Phase 1b study in sickle cell disease (SCD) patients, underscoring the value of MIDD in early drug development decision making.
Authors
- Nessy Tania (ORCID: https://orcid.org/0000-0003-4256-2434)
- Jatin Narula (ORCID: https://orcid.org/0000-0002-2458-2055)
- Chay Ngee Lim (ORCID: https://orcid.org/0000-0002-7307-9851)
- Steven Arkin (ORCID: https://orcid.org/0000-0001-6922-4246)
- Satyaprakash Nayak
- Denis Rybin
Institutions
- Pfizer (United States) (US)
Publication Details
- Journal
- CPT Pharmacometrics & Systems Pharmacology
- Published
- 2026-03-27
- DOI
- https://doi.org/10.1002/psp4.70238
- Primary Topic
- Hemoglobinopathies and Related Disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.00