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.

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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
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article

Utilization of Model‐Informed Drug Development in Early Clinical Development: Case Study of a Hb Modulator for Treatment of Sickle Cell Disease

Nessy Tania, Jatin Narula, Chay Ngee Lim, Steven Arkin et al.
CPT Pharmacometrics & Systems Pharmacology
Hemoglobinopathies and Related Disorders
article

Utilization of Model‐Informed Drug Development in Early Clinical Development: Case Study of a Hb Modulator for Treatment of Sickle Cell Disease

Nessy Tania, Jatin Narula, Chay Ngee Lim, Steven Arkin, Satyaprakash Nayak, Denis Rybin
article en

Abstract

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.

CPT Pharmacometrics & Systems PharmacologyVol. 15(4)
Pfizer (United States) (US)
Peace, Justice and strong institutions
Openalex Percentile: Top 3%
Hemoglobinopathies and Related Disorders
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