Pharmacokinetic Modeling of Bepotastine for Determination of Optimal Dosage Regimen in Pediatric Patients with Allergic Rhinitis or Urticaria

Author:

Yoon Sukyong1ORCID,Jin Byung Hak23ORCID,Kim Choon Ok23ORCID,Park Kyungsoo1ORCID,Park Min Soo34ORCID,Chae Dongwoo1

Affiliation:

1. Department of Pharmacology, Yonsei University College of Medicine, Seoul 03722, Republic of Korea

2. Clinical Trials Center, Severance Hospital, Yonsei University College of Medicine, Seoul 03722, Republic of Korea

3. Department of Clinical Pharmacology, Severance Hospital, Yonsei University College of Medicine, Seoul 03722, Republic of Korea

4. Department of Pediatrics, Yonsei University College of Medicine, Seoul 03722, Republic of Korea

Abstract

Bepotastine, a second-generation antihistamine for allergic rhinitis and urticaria, is widely used in all age groups but lacks appropriate dosing guidelines for pediatric patients, leading to off-label prescriptions. We conducted this study to propose an optimal dosing regimen for pediatric patients based on population pharmacokinetic (popPK) and physiologically based pharmacokinetic (PBPK) models using data from two previous trials. A popPK model was built using NONMEM software. A one-compartment model with first-order absorption and absorption lag time described our data well, with body weight incorporated as the only covariate. A PBPK model was developed using PK-Sim software version 10, and the model well predicted the drug concentrations obtained from pediatric patients. Furthermore, the final PBPK model showed good concordance with the known properties of bepotastine. Appropriate pediatric doses for different weight and age groups were proposed based on the simulations. Discrepancies in recommended doses from the two models were likely due to the incorporation of age-dependent physiological factors in the PBPK model. In conclusion, our study is the first to suggest an optimal oral dosing regimen of bepotastine in pediatric patients using both approaches. This is expected to foster safer and more productive use of the drug.

Funder

Ministry of Food and Drug Safety

Kolon Pharmaceuticals

Publisher

MDPI AG

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