Abstract
Long acting injectables (LAI) products are a popular intervention for treating a number of chronic conditions,
with their long drug release reducing the administration frequency and thus improving patient adherence.
The extended release, however, can provide a major challenge to bioequivalence (BE) testing since the long absorption half-life results in a long washout period, meaning that a traditional BE study can be many months or years in length. The unique PK profile for LAI products also means that it is critical to have
appropriate metrics to summarise the plasma concentration profile. In this work, we use paliperidone as a
case study to demonstrate how Population PK modelling can be utilised to explore sensitivity of summary
metrics to different products. We also determine a range of products that are bioequivalent after both
multiple dosing and single dosing. Finally, we show how the modelling can be used in a (virtual) PK
study as an alternative approach to determining bioequivalence. This work demonstrates the potential
for Population PK modelling in bioequivalence assessment, opening doors to more streamlined product
development.
with their long drug release reducing the administration frequency and thus improving patient adherence.
The extended release, however, can provide a major challenge to bioequivalence (BE) testing since the long absorption half-life results in a long washout period, meaning that a traditional BE study can be many months or years in length. The unique PK profile for LAI products also means that it is critical to have
appropriate metrics to summarise the plasma concentration profile. In this work, we use paliperidone as a
case study to demonstrate how Population PK modelling can be utilised to explore sensitivity of summary
metrics to different products. We also determine a range of products that are bioequivalent after both
multiple dosing and single dosing. Finally, we show how the modelling can be used in a (virtual) PK
study as an alternative approach to determining bioequivalence. This work demonstrates the potential
for Population PK modelling in bioequivalence assessment, opening doors to more streamlined product
development.
Original language | English |
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Pages (from-to) | 106296 |
Journal | European Journal of Pharmaceutical Sciences |
Volume | 179 |
Early online date | 20 Sept 2022 |
DOIs | |
Publication status | Published - 1 Dec 2022 |