Drug development for the treatment of onchocerciasis: population pharmacokinetic and adverse events modeling of emodepside
<p><strong>Background</strong><br> To accelerate the progress towards onchocerciasis elimination, a macrofilaricidal drug that kills the adult parasite is urgently needed. Emodepside has shown macrofilaricidal activity against a variety of nematodes and is currently under cli...
| 主要な著者: | , , , , , |
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| フォーマット: | Journal article |
| 言語: | English |
| 出版事項: |
Public Library of Science
2022
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| _version_ | 1826309751228596224 |
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| author | Assmus, F Hoglund, RM Monnot, F Specht, S Scandale, I Tarning, J |
| author_facet | Assmus, F Hoglund, RM Monnot, F Specht, S Scandale, I Tarning, J |
| author_sort | Assmus, F |
| collection | OXFORD |
| description | <p><strong>Background</strong><br>
To accelerate the progress towards onchocerciasis elimination, a macrofilaricidal drug that kills the adult parasite is urgently needed. Emodepside has shown macrofilaricidal activity against a variety of nematodes and is currently under clinical development for the treatment of onchocerciasis. The aims of this study were i) to characterize the population pharmacokinetic properties of emodepside, ii) to link its exposure to adverse events in healthy volunteers, and iii) to propose an optimized dosing regimen for a planned phase II study in onchocerciasis patients.<br><br>
<strong>Methodology / Principal findings</strong><br>
Plasma concentration-time profiles and adverse event data were obtained from 142 subjects enrolled in three phase I studies, including a single-dose, and a multiple-dose, dose-escalation study as well as a relative bioavailability study. Nonlinear mixed-effects modeling was used to evaluate the population pharmacokinetic properties of emodepside. Logistic regression modeling was used to link exposure to drug-related treatment-emergent adverse events (TEAEs). Emodepside pharmacokinetics were well described by a transit-absorption model, followed by a 3-compartment disposition model. Body weight was included as an allometric function and both food and formulation had a significant impact on absorption rate and relative bioavailability. All drug-related TEAEs were transient, and mild or moderate in severity. An increase in peak plasma concentration was associated with an increase in the odds of experiencing a drug-related TEAE of interest.<br><br>
<strong>Conclusions/Significance</strong><br>
Pharmacokinetic modeling and simulation was used to derive an optimized, body weight-based dosing regimen, which allows for achievement of extended emodepside exposures above target concentrations while maintaining acceptable tolerability margins.</p> |
| first_indexed | 2024-03-07T07:40:24Z |
| format | Journal article |
| id | oxford-uuid:13e1e36a-cfe4-4cc4-8279-3646d963cb91 |
| institution | University of Oxford |
| language | English |
| last_indexed | 2024-03-07T07:40:24Z |
| publishDate | 2022 |
| publisher | Public Library of Science |
| record_format | dspace |
| spelling | oxford-uuid:13e1e36a-cfe4-4cc4-8279-3646d963cb912023-04-20T09:19:11ZDrug development for the treatment of onchocerciasis: population pharmacokinetic and adverse events modeling of emodepsideJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:13e1e36a-cfe4-4cc4-8279-3646d963cb91EnglishSymplectic ElementsPublic Library of Science2022Assmus, FHoglund, RMMonnot, FSpecht, SScandale, ITarning, J<p><strong>Background</strong><br> To accelerate the progress towards onchocerciasis elimination, a macrofilaricidal drug that kills the adult parasite is urgently needed. Emodepside has shown macrofilaricidal activity against a variety of nematodes and is currently under clinical development for the treatment of onchocerciasis. The aims of this study were i) to characterize the population pharmacokinetic properties of emodepside, ii) to link its exposure to adverse events in healthy volunteers, and iii) to propose an optimized dosing regimen for a planned phase II study in onchocerciasis patients.<br><br> <strong>Methodology / Principal findings</strong><br> Plasma concentration-time profiles and adverse event data were obtained from 142 subjects enrolled in three phase I studies, including a single-dose, and a multiple-dose, dose-escalation study as well as a relative bioavailability study. Nonlinear mixed-effects modeling was used to evaluate the population pharmacokinetic properties of emodepside. Logistic regression modeling was used to link exposure to drug-related treatment-emergent adverse events (TEAEs). Emodepside pharmacokinetics were well described by a transit-absorption model, followed by a 3-compartment disposition model. Body weight was included as an allometric function and both food and formulation had a significant impact on absorption rate and relative bioavailability. All drug-related TEAEs were transient, and mild or moderate in severity. An increase in peak plasma concentration was associated with an increase in the odds of experiencing a drug-related TEAE of interest.<br><br> <strong>Conclusions/Significance</strong><br> Pharmacokinetic modeling and simulation was used to derive an optimized, body weight-based dosing regimen, which allows for achievement of extended emodepside exposures above target concentrations while maintaining acceptable tolerability margins.</p> |
| spellingShingle | Assmus, F Hoglund, RM Monnot, F Specht, S Scandale, I Tarning, J Drug development for the treatment of onchocerciasis: population pharmacokinetic and adverse events modeling of emodepside |
| title | Drug development for the treatment of onchocerciasis: population pharmacokinetic and adverse events modeling of emodepside |
| title_full | Drug development for the treatment of onchocerciasis: population pharmacokinetic and adverse events modeling of emodepside |
| title_fullStr | Drug development for the treatment of onchocerciasis: population pharmacokinetic and adverse events modeling of emodepside |
| title_full_unstemmed | Drug development for the treatment of onchocerciasis: population pharmacokinetic and adverse events modeling of emodepside |
| title_short | Drug development for the treatment of onchocerciasis: population pharmacokinetic and adverse events modeling of emodepside |
| title_sort | drug development for the treatment of onchocerciasis population pharmacokinetic and adverse events modeling of emodepside |
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