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Defining the therapeutic reference range for cariprazine

INTRODUCTION: According to the Consensus Guideline, the “therapeutic reference range” (TRR) defines ranges of drug blood concentrations that specify a lower limit below which a drug-induced therapeutic response is unlikely to occur and an upper limit above which tolerability decreases or the therape...

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Autores principales: Kapás, M., Horváth, A., Djuric, D., Csehi, R., Barabássy, Á.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10661137/
http://dx.doi.org/10.1192/j.eurpsy.2023.1178
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author Kapás, M.
Horváth, A.
Djuric, D.
Csehi, R.
Barabássy, Á.
author_facet Kapás, M.
Horváth, A.
Djuric, D.
Csehi, R.
Barabássy, Á.
author_sort Kapás, M.
collection PubMed
description INTRODUCTION: According to the Consensus Guideline, the “therapeutic reference range” (TRR) defines ranges of drug blood concentrations that specify a lower limit below which a drug-induced therapeutic response is unlikely to occur and an upper limit above which tolerability decreases or the therapeutic improvement ceases. The TRR can be obtained from concentration measurements (trough (pre-dose) plasma concentration under steady-state conditions) in studies at therapeutically effective doses. OBJECTIVES: The aim is to examine the TRR for cariprazine (CAR: 1.5 mg/day to 6 mg/day) in schizophrenia studies. METHODS: The population based TRR for CAR is derived by PK/PD evaluation from phase 2/3 schizophrenia efficacy studies with sparse PK sampling. The population PK simulated TRR is compared to the actually measured values obtained from two PK studies. As the two active metabolites of cariprazine also contribute to the drug effect, plasma exposure is given for Total cariprazine (CAR + DCAR + DDCAR) and the parent drug (CAR). RESULTS: PK/PD analyses demonstrated an increase in efficacy with increasing exposure. These efficacy results are related to Total cariprazine trough concentrations of ca. 30 nM and 100 nM that determine the lower and upper TRR limits. For the parent drug, the pre-dose mean plasma concentration at 6 mg/day was between 5.7-10 ng/mL in different studies, while at 1.5 mg/day it was 1.9 ng/mL. CONCLUSIONS: The TRR of the trough plasma levels at steady state is ca. 30 – 100 nM for Total cariprazine and ca. 2-10 ng/mL for the parent drug (unchanged drug) for schizophrenia treatment. DISCLOSURE OF INTEREST: M. Kapás Employee of: Gedeon Richter Plc., A. Horváth Employee of: Gedeon Richter Plc., D. Djuric Employee of: Gedeon Richter Plc., R. Csehi Employee of: Gedeon Richter Plc., Á. Barabássy Employee of: Gedeon Richter Plc.
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spelling pubmed-106611372023-07-19 Defining the therapeutic reference range for cariprazine Kapás, M. Horváth, A. Djuric, D. Csehi, R. Barabássy, Á. Eur Psychiatry Abstract INTRODUCTION: According to the Consensus Guideline, the “therapeutic reference range” (TRR) defines ranges of drug blood concentrations that specify a lower limit below which a drug-induced therapeutic response is unlikely to occur and an upper limit above which tolerability decreases or the therapeutic improvement ceases. The TRR can be obtained from concentration measurements (trough (pre-dose) plasma concentration under steady-state conditions) in studies at therapeutically effective doses. OBJECTIVES: The aim is to examine the TRR for cariprazine (CAR: 1.5 mg/day to 6 mg/day) in schizophrenia studies. METHODS: The population based TRR for CAR is derived by PK/PD evaluation from phase 2/3 schizophrenia efficacy studies with sparse PK sampling. The population PK simulated TRR is compared to the actually measured values obtained from two PK studies. As the two active metabolites of cariprazine also contribute to the drug effect, plasma exposure is given for Total cariprazine (CAR + DCAR + DDCAR) and the parent drug (CAR). RESULTS: PK/PD analyses demonstrated an increase in efficacy with increasing exposure. These efficacy results are related to Total cariprazine trough concentrations of ca. 30 nM and 100 nM that determine the lower and upper TRR limits. For the parent drug, the pre-dose mean plasma concentration at 6 mg/day was between 5.7-10 ng/mL in different studies, while at 1.5 mg/day it was 1.9 ng/mL. CONCLUSIONS: The TRR of the trough plasma levels at steady state is ca. 30 – 100 nM for Total cariprazine and ca. 2-10 ng/mL for the parent drug (unchanged drug) for schizophrenia treatment. DISCLOSURE OF INTEREST: M. Kapás Employee of: Gedeon Richter Plc., A. Horváth Employee of: Gedeon Richter Plc., D. Djuric Employee of: Gedeon Richter Plc., R. Csehi Employee of: Gedeon Richter Plc., Á. Barabássy Employee of: Gedeon Richter Plc. Cambridge University Press 2023-07-19 /pmc/articles/PMC10661137/ http://dx.doi.org/10.1192/j.eurpsy.2023.1178 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Abstract
Kapás, M.
Horváth, A.
Djuric, D.
Csehi, R.
Barabássy, Á.
Defining the therapeutic reference range for cariprazine
title Defining the therapeutic reference range for cariprazine
title_full Defining the therapeutic reference range for cariprazine
title_fullStr Defining the therapeutic reference range for cariprazine
title_full_unstemmed Defining the therapeutic reference range for cariprazine
title_short Defining the therapeutic reference range for cariprazine
title_sort defining the therapeutic reference range for cariprazine
topic Abstract
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10661137/
http://dx.doi.org/10.1192/j.eurpsy.2023.1178
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