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Autori principali: Catherine M. K. E. de Cuba, Annika A. de Goede, Erica S. Klaassen, Marije E. Otto, Robert J. Doll, Jessica Kim, Mark A. Demitrack, Ruihua Chen, Geert Jan Groeneveld, Jules A. A. C. Heuberger
Natura: Artículo Open Access
Pubblicazione: Wiley 2024
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Accesso online:https://ascpt.onlinelibrary.wiley.com/doi/10.1002/cpt.3521
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author Catherine M. K. E. de Cuba
Annika A. de Goede
Erica S. Klaassen
Marije E. Otto
Robert J. Doll
Jessica Kim
Mark A. Demitrack
Ruihua Chen
Geert Jan Groeneveld
Jules A. A. C. Heuberger
author_facet Catherine M. K. E. de Cuba
Annika A. de Goede
Erica S. Klaassen
Marije E. Otto
Robert J. Doll
Jessica Kim
Mark A. Demitrack
Ruihua Chen
Geert Jan Groeneveld
Jules A. A. C. Heuberger
Catherine M. K. E. de Cuba
Annika A. de Goede
Erica S. Klaassen
Marije E. Otto
Robert J. Doll
Jessica Kim
Mark A. Demitrack
Ruihua Chen
Geert Jan Groeneveld
Jules A. A. C. Heuberger
collection Wiley Open Access
contents TMS and EEG Pharmacodynamic Effects of a Selective Sphingosine‐1‐Phosphate Subtype 1 Receptor Agonist on Cortical Excitability in Healthy Subjects Catherine M. K. E. de Cuba Annika A. de Goede Erica S. Klaassen Marije E. Otto Robert J. Doll Jessica Kim Mark A. Demitrack Ruihua Chen Geert Jan Groeneveld Jules A. A. C. Heuberger Clinical Pharmacology & Therapeutics Current anti‐epileptic drugs lack efficacy, cause many side effects and one third of all patients are treatment‐resistant. Drugs targeting the sphingosine‐1‐phosphate receptor show potential anti‐convulsant effects in animal models and decrease cortical excitability in patients with multiple sclerosis, but available compounds alter lymphocyte trafficking and cause immunosuppression, limiting their clinical anti‐epileptic potential. TRV045 is a selective sphingosine‐1‐phosphate subtype 1 receptor agonist without effects on lymphocyte trafficking, demonstrating efficacy in animal models of epilepsy, with the potential to target abnormal cortical excitability. This randomized, double‐blind, placebo‐controlled, two‐way cross‐over, multiple‐dose study evaluated the effects of TRV045 on cortical excitability in healthy male adults, measured by pharmaco‐electroencephalography and transcranial magnetic stimulation (TMS). Subjects received TRV045 250 mg or placebo, once daily for 4 days, in randomized order. Endpoints were analyzed with a mixed effects model analysis of covariance. Twenty‐five of the 27 subjects completed the study. There was a significant increase in alpha power with eyes open after treatment with TRV045 on Day 1, increasing after 4 days of dosing. Less pronounced significant effects in beta, gamma, and delta power were observed after 4 days. For TMS‐Electromyography there was a non‐significant decreased post‐dose single‐pulse peak‐to‐peak amplitude on Day 1 only, and there were no effects on paired‐pulse parameters. Several significant TMS‐Electroencephalography clusters were seen after 4 days of dosing. These findings show that TRV045 has central nervous system activity with evolving effects following repeated dosing. These data support further studies to elucidate the mechanism of action of TRV045 and its potential anti‐epileptic effects. 10.1002/cpt.3521 http://creativecommons.org/licenses/by-nc/4.0/
doi_str_mv 10.1002/cpt.3521
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spellingShingle TMS and EEG Pharmacodynamic Effects of a Selective Sphingosine‐1‐Phosphate Subtype 1 Receptor Agonist on Cortical Excitability in Healthy Subjects
Catherine M. K. E. de Cuba
Annika A. de Goede
Erica S. Klaassen
Marije E. Otto
Robert J. Doll
Jessica Kim
Mark A. Demitrack
Ruihua Chen
Geert Jan Groeneveld
Jules A. A. C. Heuberger
Clinical Pharmacology & Therapeutics
TMS and EEG Pharmacodynamic Effects of a Selective Sphingosine‐1‐Phosphate Subtype 1 Receptor Agonist on Cortical Excitability in Healthy Subjects Catherine M. K. E. de Cuba Annika A. de Goede Erica S. Klaassen Marije E. Otto Robert J. Doll Jessica Kim Mark A. Demitrack Ruihua Chen Geert Jan Groeneveld Jules A. A. C. Heuberger Clinical Pharmacology & Therapeutics Current anti‐epileptic drugs lack efficacy, cause many side effects and one third of all patients are treatment‐resistant. Drugs targeting the sphingosine‐1‐phosphate receptor show potential anti‐convulsant effects in animal models and decrease cortical excitability in patients with multiple sclerosis, but available compounds alter lymphocyte trafficking and cause immunosuppression, limiting their clinical anti‐epileptic potential. TRV045 is a selective sphingosine‐1‐phosphate subtype 1 receptor agonist without effects on lymphocyte trafficking, demonstrating efficacy in animal models of epilepsy, with the potential to target abnormal cortical excitability. This randomized, double‐blind, placebo‐controlled, two‐way cross‐over, multiple‐dose study evaluated the effects of TRV045 on cortical excitability in healthy male adults, measured by pharmaco‐electroencephalography and transcranial magnetic stimulation (TMS). Subjects received TRV045 250 mg or placebo, once daily for 4 days, in randomized order. Endpoints were analyzed with a mixed effects model analysis of covariance. Twenty‐five of the 27 subjects completed the study. There was a significant increase in alpha power with eyes open after treatment with TRV045 on Day 1, increasing after 4 days of dosing. Less pronounced significant effects in beta, gamma, and delta power were observed after 4 days. For TMS‐Electromyography there was a non‐significant decreased post‐dose single‐pulse peak‐to‐peak amplitude on Day 1 only, and there were no effects on paired‐pulse parameters. Several significant TMS‐Electroencephalography clusters were seen after 4 days of dosing. These findings show that TRV045 has central nervous system activity with evolving effects following repeated dosing. These data support further studies to elucidate the mechanism of action of TRV045 and its potential anti‐epileptic effects. 10.1002/cpt.3521 http://creativecommons.org/licenses/by-nc/4.0/
title TMS and EEG Pharmacodynamic Effects of a Selective Sphingosine‐1‐Phosphate Subtype 1 Receptor Agonist on Cortical Excitability in Healthy Subjects
topic Clinical Pharmacology & Therapeutics
url https://ascpt.onlinelibrary.wiley.com/doi/10.1002/cpt.3521