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Antiepileptic Drug

University of Aberdeen • Épilepsie

Suivi actif À vérifier

Résumé

Antiepileptic Drug est développé par University of Aberdeen. Le traitement est actuellement en À vérifier. Il est associé à Épilepsie. . Le statut actuel est : suivi actif.

À vérifier

Non renseigné
À vérifier
University of Aberdeen
Non renseigné
People with epilepsy are predisposed to having seizures ("fits"), where abnormal electrical activity in the brain disrupts normal brain functioning. It is a common condition with around 1% of the population of Scotland having this condition. They are treated with anti-seizure medications, drugs which reduce the chance of having seizures. Unfortunately, people with epilepsy are more likely to have severe infections than those without epilepsy and this is known to increase risk of seizures. The reasons for more severe infections in people with epilepsy are unclear, but one factor may be that anti-seizure medications impair the function of the body's immune system, which fights infection. The investigators' previous work looking at residents in the North-East of Scotland showed a link between these medications and risk of infection. The investigators plan to study people being started on antiseizure medications (ASMs) with a new diagnosis of epilepsy and those already on ASMs with an established diagnosis of epilepsy in NHS Grampian. The investigators will compare with people not taking ASMs in a group of people with a single seizure and in a group of people with migraine. The investigators will investigate immune function and infection risk with more-detailed information about individual's background, their seizures/epilepsy, other health conditions, and blood tests. The investigators will then do laboratory experiments to determine how ASMs may impair the immune system by looking at the function of types of white blood cells that play an important part in immune functioning. The investigators also wish to develop statistical tools which can identify an individual's risk of infection when starting ASMs, based on their demographic, medical and social characteristics, to target closer monitoring/changes in treatment to those with higher risk. This research will allow healthcare professionals to provide better individualised care in terms of which medication to use for treatment, what doses to use and whether blood tests to screen for impaired immune function would be helpful. The aim is that this will lead to reduced risk of infections in people with epilepsy, resulting in better outcomes in this condition.
2026-10-29

Début phase actuelle
Non disponible dans les sources synchronisées
Timeline clinique

À vérifier
Préclinique
Phase 1
Phase 2
Phase 3
Approuvé

Objectif scientifique de l’étude

classification automatique vérifiable
Confiance automatique : 59%

Description affichée depuis l’essai compatible NCT07903168, afin d’éviter le mélange entre plusieurs indications d’une même molécule.

Contrôle de cohérence : 85/100

L’objectif est absent ou classé « Autre » et doit être recalculé à partir du protocole.

Transparence et qualité de la fiche

données vérifiables
ClassificationÀ vérifier
Confiance de la fiche85 %
Source principaleSource officielle ou publication indexée
Dernière vérification2026-10-29
Anomalies détectées1
Validation humaineValidation humaine non effectuée
Donnée issue d’une source Donnée normalisée automatiquement Interprétation algorithmique

Classification scientifique multi-axes

ne pas confondre statut et résultat
État de l’étudeRecrutement en cours
Disponibilité des résultatsRésultats à vérifier
InterprétationImpossible à déterminer
Niveau de preuveNon évaluable

Un essai terminé n’est pas nécessairement positif. Un essai arrêté n’est classé comme échec scientifique que lorsqu’un résultat ou une raison explicite le confirme.

Indicateurs factuels

sans score subjectif
Phase enregistréeÀ vérifier
Études associées1
Publications associées13
Statut consolidéSuivi actif

Aucune chance de succès, note d’innovation, potentiel thérapeutique ou probabilité de commercialisation n’est calculé tant qu’un modèle validé et des données suffisantes ne sont pas disponibles.

Historique factuel de la molécule

18 événement(s) daté(s)

Cette liste reprend uniquement les dates trouvées dans les registres et publications liés. Elle ne constitue pas une prévision.

DateÉvénementSource
2026-07-08PublicationProgress report on new antiepileptic drugs: a summary of the Ninth Eilat Conference (EILAT IX).Epilepsy research
2026-07-08PublicationA review of the efficacy and safety of eslicarbazepine acetate in the management of partial-onset seizures.Therapeutic advances in neurological disorders
2026-07-14PublicationAn Unusual Genetic Variant of Long QT Syndrome with Late Presentation in the Sixth Decade.The Journal of innovations in cardiac rhythm management
2026-08-08PublicationEpileptic Encephalopathy After Human Herpes Virus 6-Related Post-Transplant Acute Limbic Encephalitis in Children: A Case Report and Review of the Literature.Cureus
2026-08-08PublicationLacosamide Use After Traumatic Brain Injury: A Scoping Review.Cureus
2026-08-13PublicationAntiseizure medication use in pregnancy and the risk of poor fetal growth in the EURAP international registry: a prospective cohort study.The Lancet. Neurology
2026-08-16PublicationVoltage-gated sodium channels in the nervous system: Molecular physiology to therapeutic interventions.Neural regeneration research
2026-08-16PublicationA phase I, randomized, open-label, single-dose, 3-period crossover study to evaluate the drug-drug interaction between ZX008 (fenfluramine HCl oral solution) and a regimen of stiripentol, clobazam, and valproate in healthy subjects
.International journal of clinical pharmacology and therapeutics
2026-08-16PublicationPotassium Channelopathies and Precision Medicine Approaches in Epilepsy: A Systematic Review of Personalized Treatment Strategies.Current neuropharmacology
2026-08-16PublicationProgress report on new epilepsy treatments: A summary of the Eighteenth Eilat Conference on New Antiepileptic Drugs and Devices (EILAT XVIII). II. Treatments in more advanced clinical development.Epilepsia
2026-08-16PublicationClinical drug-oriented design, synthesis, and pharmacological evaluation of novel dual-target antiepileptic hybrid molecules.Bioorganic chemistry
2026-08-16PublicationEffect of renal impairment on the pharmacokinetics of eslicarbazepine acetate.International journal of clinical pharmacology and therapeutics
2026-08-16PublicationAntiseizure Medications that Did Not Reach the Epilepsy Market: An Assessment of Factors Contributing to Their Failed Clinical Development Over the Last Three Decades.Drugs
2026-10-29Dernière mise à jour des donnéesAntiepileptic DrugBiomedical Watch
2026-11-01Début de l’étudeNCT07903168Registre d’essai clinique
2026-11-01Création de l’enregistrementNCT07903168Registre d’essai clinique
2026-11-08Dernière mise à jour du registreNCT07903168Registre d’essai clinique
2038-05-01Fin de l’étude prévue / enregistréeNCT07903168Registre d’essai clinique

Début phase actuelle
Non disponible dans les sources synchronisées
Essais cliniques liés

1 essai(s)
NCT Titre Phase Statut administratif Pays Sponsor
NCT07903168 Epi-IRIS — Why Do People With Epilepsy Get More Infections? À vérifier NOT_YET_RECRUITING Non communiqué University of Aberdeen

Publications liées

13 publication(s)

Publications liées

13 publication(s)
Titre PMID DOI Journal Date
Voltage-gated sodium channels in the nervous system: Molecular physiology to therapeutic interventions. Voir source 40808385 10.4103/NRR.NRR-D-25-00260 Neural regeneration research
A phase I, randomized, open-label, single-dose, 3-period crossover study to evaluate the drug-drug interaction between ZX008 (fenfluramine HCl oral solution) and a regimen of stiripentol, clobazam, and valproate in healthy subjects
. Voir source 30336805 10.5414/CP203276 International journal of clinical pharmacology and therapeutics
Potassium Channelopathies and Precision Medicine Approaches in Epilepsy: A Systematic Review of Personalized Treatment Strategies. Voir source 42003125 10.2174/011570159X407197251204124232 Current neuropharmacology
Progress report on new epilepsy treatments: A summary of the Eighteenth Eilat Conference on New Antiepileptic Drugs and Devices (EILAT XVIII). II. Treatments in more advanced clinical development. Voir source 42470359 10.1002/epi.70346 Epilepsia
Clinical drug-oriented design, synthesis, and pharmacological evaluation of novel dual-target antiepileptic hybrid molecules. Voir source 42385394 10.1016/j.bioorg.2026.110159 Bioorganic chemistry
Effect of renal impairment on the pharmacokinetics of eslicarbazepine acetate. Voir source 18397682 10.5414/cpp46119 International journal of clinical pharmacology and therapeutics
Antiseizure Medications that Did Not Reach the Epilepsy Market: An Assessment of Factors Contributing to Their Failed Clinical Development Over the Last Three Decades. Voir source 41764707 10.1007/s40265-026-02297-y Drugs
Antiseizure medication use in pregnancy and the risk of poor fetal growth in the EURAP international registry: a prospective cohort study. Voir source 42586099 10.1016/S1474-4422(26)00216-4 The Lancet. Neurology
Epileptic Encephalopathy After Human Herpes Virus 6-Related Post-Transplant Acute Limbic Encephalitis in Children: A Case Report and Review of the Literature. Voir source 40546590 10.7759/cureus.84647 Cureus
Lacosamide Use After Traumatic Brain Injury: A Scoping Review. Voir source 42558887 10.7759/cureus.112117 Cureus
An Unusual Genetic Variant of Long QT Syndrome with Late Presentation in the Sixth Decade. Voir source 42405015 10.19102/icrm.2026.17064 The Journal of innovations in cardiac rhythm management
Progress report on new antiepileptic drugs: a summary of the Ninth Eilat Conference (EILAT IX). Voir source 19008076 10.1016/j.eplepsyres.2008.09.005 Epilepsy research
A review of the efficacy and safety of eslicarbazepine acetate in the management of partial-onset seizures. Voir source 26136845 10.1177/1756285615589711 Therapeutic advances in neurological disorders

Sources officielles

liens de recherche

Dernière mise à jour des données : 2026-10-29

Ces sources sont proposées pour vérification. Les informations de la fiche doivent être confirmées dans les registres officiels ou les publications originales.