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Disease

Seizures

Late-stage therapeutic developmentActively researchedRising momentum
40
Publications
23
Clinical trials
9
Related conditions
3
Related treatments
2
Related proteins
2025
Latest publication
Current focus
Therapeutic developmentGenetics & risk factorsInflammation & immunity
Latest activity
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Recent clinical, regulatory, research and industry developments relating to this disease.

The critical dynamics of hippocampal seizures.

Research2024-08-13Nature communications

SV2B defines a subpopulation of synaptic vesicles.

Research2024-04-01Journal of molecular cell biology

Antiepileptic Strategies for Patients with Primary and Metastatic Brain Tumors.

Research2024-02-14Current treatment options in oncology

Approval: Ztalmy (EMA)

Regulatory2023-07-26EMA

Approval: Fintepla (EMA)

Regulatory2020-12-18EMA

Approval: Epidyolex (EMA)

Regulatory2019-09-19EMA

What's happening now

An analyst briefing on current research, clinical, regulatory and industry activity surrounding this disease.

Clinical Milestones8View
Activity timeline8

Therapeutic landscape

Therapies with a regulatory footing for this condition, alongside the wider set of agents co-studied with it in the literature.

Approved & established therapies
Ganaxoloneapproved

Approval — Ztalmy is indicated for the adjunctive treatment of epileptic seizures associated with cy… (2023)

Lacosamideapproved

Approval — Lacosamide Adroiq is indicated as monotherapy in the treatment of partial-onset seizures… (2023)

Cenobamateapproved

Approval — Adjunctive treatment of focal-onset seizures with or without secondary generalisation in… (2021)

Approval — Treatment of seizures associated with Dravet syndrome as an add-on therapy to other antie… (2020)

Cannabidiolapproved

Approval — Epidyolex is indicated for use as adjunctive therapy of seizures associated with Lennox G… (2019)

Vigabatrinapproved

Approval — Kigabeq is indicated in infants and children from 1 month to less than 7 years of age for… (2018)

Research-associated treatments

Clinical trials

13 sponsors · 2 new · 3 completed in the last 12 months (net +2)

The current development programme across all trial phases.

Clinical programme
23
All trials
6
Active
18
Late-stage
6
Completed
Late-stage studies
Recruiting
Recently completed

Regulatory timeline

Drug regulatory events matched to this condition by indication — EMA.

First approvals
2023emaApprovalGanaxolone· Ztalmy is indicated for the adjunctive treatment of epileptic seizures associated with cyclin-dependent kinase-like 5 (CDKL5) deficiency disorder (CDD) in patients 2 to 17 years of age. Ztalmy may be continued in patients 18 years of age and older. source ↗
2023emaApprovalLacosamide· Lacosamide Adroiq is indicated as monotherapy in the treatment of partial-onset seizures with or without secondary generalisation in adults, adolescents and children from 2 years of age with epilepsy. Lacosamide Adroiq is indicated as adjunctive therapy in the treatment of partial-onset seizures with or without secondary generalisation in adults, adolescents and children from 2 years of age with epilepsy. in the treatment of primary generalised tonic-clonic seizures in adults, adolescents and children from 4 years of age with idiopathic generalised epilepsy. source ↗
2021emaApprovalCenobamate· Adjunctive treatment of focal-onset seizures with or without secondary generalisation in adult patients with epilepsy who have not been adequately controlled despite a history of treatment with at least 2 anti-epileptic medicinal products. source ↗
2020emaApprovalFenfluramine hydrochloride· Treatment of seizures associated with Dravet syndrome as an add-on therapy to other antiepileptic medicines for patients 2 years of age and older. Fintepla is indicated for the treatment of seizures associated with Dravet syndrome and Lennox-Gastaut syndrome as an add-on therapy to other anti-epileptic medicines for patients 2 years of age and older. source ↗
2019emaApprovalCannabidiol· Epidyolex is indicated for use as adjunctive therapy of seizures associated with Lennox Gastaut syndrome (LGS) or Dravet syndrome (DS), in conjunction with clobazam, for patients 2 years of age and older. source ↗
2019emaApprovalLacosamide· Lacosamide UCB is indicated as monotherapy and adjunctive therapy in the treatment of partial-onset seizures with or without secondary generalisation in adults, adolescents and children from 4 years of age with epilepsy. source ↗
2018emaApprovalVigabatrin· Kigabeq is indicated in infants and children from 1 month to less than 7 years of age for: Treatment in monotherapy of infantile spasms (West's syndrome). Treatment in combination with other antiepileptic medicinal products for patients with resistant partial epilepsy (focal onset seizures) with or without secondary generalisation, that is where all other appropriate medicinal product combinations have proved inadequate or have not been tolerated. source ↗
2017emaApprovalLacosamide· Lacosamide Accord is indicated as monotherapy in the treatment of partial-onset seizures with or without secondary generalisation in adults, adolescents and children from 4 years of age with epilepsy. Lacosamide Accord is indicated as adjunctive therapy •         in the treatment of partial-onset seizures with or without secondary generalisation in adults, adolescents and children from 4 years of age with epilepsy. •         in the treatment of primary generalised tonic-clonic seizures in adults, adolescents and children from 4 years of age with idiopathic generalised epilepsy. source ↗
Safety updates
2023emaMarket withdrawalPregabalin· Epilepsy Pregabalin Sandoz GmbH is indicated as adjunctive therapy in adults with partial seizures with or without secondary generalisation. Generalised Anxiety Disorder Pregabalin Sandoz GmbH is indicated for the treatment of Generalised Anxiety Disorder (GAD) in adults. source ↗

European Medicines Agency (CC BY 4.0). Events are matched to this condition by drug indication text — approvals/updates for drugs indicated for it, not disease-specific acts.

Research activity

40 papers

Key research shaping understanding of this disease, combining the latest publications with the most influential evidence.

Publications over time
20052025
Most influential
Recent publications
Major themes8
  • Epilepsy15
  • Seizures6
  • Status Epilepticus4
  • Brain Neoplasms2
  • Deep Brain Stimulation2
  • Genetic Therapy2
  • Hippocampus2
  • MicroRNAs2
Leading journals6
  • Epilepsia6
  • The Journal of pharmacology and experimental therapeutics3
  • International journal of molecular sciences2
  • Nature communications2
  • The Journal of neuroscience : the official journal of the Society for Neuroscience2
  • The New England journal of medicine2
Leading researchers8
  • Auvin S3
  • Ramakrishnan S3
  • Reddy DS3
  • Singh T3
  • Specchio N3
  • Wiebe S3
  • Wu X3
  • Bartolomei F2
Affiliations (unnormalised)6
  • Mayo Clinic6
  • Department of Clinical Neurosciences3
  • Red Cross War Memorial Children's Hospital3
  • School of Medicine3
  • University of Melbourne3
  • Aga Khan University2

Disease biology

2 matches

Key proteins & gene products studied in this disease. Number shows shared papers.

Related conditions

9 matches

Diseases frequently studied alongside this one. Number shows shared papers.

Disease profile

A grounded synthesis of the condition — overview, causes, mechanism, risk factors and current standard of care.

Overview

Seizures are clinical or subclinical disturbances of cortical function caused by a sudden, abnormal, excessive, and disorganized discharge of brain cells. They can produce abnormal motor, sensory, and psychic phenomena. Recurrent seizures are generally referred to as epilepsy or seizure disorder.

Causes

The supplied grounding supports several associated causes or contexts, including chemically induced seizures and seizures related to brain tumors. It also supports seizures occurring in functional neurologic disorder as involuntary neurologic symptoms, and in broader epileptic disorders where inflammatory, genetic, and tumor-related mechanisms are discussed. No single universal cause is established in the grounding.

Pathophysiology

The core mechanism is abnormal, excessive, and disorganized cortical neuronal discharge. Inflammatory reactions in the brain can enhance neuronal excitability, impair neuronal survival, and increase blood-brain barrier permeability, which may promote seizures. Impaired KCC2 function can disrupt chloride homeostasis, weaken GABAergic inhibition, and contribute to epileptic activity; shared mechanisms with tumor growth and epilepsy are also noted in tumor-related epilepsy.

Risk factors

The grounding supports increased seizure risk in the setting of brain tumors, inflammatory CNS disease, and conditions associated with posterior reversible encephalopathy syndrome such as preeclampsia/eclampsia, transplantation, autoimmune disease, and high-dose cancer chemotherapy. It also supports genetic contributions and sex characteristics as studied modifiers, but does not provide specific risk estimates. No additional risk factors are supported by the supplied material.

Current standard of care

Treatment is described at the level of antiseizure medications, often used in conjunction with surgery and/or chemoradiotherapy for tumor-related epilepsy. Gross total resection is favored in brain tumor-related epilepsy from both oncologic and epilepsy perspectives. The grounding also supports broader drug therapy and surgery as management modalities, but does not specify particular regimens.

AI-generated summary grounded in MeSH and 6 peer-reviewed sources. Informational only — not medical advice. Generated 2026-07-07.

Reference

Authoritative identity, definition & identifiers.

Defined in MeSH

Clinical or subclinical disturbances of cortical function due to a sudden, abnormal, excessive, and disorganized discharge of brain cells. Clinical manifestations include abnormal motor, sensory and psychic phenomena. Recurrent seizures are usually referred to as EPILEPSY or seizure disorder.

Identifiers
References & data sources
  • Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
  • Clinical trials — ClinicalTrials.gov (U.S. National Library of Medicine)
  • Research activity — Europe PMC (EMBL-EBI) + OpenAlex-derived paper links
  • Related entities are derived from literature co-mention (studied together) — associative, not causal.