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Disease

Epilepsy

Late-stage therapeutic developmentActively researchedCooling momentum
54
Publications
24
Clinical trials
12
Related conditions
1
Related treatments
2
Related proteins
2026
Latest publication
Latest activity
beta

Recent clinical, regulatory, research and industry developments relating to this disease.

Invasive Neurostimulation for the Treatment of Epilepsy.

Research2025-03-19Seminars in neurology

Epilepsy and Cardiac Arrhythmias: A State-of-the-Art Review.

Research2024-11-20JACC. Clinical electrophysiology

The critical dynamics of hippocampal seizures.

Research2024-08-13Nature communications

Approval: Lacosamide Adroiq (EMA)

Regulatory2023-05-31EMA

Approval: Ontozry (EMA)

Regulatory2021-03-26EMA

What's happening now

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

Research Highlights2View
Clinical Milestones11View all 11
+3 more in the activity timeline below
Industry & Market2View
Activity timeline15

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
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)

Vigabatrinapproved

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

Brivaracetamapproved

Approval — Briviact is indicated as adjunctive therapy in the treatment of partial-onset seizures wi… (2016)

Zonisamideapproved

Approval — Monotherapy in the treatment of partial seizures, with or without secondary generalisatio… (2016)

Pregabalinapproved

Approval — Epilepsy Pregabalin Accord is indicated as adjunctive therapy in adults with partial sei… (2015)

Research-associated treatments

Clinical trials

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

The current development programme across all trial phases.

Clinical programme
24
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
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 ↗
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 ↗
2016emaApprovalZonisamide· Monotherapy in the treatment of partial seizures, with or without secondary generalisation, in adults with newly diagnosed epilepsy; adjunctive therapy in the treatment of partial seizures, with or without secondary generalisation, in adults, adolescents, and children aged 6 years and above. source ↗
2016emaApprovalBrivaracetam· Briviact is indicated as adjunctive therapy in the treatment of partial-onset seizures with or without secondary generalisation in adult and adolescent patients from 16 years of age with epilepsy. source ↗
2015emaApprovalPregabalin· Epilepsy Pregabalin Accord is indicated as adjunctive therapy in adults with partial seizures with or without secondary generalisation. Generalised Anxiety Disorder Pregabalin Accord is indicated for the treatment of Generalised Anxiety Disorder (GAD) in adults. 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

54 papers

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

Publications over time
20132026
Most influential
Major themes8
  • Epilepsy36
  • Deep Brain Stimulation5
  • Electroencephalography4
  • Vagus Nerve Stimulation4
  • Alzheimer Disease3
  • Brain Neoplasms2
  • Brain-Computer Interfaces2
  • Cannabidiol2
Leading journals6
  • Epilepsia8
  • Nature communications3
  • Brain stimulation2
  • International journal of molecular sciences2
  • Journal of neuroinflammation2
  • The Journal of neuroscience : the official journal of the Society for Neuroscience2
Leading researchers8
  • Denison T3
  • Lundstrom BN3
  • Wiebe S3
  • Auvin S2
  • Bartoli E2
  • Bartolomei F2
  • Baud MO2
  • Beniczky S2
Affiliations (unnormalised)6
  • Mayo Clinic8
  • Baylor College of Medicine3
  • School of Medicine3
  • Aarhus University Hospital2
  • Department of Clinical and Experimental Epilepsy2
  • Department of Clinical Neurophysiology2

Disease biology

2 matches

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

Related conditions

12 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

Epilepsy is a disorder marked by recurrent episodes of paroxysmal brain dysfunction caused by sudden, disordered, and excessive neuronal discharge. The literature also treats it as a heterogeneous condition that can be classified by seizure features, cause, anatomic origin, spread, and temporal pattern.

Causes

The supplied grounding supports multiple etiologic contributors rather than a single cause. Epilepsy is often associated with prior lesions or injury in the nervous system, and inflammatory processes in injured neural tissue are described as important in its development. Glutamate-mediated neuronal hyperexcitation is also described as a causative factor in seizure generation.

Pathophysiology

The core mechanism is excessive neuronal discharge leading to recurrent seizures. Grounding highlights glutamate-mediated hyperexcitation, especially through AMPA and NMDA receptors, as well as inflammatory signaling that can increase neuronal excitability, impair cell survival, and increase blood-brain barrier permeability. The literature also links epilepsy-related biology to signal transduction, neuronal plasticity, action potentials, oxidative stress, and pathways involving protein serine-threonine kinases including TOR serine-threonine kinases.

Risk factors

Prior lesions in the nervous system are described as commonly associated with epilepsy. The literature also supports inflammatory states in the brain or systemic disorders as contributors to epilepsy development, and sleep deprivation is presented as a factor that negatively affects brain function and is relevant to neurological disorders. No additional risk factors are supported by the supplied grounding.

Current standard of care

The supplied grounding supports antiseizure drug therapy and non-drug neuromodulation approaches. Cannabidiol is specifically co-studied, and the literature also discusses glutamate receptor antagonism as a therapeutic strategy, with perampanel noted as an approved AMPA-receptor antagonist. Vagus nerve stimulation is described as a nondrug therapy, and surgery is included among the covered management modalities, but no further treatment specifics are supported here.

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

A disorder characterized by recurrent episodes of paroxysmal brain dysfunction due to a sudden, disorderly, and excessive neuronal discharge. Epilepsy classification systems are generally based upon: (1) clinical features of the seizure episodes (e.g., motor seizure), (2) etiology (e.g., post-traumatic), (3) anatomic site of seizure origin (e.g., frontal lobe seizure), (4) tendency to spread to other structures in the brain, and (5) temporal patterns (e.g., nocturnal epilepsy). (From Adams et al., Principles of Neurology, 6th ed, p313)

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.