Evidence map›Paper›PMID 38811492›Full record

ReviewAdvances in therapy2024

Narrative Review of Brivaracetam: Preclinical Profile and Clinical Benefits in the Treatment of Patients with Epilepsy.

Pavel Klein, Dimitrios Bourikas

7 registry-linked trialsAbstract readReview
In one paragraph

Review in Advances in therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 7 registered trials, which are not on this map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT00150800 phase3completednot on this map

An Open-label, Multi-center, Follow-up Trial to Evaluate Long Term Safety and Efficacy of Brivaracetam Used as Adjunctive Treatment at a Flexible Dose up to a Maximum of 200 mg/Day in Subjects Aged 16 Years or Older Suffering From Epilepsy

TypeinterventionalSponsorUCB PHARMA Inc. (US)Ran2006 to 2017Enrolled668ConditionsEpilepsyArmsBrivaracetam
NCT00175916 phase3completednot on this map

An Open-label, Multicenter, Follow-up Trial to Evaluate Long-term Safety and Efficacy of Brivaracetam Used as Adjunctive Treatment at a Flexible Dose up to a Maximum of 200 mg/Day in Subjects Aged 16 Years or Older Suffering From Epilepsy

TypeinterventionalSponsorUCB PharmaRan2005 to 2019Enrolled853ConditionsEpilepsyArmsBrivaracetam (ucb 34714)
NCT00464269 phase3completednot on this map

An International, Double-blind, Parallel-group, Placebo-controlled, Randomized Study: Evaluation of the Efficacy and Safety of Brivaracetam in Subjects (>= 16 to 70 Years Old) With Partial Onset Seizures

TypeinterventionalSponsorUCB PharmaRan2007 to 2009Enrolled400ConditionsEpilepsyArmsPlacebo, Brivaracetam 2.5 mg, Brivaracetam 10 mg, Brivaracetam 25 mg
NCT00490035 phase3completednot on this map

A Multi-center, Double-blind, Parallel-group, Placebo Controlled, Randomized Study: Evaluation of the Efficacy and Safety of Brivaracetam in Subjects (>= 16 to 70 Years Old) With Partial Onset Seizures.

TypeinterventionalSponsorUCB Pharma SARan2007 to 2009Enrolled399ConditionsEpilepsyArmsPlacebo, Brivaracetam
NCT01261325 phase3completednot on this map

A Randomized, Double-blind, Placebo-controlled, Multicenter, Parallel-group Study to Evaluate the Efficacy and Safety of Brivaracetam in Subjects (≥16 to 80 Years Old) With Partial Onset Seizures

TypeinterventionalSponsorUCB PharmaRan2010 to 2014Enrolled768ConditionsEpilepsyArmsPlacebo, Brivaracetam, Antiepileptic drugs with market authorization available per country
NCT01339559 phase3completednot on this map

An Open-label, Multicenter, Follow-up Study to Evaluate the Long-term Safety and Efficacy of Brivaracetam Used as Adjunctive Treatment in Subjects Aged 16 Years or Older With Epilepsy

TypeinterventionalSponsorUCB BIOSCIENCES, Inc.Ran2011 to 2019Enrolled767ConditionsEpilepsyArmsBrivaracetam
NCT03083665 phase3completednot on this map

A Randomized, Double-blind, Placebo-controlled, Multicenter, Parallel-group Study to Evaluate the Efficacy and Safety of Adjunctive Brivaracetam in Subjects (>=16 to 80 Years of Age) With Partial Seizures With or Without Secondary Generalization

TypeinterventionalSponsorUCB Biopharma SRLRan2017 to 2022Enrolled449ConditionsPartial Seizures With or Without Secondary Generalization, EpilepsyArmsPlacebo, Brivaracetam
3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

  1. Trial
  2. Review
  3. Article
  4. Brivaracetam-associated manic episode in a patient with bipolar disorder: A case report.PCN reports : psychiatry and clinical neurosciences · 2026
    Article
  5. Review
  6. Article
  7. Observational
  8. Article
  9. Review
  10. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Pavel KleinMid-Atlantic Epilepsy and Sleep Center, 6410 Rockledge Dr, Bethesda, MD, 20817, USA. kleinp@epilepsydc.com.ORCID 0000-0001-7244-3722
Dimitrios BourikasUCB Pharma, Agiou Dimitriou 63, 17456, Alimos, Greece.ORCID 0009-0005-4503-0734

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

One third of patients with epilepsy will continue to have uncontrolled seizures despite treatment with antiseizure medications (ASMs). There is therefore a need to develop novel ASMs. Brivaracetam (BRV) is an ASM that was developed in a major drug discovery program aimed at identifying selective, high-affinity synaptic vesicle protein 2A (SV2A) ligands, the target molecule of levetiracetam. BRV binds to SV2A with 15- to 30-fold higher affinity and greater selectivity than levetiracetam. BRV has broad-spectrum antiseizure activity in animal models of epilepsy, a favorable pharmacokinetic profile, few clinically relevant drug-drug interactions, and rapid brain penetration. BRV is available in oral and intravenous formulations and can be initiated at target dose without titration. Efficacy and safety of adjunctive BRV (50-200 mg/day) treatment of focal-onset seizures was demonstrated in three pivotal phase III trials (NCT00490035/NCT00464269/NCT01261325), including in patients who had previously failed levetiracetam. Efficacy and safety of adjunctive BRV were also demonstrated in adult Asian patients with focal-onset seizures (NCT03083665). In several open-label trials (NCT00150800/NCT00175916/NCT01339559), long-term safety and tolerability of adjunctive BRV was established, with efficacy maintained for up to 14 years, with high retention rates. Evidence from daily clinical practice highlights BRV effectiveness and tolerability in specific epilepsy patient populations with high unmet needs: the elderly (≥ 65 years of age), children (< 16 years of age), patients with cognitive impairment, patients with psychiatric comorbid conditions, and patients with acquired epilepsy of specific etiologies (post-stroke epilepsy/brain tumor related epilepsy/traumatic brain injury-related epilepsy). Here, we review the preclinical profile and clinical benefits of BRV from pivotal trials and recently published evidence from daily clinical practice.

Indexed as

AnticonvulsantsEpilepsyPyrrolidinonesAdultAnimalsChildDrug Evaluation, PreclinicalHumansTreatment OutcomeAnticonvulsantsbrivaracetamPyrrolidinonesAntiseizure medicationComorbiditiesDrug-drug interactionsEffectivenessElderlyFast responseFocal-onset seizuresReal-world evidenceSV2ATolerability

Identifiers

PMID38811492
PMCPMC11213745

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

and 1 more above

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.