Brivaracetam

drug
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Also known as BriviactBriviact (in italy: nubriveo)Briviact (in italy: nubriveo)UCB 34714UCB-34714UCB34714

Summary

Brivaracetam (CHEMBL607400) is an approved small-molecule anticonvulsant (ATC N03AX23) targeting SV2A; indicated across 9 conditions including epilepsy and visual epilepsy.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Small molecule
  • ATC class: N03AX23
  • Targets: 1 (SV2A)
  • Indications: 9 conditions
  • Clinical trials: 48
  • Chemistry: 212.29 Da · C11H20N2O2

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL607400
NameBrivaracetam
TypeSmall molecule
Max phase4
FDA approvedyes
PubChem CID9837243
ChEBICHEBI:133013
ATCN03AX23
Molecular formulaC11H20N2O2
Molecular weight212.29
InChIKeyMSYKRHVOOPPJKU-BDAKNGLRSA-N

SMILES: CCC[C@@H]1CC(=O)N(C1)[C@@H](CC)C(=O)N

IUPAC name: (2S)-2-[(4R)-2-oxo-4-propylpyrrolidin-1-yl]butanamide

ChEBI definition: A non-proteinogenic amino acid derivative that is butanamide in which the pro-S hydrogen at position 2 is replaced by a (4R)-2-oxo-4-propylpyrrolidin-1-yl. Used for treatment of partial onset seizures related to epilepsy.

Pharmacological roles (ChEBI): anticonvulsant.

Also known as: Brivaracetam, Briviact, Briviact (in italy: nubriveo), Briviact (in italy: nubriveo), UCB 34714, UCB-34714, UCB34714, BRIVARACETAM, BRIVIACT, BRIVIACT (IN ITALY: NUBRIVEO), BRIVIACT (IN ITALY: NUBRIVEO)

Patent coverage: 884 distinct patent families (2,743 SureChEMBL compound mentions), from 1 matched compound structure(s). Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.

Targets

Targets

Primary targets (GtoPdb curated mechanism): the Cancer dependency column is the DepMap CRISPR fitness signal (% of screened cell lines dependent on the target).

GeneTargetActionpAffinityCancer dependencyUniProt
SV2Asynaptic vesicle glycoprotein 2AInhibition75.6%Q7L0J3

Bioactivity

No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).

Target pathways

Aggregated over 1 target gene(s): SV2A.

Top Reactome pathways

9 total, by targets touching each:

PathwayTargetsGenes
Disease1SV2A
Neurotoxicity of clostridium toxins1SV2A
Toxicity of botulinum toxin type D (botD)1SV2A
Toxicity of botulinum toxin type A (botA)1SV2A
Toxicity of botulinum toxin type F (botF)1SV2A
Toxicity of botulinum toxin type E (botE)1SV2A
Uptake and actions of bacterial toxins1SV2A
Infectious disease1SV2A
Bacterial Infection Pathways1SV2A

Dominant GO biological processes

GO termTargets
intracellular calcium ion homeostasis1
synaptic vesicle priming1
neurotransmitter transport1
chemical synaptic transmission1
transmembrane transport1

Indications & clinical

Indications

9 indications (3 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).

IndicationTrial phaseMONDOEFO
epilepsy4MONDO:0005027EFO:0000474
visual epilepsy4MONDO:0001386HP:0001250
Unverricht-Lundborg syndrome3MONDO:0009698Orphanet:308
spinal cord injury1MONDO:0043797EFO:1001919
brain neoplasm0MONDO:0021211EFO:0003833

4 further indication records had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.

Clinical trials

Total trials: 48.

Phase distribution

PhaseTrials
PHASE324
PHASE28
PHASE18
Not specified5
PHASE1/PHASE22
EARLY_PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT04666610PHASE3ACTIVE_NOT_RECRUITINGA Study to Evaluate the Efficacy, Safety, and Tolerability of Brivaracetam as Monotherapy in Patients 2 to 25 Years of Age With Childhood Absence Epilepsy or Juvenile Absence Epilepsy
NCT04715646PHASE3RECRUITINGA Study to Test the Safety and Tolerability of Brivaracetam in Children and Adolescents With Seizures
NCT06315322PHASE3RECRUITINGA Study to Test the Long-term Safety and Tolerability of Brivaracetam in Study Participants With Childhood Absence Epilepsy or Juvenile Absence Epilepsy
NCT00150800PHASE3COMPLETEDThis Trial, Evaluating the Long-term Safety and Tolerability of Brivaracetam Will Provide Subjects Suffering From Epilepsy, Who May Have Benefited From Brivaracetam as Adjunctive Treatment, the Opportunity to Receive Open Label Brivaracetam Treatment
NCT00357669PHASE3COMPLETEDBrivaracetam as add-on Treatment of Unverricht-Lundborg Disease in Adolescents and Adults
NCT00464269PHASE3COMPLETEDDouble-blind, Randomized Study Evaluating the Efficacy and Safety of Brivaracetam in Adults With Partial Onset Seizures
NCT00490035PHASE3COMPLETEDDouble-blind, Randomized Study Evaluating the Efficacy and Safety of Brivaracetam in Adults With Partial Onset Seizures
NCT00504881PHASE3COMPLETEDBrivaracetam as add-on Treatment in Adolescents and Adults Suffering From Epilepsy
NCT00698581PHASE3TERMINATEDA Double-blind, Randomized Conversion to Monotherapy Study to Evaluate the Efficacy and Safety of Brivaracetam in Subjects (≥ 16 to 75 Years Old) With Partial Onset Seizures
NCT00699283PHASE3TERMINATEDA Double-blind, Randomized Conversion to Monotherapy Study to Evaluate the Efficacy and Safety of Brivaracetam in Subjects (≥ 16 to 75 Years Old) With Partial Onset Seizures
NCT00761774PHASE3COMPLETEDAn Open-label, Multinational, Multicenter, Follow-up Study to Evaluate the Long-term Safety and Efficacy of Brivaracetam
NCT01261325PHASE3COMPLETEDBrivaracetam Efficacy and Safety Study in Subjects With Partial Onset Seizures
NCT01339559PHASE3COMPLETEDBrivaracetam Safety and Efficacy Follow-up Study in Subjects With Epilepsy
NCT01364597PHASE3COMPLETEDOpen-label Long-term Study of Adjunctive Brivaracetam in Pediatric Subjects With Epilepsy
NCT01405508PHASE3COMPLETEDSafety and Tolerability of Intravenous Brivaracetam (Infusion or Bolus) as Adjunctive Antiepileptic Therapy
NCT01653262PHASE3COMPLETEDEffect of Brivaracetam (BRV) on Nonpsychotic Behavioral Side Effects in Subjects Treated Previously With Levetiracetam (LEV)
NCT01728077PHASE3COMPLETEDEvaluation of Long-term Safety, and Efficacy of Brivaracetam (BRV) Used as Adjunctive Treatment in Subjects With Epilepsy
NCT03083665PHASE3COMPLETEDA Study to Evaluate the Efficacy and Safety of Brivaracetam in Study Participants (>=16 to 80 Years of Age) With Epilepsy
NCT03250377PHASE3COMPLETEDA Study to Test the Safety/ Efficacy of Brivaracetam (BRV) Used as Adjunctive Treatment in Subjects >=16 Years of Age With Partial Seizures With or Without Secondary Generalization
NCT03325439PHASE3TERMINATEDA Study to Test the Pharmacokinetics, Efficacy, and Safety of Brivaracetam in Newborns With Repeated Electroencephalographic Seizures
NCT03685630PHASE3COMPLETEDA Study to Evaluate the Safety and Tolerability of Intravenous Brivaracetam (BRV) as Replacement for Oral Brivaracetam in Japanese Subjects >=16 Years of Age With Partial Seizures With or Without Secondary Generalization
NCT05109234PHASE3COMPLETEDA Study to Test the Long-term Safety, Tolerability and Efficacy of Brivaracetam in Study Participants 2 to 26 Years of Age With Childhood Absence Epilepsy or Juvenile Absence Epilepsy
NCT05639946PHASE3COMPLETEDBrivaracetam to Reduce Neuropathic Pain in Chronic SCI: A Randomized, Double-Blind, Placebo-Controlled Clinical Trial
NCT07563634PHASE3COMPLETEDLong-term Safety and Efficacy of Adjunctive Brivaracetam in Chinese Patients With Uncontrolled Focal Epilepsy
NCT05899764PHASE1/PHASE2NOT_YET_RECRUITINGEpileptic Hippocampus in Alzheimer’s Disease
NCT00160667PHASE2COMPLETEDA Study Assessing Efficacy of Brivaracetam in Subjects With Persistent Pain After Shingles (Post-herpetic Neuralgia)
NCT00175825PHASE2COMPLETEDA Dose-ranging Study With Brivaracetam in Patients From 16 to 65 Years With Refractory Partial Onset Seizures.
NCT00175929PHASE2COMPLETEDA Study of Brivaracetam in Subjects With Partial Onset Seizures
NCT00401648PHASE2COMPLETEDEffect of Brivaracetam in Photosensitive Epileptic Subjects
NCT00422422PHASE2COMPLETEDOpen-label, Pharmacokinetic, Safety and Efficacy Study of Adjunctive Brivaracetam in Children With Epilepsy.
NCT02088957PHASE2TERMINATEDEfficacy Evaluation of Intravenous Brivaracetam and Phenytoin in Subjects With Nonconvulsive Electrographic Seizures
NCT03021018PHASE2COMPLETEDA Study to Assess the Efficacy and Safety of Brivaracetam as Treatment for Increased Seizure Activity in an Epilepsy Monitoring Unit Setting
NCT03405714PHASE2COMPLETEDA Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of Intravenous Brivaracetam in Subjects >= 1 Month to < 16 Years of Age With Epilepsy
NCT04379011PHASE1/PHASE2COMPLETEDBrivaracetam to Reduce Neuropathic Pain in Chronic Spinal Cord Injury
NCT00426673PHASE1COMPLETEDAn Open-Label Interaction Study to Look at the Effects of Brivaracetam on Phenytoin When Taken Together in 15 Adult Patients With Epilepsy.
NCT00736931PHASE1COMPLETEDClinical Study in Healthy Volunteers to Investigate the Neurocognitive Effects of a New Antiepileptic Drug: Brivaracetam
NCT01710670PHASE1COMPLETEDA Study to Investigate the Drug-Drug Interactions of Brivaracetam and Ethanol in Healthy Male Subjects
NCT02602860PHASE1COMPLETEDA Brain Imaging Study With Positron Emission Tomography and the Radiotracer [11C]UCB-J to Estimate How Fast Brivaracetam and Levetiracetam Enter the Brain in Healthy Volunteers
NCT03695094PHASE1COMPLETEDA Study in Participants With Epilepsy, to Evaluate the Pharmacokinetics, Safety and Tolerability of Oxcarbazepine on Padsevonil
NCT04882540PHASE1COMPLETEDA Study to Evaluate the Pharmacokinetics and Safety of Brivaracetam in Healthy Chinese Subjects

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No CPIC/DPWG dosing guideline, but PharmGKB curates 1 clinical and 1 variant annotation(s) for this drug (gene-keyed; see PharmGKB).

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).