Brivaracetam
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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
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL607400 |
| Name | Brivaracetam |
| Type | Small molecule |
| Max phase | 4 |
| FDA approved | yes |
| PubChem CID | 9837243 |
| ChEBI | CHEBI:133013 |
| ATC | N03AX23 |
| Molecular formula | C11H20N2O2 |
| Molecular weight | 212.29 |
| InChIKey | MSYKRHVOOPPJKU-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).
| Gene | Target | Action | pAffinity | Cancer dependency | UniProt |
|---|---|---|---|---|---|
| SV2A | synaptic vesicle glycoprotein 2A | Inhibition | 7 | 5.6% | 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:
| Pathway | Targets | Genes |
|---|---|---|
| Disease | 1 | SV2A |
| Neurotoxicity of clostridium toxins | 1 | SV2A |
| Toxicity of botulinum toxin type D (botD) | 1 | SV2A |
| Toxicity of botulinum toxin type A (botA) | 1 | SV2A |
| Toxicity of botulinum toxin type F (botF) | 1 | SV2A |
| Toxicity of botulinum toxin type E (botE) | 1 | SV2A |
| Uptake and actions of bacterial toxins | 1 | SV2A |
| Infectious disease | 1 | SV2A |
| Bacterial Infection Pathways | 1 | SV2A |
Dominant GO biological processes
| GO term | Targets |
|---|---|
| intracellular calcium ion homeostasis | 1 |
| synaptic vesicle priming | 1 |
| neurotransmitter transport | 1 |
| chemical synaptic transmission | 1 |
| transmembrane transport | 1 |
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).
| Indication | Trial phase | MONDO | EFO |
|---|---|---|---|
| epilepsy | 4 | MONDO:0005027 | EFO:0000474 |
| visual epilepsy | 4 | MONDO:0001386 | HP:0001250 |
| Unverricht-Lundborg syndrome | 3 | MONDO:0009698 | Orphanet:308 |
| spinal cord injury | 1 | MONDO:0043797 | EFO:1001919 |
| brain neoplasm | 0 | MONDO:0021211 | EFO: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
| Phase | Trials |
|---|---|
| PHASE3 | 24 |
| PHASE2 | 8 |
| PHASE1 | 8 |
| Not specified | 5 |
| PHASE1/PHASE2 | 2 |
| EARLY_PHASE1 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT04666610 | PHASE3 | ACTIVE_NOT_RECRUITING | A 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 |
| NCT04715646 | PHASE3 | RECRUITING | A Study to Test the Safety and Tolerability of Brivaracetam in Children and Adolescents With Seizures |
| NCT06315322 | PHASE3 | RECRUITING | A Study to Test the Long-term Safety and Tolerability of Brivaracetam in Study Participants With Childhood Absence Epilepsy or Juvenile Absence Epilepsy |
| NCT00150800 | PHASE3 | COMPLETED | This 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 |
| NCT00357669 | PHASE3 | COMPLETED | Brivaracetam as add-on Treatment of Unverricht-Lundborg Disease in Adolescents and Adults |
| NCT00464269 | PHASE3 | COMPLETED | Double-blind, Randomized Study Evaluating the Efficacy and Safety of Brivaracetam in Adults With Partial Onset Seizures |
| NCT00490035 | PHASE3 | COMPLETED | Double-blind, Randomized Study Evaluating the Efficacy and Safety of Brivaracetam in Adults With Partial Onset Seizures |
| NCT00504881 | PHASE3 | COMPLETED | Brivaracetam as add-on Treatment in Adolescents and Adults Suffering From Epilepsy |
| NCT00698581 | PHASE3 | TERMINATED | A 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 |
| NCT00699283 | PHASE3 | TERMINATED | A 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 |
| NCT00761774 | PHASE3 | COMPLETED | An Open-label, Multinational, Multicenter, Follow-up Study to Evaluate the Long-term Safety and Efficacy of Brivaracetam |
| NCT01261325 | PHASE3 | COMPLETED | Brivaracetam Efficacy and Safety Study in Subjects With Partial Onset Seizures |
| NCT01339559 | PHASE3 | COMPLETED | Brivaracetam Safety and Efficacy Follow-up Study in Subjects With Epilepsy |
| NCT01364597 | PHASE3 | COMPLETED | Open-label Long-term Study of Adjunctive Brivaracetam in Pediatric Subjects With Epilepsy |
| NCT01405508 | PHASE3 | COMPLETED | Safety and Tolerability of Intravenous Brivaracetam (Infusion or Bolus) as Adjunctive Antiepileptic Therapy |
| NCT01653262 | PHASE3 | COMPLETED | Effect of Brivaracetam (BRV) on Nonpsychotic Behavioral Side Effects in Subjects Treated Previously With Levetiracetam (LEV) |
| NCT01728077 | PHASE3 | COMPLETED | Evaluation of Long-term Safety, and Efficacy of Brivaracetam (BRV) Used as Adjunctive Treatment in Subjects With Epilepsy |
| NCT03083665 | PHASE3 | COMPLETED | A Study to Evaluate the Efficacy and Safety of Brivaracetam in Study Participants (>=16 to 80 Years of Age) With Epilepsy |
| NCT03250377 | PHASE3 | COMPLETED | A 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 |
| NCT03325439 | PHASE3 | TERMINATED | A Study to Test the Pharmacokinetics, Efficacy, and Safety of Brivaracetam in Newborns With Repeated Electroencephalographic Seizures |
| NCT03685630 | PHASE3 | COMPLETED | A 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 |
| NCT05109234 | PHASE3 | COMPLETED | A 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 |
| NCT05639946 | PHASE3 | COMPLETED | Brivaracetam to Reduce Neuropathic Pain in Chronic SCI: A Randomized, Double-Blind, Placebo-Controlled Clinical Trial |
| NCT07563634 | PHASE3 | COMPLETED | Long-term Safety and Efficacy of Adjunctive Brivaracetam in Chinese Patients With Uncontrolled Focal Epilepsy |
| NCT05899764 | PHASE1/PHASE2 | NOT_YET_RECRUITING | Epileptic Hippocampus in Alzheimer’s Disease |
| NCT00160667 | PHASE2 | COMPLETED | A Study Assessing Efficacy of Brivaracetam in Subjects With Persistent Pain After Shingles (Post-herpetic Neuralgia) |
| NCT00175825 | PHASE2 | COMPLETED | A Dose-ranging Study With Brivaracetam in Patients From 16 to 65 Years With Refractory Partial Onset Seizures. |
| NCT00175929 | PHASE2 | COMPLETED | A Study of Brivaracetam in Subjects With Partial Onset Seizures |
| NCT00401648 | PHASE2 | COMPLETED | Effect of Brivaracetam in Photosensitive Epileptic Subjects |
| NCT00422422 | PHASE2 | COMPLETED | Open-label, Pharmacokinetic, Safety and Efficacy Study of Adjunctive Brivaracetam in Children With Epilepsy. |
| NCT02088957 | PHASE2 | TERMINATED | Efficacy Evaluation of Intravenous Brivaracetam and Phenytoin in Subjects With Nonconvulsive Electrographic Seizures |
| NCT03021018 | PHASE2 | COMPLETED | A Study to Assess the Efficacy and Safety of Brivaracetam as Treatment for Increased Seizure Activity in an Epilepsy Monitoring Unit Setting |
| NCT03405714 | PHASE2 | COMPLETED | A Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of Intravenous Brivaracetam in Subjects >= 1 Month to < 16 Years of Age With Epilepsy |
| NCT04379011 | PHASE1/PHASE2 | COMPLETED | Brivaracetam to Reduce Neuropathic Pain in Chronic Spinal Cord Injury |
| NCT00426673 | PHASE1 | COMPLETED | An Open-Label Interaction Study to Look at the Effects of Brivaracetam on Phenytoin When Taken Together in 15 Adult Patients With Epilepsy. |
| NCT00736931 | PHASE1 | COMPLETED | Clinical Study in Healthy Volunteers to Investigate the Neurocognitive Effects of a New Antiepileptic Drug: Brivaracetam |
| NCT01710670 | PHASE1 | COMPLETED | A Study to Investigate the Drug-Drug Interactions of Brivaracetam and Ethanol in Healthy Male Subjects |
| NCT02602860 | PHASE1 | COMPLETED | A 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 |
| NCT03695094 | PHASE1 | COMPLETED | A Study in Participants With Epilepsy, to Evaluate the Pharmacokinetics, Safety and Tolerability of Oxcarbazepine on Padsevonil |
| NCT04882540 | PHASE1 | COMPLETED | A 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).
Related molecules
Related molecules
No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).
Related Atlas pages
- Genes: SV2A
- Diseases: epilepsy, Unverricht-Lundborg syndrome