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Keppra (levetiracetam)

Generic (originally UCB Pharma) · FDA-approved approved Small molecule Under review Quality 10/100

Keppra (generic name: levetiracetam) is a Antiepileptic agent Small molecule drug developed by Generic (originally UCB Pharma). It is currently FDA-approved (first approved 1999) for Epilepsy characterized by intractable complex partial seizures, Myoclonic Epilepsy Adjunct Treatment, Partial Epilepsy Treatment Adjunct. Also known as: Keppra, Keppra XR.

Levetiracetam binds to synaptic vesicle protein SV2A, potentially regulating vesicle exocytosis.

Keppra, also known as levetiracetam, is an anti-seizure medication used to treat partial-onset, myoclonic, or tonic-clonic seizures. It works by modulating the synaptic vesicle glycoprotein 2A, a small molecule mechanism that affects the release of neurotransmitters.

At a glance

Generic namelevetiracetam
Also known asKeppra, Keppra XR
SponsorGeneric (originally UCB Pharma)
Drug classAntiepileptic agent
TargetSynaptic vesicle protein SV2A
ModalitySmall molecule
Therapeutic areaMetabolic
PhaseFDA-approved
First approval1999-11-30 (United States)

Mechanism of action

The precise mechanism of levetiracetam's antiepileptic effect is unknown. A saturable and stereoselective neuronal binding site has been identified in rat brain tissue as the synaptic vesicle protein SV2A, which is thought to be involved in the regulation of vesicle exocytosis. Although the molecular significance of levetiracetam binding to SV2A is not fully understood, experimental data demonstrate that levetiracetam and related analogs show a rank order of affinity for SV2A that correlates with the potency of their antiseizure activity in audiogenic seizure-prone mice, suggesting that this interaction may contribute to the drug's antiepileptic mechanism of action.

Approved indications

Common side effects

Key clinical trials

Patents

PatentExpiryType
93394892034-03-14Formulation
96690092034-03-14Method of Use
78581222028-09-17Formulation
85357172026-02-22Formulation
81633062027-09-03Formulation
111607862034-03-14Formulation
88021422031-06-07Formulation
84259382026-02-22Formulation

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
FDA labelMechanism, indications, dosing, boxed warnings, drug interactions
ClinicalTrials.govTrial enrolment, design, endpoints, results
FDA Orange BookPatents + exclusivity

Competitive intelligence

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Frequently asked questions about Keppra

What is Keppra?

Keppra (levetiracetam) is a Antiepileptic agent drug developed by Generic (originally UCB Pharma), indicated for Epilepsy characterized by intractable complex partial seizures, Myoclonic Epilepsy Adjunct Treatment, Partial Epilepsy Treatment Adjunct.

How does Keppra work?

Levetiracetam binds to synaptic vesicle protein SV2A, potentially regulating vesicle exocytosis.

What is Keppra used for?

Keppra is indicated for Epilepsy characterized by intractable complex partial seizures, Myoclonic Epilepsy Adjunct Treatment, Partial Epilepsy Treatment Adjunct, Simple partial seizure, Status epilepticus.

Who makes Keppra?

Keppra is developed and marketed by Generic (originally UCB Pharma) (see full Generic (originally UCB Pharma) pipeline at /company/unknown).

What is the generic name of Keppra?

levetiracetam is the generic (nonproprietary) name of Keppra.

Is Keppra also known as anything else?

Keppra is also known as Keppra, Keppra XR.

What drug class is Keppra in?

Keppra belongs to the Antiepileptic agent class. See all Antiepileptic agent drugs at /class/antiepileptic-agent.

When was Keppra approved?

Keppra was first approved on 1999-11-30 in United States.

What development phase is Keppra in?

Keppra is FDA-approved (marketed).

What are the side effects of Keppra?

Common side effects of Keppra include Anemia, Lymphocyte count decreased, Neutrophil count decreased, Platelet count decreased, White blood cell decreased, Febrile neutropenia.

What does Keppra target?

Keppra targets Synaptic vesicle protein SV2A and is a Antiepileptic agent.

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing