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Lacosamide - rapid titration 2

Seoul National University Hospital · FDA-approved active Small molecule

Lacosamide enhances slow inactivation of voltage-gated sodium channels, thereby stabilizing neuronal membranes and reducing seizure activity.

Lacosamide enhances slow inactivation of voltage-gated sodium channels, thereby stabilizing neuronal membranes and reducing seizure activity. Used for Partial-onset seizures (adjunctive therapy), Diabetic neuropathic pain.

At a glance

Generic nameLacosamide - rapid titration 2
SponsorSeoul National University Hospital
Drug classAnticonvulsant; sodium channel modulator
TargetVoltage-gated sodium channels; CRMP-2
ModalitySmall molecule
Therapeutic areaNeurology
PhaseFDA-approved

Mechanism of action

Lacosamide is a functionalized amino acid that selectively enhances slow inactivation of voltage-gated sodium channels, which reduces repetitive neuronal firing and prevents seizure propagation. This mechanism differs from traditional sodium channel blockers by preferentially affecting the slow inactivation phase rather than fast inactivation. The drug also has activity at collapsin response mediator protein 2 (CRMP-2), which may contribute to its anticonvulsant effects.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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