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valproic acid (VPA)

Hospital Universitari de Bellvitge · Phase 3 active Small molecule

Valproic acid acts as a sodium channel blocker and inhibits the release of excitatory neurotransmitters.

Valproic acid acts as a sodium channel blocker and inhibits the release of excitatory neurotransmitters. Used for Seizure prevention in epilepsy, Mood stabilization in bipolar disorder.

At a glance

Generic namevalproic acid (VPA)
Also known asValrpoic acid, Phenytoin, Benzodiazepines, Status Epilepticus Refractarius, Depakene
SponsorHospital Universitari de Bellvitge
Drug classAnticonvulsant
TargetVoltage-gated sodium channels
ModalitySmall molecule
Therapeutic areaNeurology
PhasePhase 3

Mechanism of action

Valproic acid's mechanism of action is primarily through the blockade of voltage-gated sodium channels, which reduces the release of excitatory neurotransmitters such as glutamate. This leads to a decrease in neuronal excitability and a subsequent reduction in seizure activity. Additionally, valproic acid has been shown to have a stabilizing effect on neuronal membranes, further contributing to its anticonvulsant properties.

Approved indications

Common side effects

Key clinical trials

Primary sources

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