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Cipralex (escitalopram)

Medical University of Vienna · FDA-approved active Small molecule

Cipralex selectively inhibits the reuptake of serotonin at the neuronal synapse, increasing serotonin availability in the brain.

Cipralex selectively inhibits the reuptake of serotonin at the neuronal synapse, increasing serotonin availability in the brain. Used for Major depressive disorder, Generalized anxiety disorder, Panic disorder.

At a glance

Generic nameCipralex (escitalopram)
SponsorMedical University of Vienna
Drug classSelective serotonin reuptake inhibitor (SSRI)
TargetSerotonin transporter (SERT)
ModalitySmall molecule
Therapeutic areaPsychiatry / Mental Health
PhaseFDA-approved

Mechanism of action

Escitalopram is the active S-enantiomer of citalopram and works as a selective serotonin reuptake inhibitor (SSRI). By blocking the serotonin transporter (SERT) on presynaptic neurons, it prevents the reabsorption of serotonin from the synaptic cleft, thereby increasing serotonin concentration and enhancing neurotransmission. This mechanism is thought to improve mood and reduce anxiety symptoms in depression and anxiety disorders.

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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