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Citalopram HCl

Universitaire Ziekenhuizen KU Leuven · FDA-approved active Small molecule

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

Citalopram selectively inhibits the reuptake of serotonin at the neuronal synapse, increasing serotonin availability in the brain. Used for Major depressive disorder, Panic disorder, Obsessive-compulsive disorder.

At a glance

Generic nameCitalopram HCl
SponsorUniversitaire Ziekenhuizen KU Leuven
Drug classSelective serotonin reuptake inhibitor (SSRI)
TargetSerotonin transporter (SERT)
ModalitySmall molecule
Therapeutic areaPsychiatry / Mental Health
PhaseFDA-approved

Mechanism of action

Citalopram is a selective serotonin reuptake inhibitor (SSRI) that blocks the serotonin transporter protein, preventing the reabsorption of serotonin from the synaptic cleft back into presynaptic neurons. This increases serotonin concentration in the extracellular space, enhancing serotonergic neurotransmission. The enhanced serotonin signaling is thought to improve mood and alleviate symptoms of 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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