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Lexapro (escitalopram)

St. Luke's-Roosevelt Hospital Center · FDA-approved active Small molecule

Lexapro (escitalopram) is a Selective serotonin reuptake inhibitor (SSRI) Small molecule drug developed by St. Luke's-Roosevelt Hospital Center. It is currently FDA-approved for Major depressive disorder, Generalized anxiety disorder, Panic disorder. Also known as: lexapro, escitalopram, s-citalopram, d-citalopram.

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

Escitalopram 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 nameLexapro (escitalopram)
Also known aslexapro, escitalopram, s-citalopram, d-citalopram
SponsorSt. Luke's-Roosevelt Hospital Center
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 protein, it prevents the reabsorption of serotonin from the synaptic cleft back into the presynaptic neuron, 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

Competitive intelligence

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Frequently asked questions about Lexapro (escitalopram)

What is Lexapro (escitalopram)?

Lexapro (escitalopram) is a Selective serotonin reuptake inhibitor (SSRI) drug developed by St. Luke's-Roosevelt Hospital Center, indicated for Major depressive disorder, Generalized anxiety disorder, Panic disorder.

How does Lexapro (escitalopram) work?

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

What is Lexapro (escitalopram) used for?

Lexapro (escitalopram) is indicated for Major depressive disorder, Generalized anxiety disorder, Panic disorder, Social anxiety disorder, Obsessive-compulsive disorder.

Who makes Lexapro (escitalopram)?

Lexapro (escitalopram) is developed and marketed by St. Luke's-Roosevelt Hospital Center (see full St. Luke's-Roosevelt Hospital Center pipeline at /company/st-luke-s-roosevelt-hospital-center).

Is Lexapro (escitalopram) also known as anything else?

Lexapro (escitalopram) is also known as lexapro, escitalopram, s-citalopram, d-citalopram.

What drug class is Lexapro (escitalopram) in?

Lexapro (escitalopram) belongs to the Selective serotonin reuptake inhibitor (SSRI) class. See all Selective serotonin reuptake inhibitor (SSRI) drugs at /class/selective-serotonin-reuptake-inhibitor-ssri.

What development phase is Lexapro (escitalopram) in?

Lexapro (escitalopram) is FDA-approved (marketed).

What are the side effects of Lexapro (escitalopram)?

Common side effects of Lexapro (escitalopram) include Nausea, Headache, Insomnia, Somnolence, Sexual dysfunction, Diarrhea.

What does Lexapro (escitalopram) target?

Lexapro (escitalopram) targets Serotonin transporter (SERT) and is a Selective serotonin reuptake inhibitor (SSRI).

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