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Dexmedetomidine administered intranasally

First Affiliated Hospital of Chongqing Medical University · Phase 3 active Small molecule

Dexmedetomidine is a selective alpha-2 adrenergic receptor agonist that produces sedation, analgesia, and anxiolysis by activating presynaptic and postsynaptic alpha-2 receptors in the central nervous system.

Dexmedetomidine is a selective alpha-2 adrenergic receptor agonist that produces sedation, analgesia, and anxiolysis by activating presynaptic and postsynaptic alpha-2 receptors in the central nervous system. Used for Procedural sedation via intranasal administration, Acute anxiety or agitation management.

At a glance

Generic nameDexmedetomidine administered intranasally
SponsorFirst Affiliated Hospital of Chongqing Medical University
Drug classAlpha-2 adrenergic receptor agonist
TargetAlpha-2 adrenergic receptor
ModalitySmall molecule
Therapeutic areaAnesthesia/Sedation
PhasePhase 3

Mechanism of action

Dexmedetomidine binds with high selectivity to alpha-2 adrenergic receptors, which are distributed throughout the brain and spinal cord. This activation leads to decreased norepinephrine release and reduced neuronal firing, resulting in sedative and analgesic effects. The intranasal route provides non-invasive delivery for rapid onset of action, potentially useful for procedural sedation or acute anxiety management.

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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