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IV dexmedetomidine

The University of Hong Kong · 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 Sedation in intensive care unit patients, Perioperative sedation and analgesia, Procedural sedation.

At a glance

Generic nameIV dexmedetomidine
SponsorThe University of Hong Kong
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 drug produces a unique sedation profile characterized by maintained airway reflexes and the ability to be aroused, distinguishing it from other sedatives.

Approved indications

Common side effects

Key clinical trials

Primary sources

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