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transdermal clonidine

Peking University People's Hospital · FDA-approved active Small molecule

Transdermal clonidine is an alpha-2 adrenergic agonist that reduces sympathetic nervous system activity, lowering blood pressure and heart rate.

Transdermal clonidine is an alpha-2 adrenergic agonist that reduces sympathetic nervous system activity, lowering blood pressure and heart rate. Used for Hypertension, Attention-deficit/hyperactivity disorder (ADHD).

At a glance

Generic nametransdermal clonidine
SponsorPeking University People's Hospital
Drug classAlpha-2 adrenergic agonist
TargetAlpha-2 adrenergic receptor
ModalitySmall molecule
Therapeutic areaCardiovascular
PhaseFDA-approved

Mechanism of action

Clonidine binds to alpha-2 adrenergic receptors in the central nervous system, decreasing the release of norepinephrine and reducing sympathetic outflow. The transdermal formulation provides sustained drug delivery through the skin, maintaining therapeutic levels over extended periods. This mechanism results in vasodilation and reduced cardiac output, leading to antihypertensive effects.

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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