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Transdermal Methylphenidate

St. Louis University · FDA-approved active Small molecule

Transdermal methylphenidate is a central nervous system stimulant that increases dopamine and norepinephrine availability in the brain by inhibiting their reuptake.

Transdermal methylphenidate is a central nervous system stimulant that increases dopamine and norepinephrine availability in the brain by inhibiting their reuptake. Used for Attention-deficit/hyperactivity disorder (ADHD), Narcolepsy.

At a glance

Generic nameTransdermal Methylphenidate
Also known asDaytrana
SponsorSt. Louis University
Drug classSympathomimetic amine; central nervous system stimulant
TargetDopamine transporter (DAT); norepinephrine transporter (NET)
ModalitySmall molecule
Therapeutic areaNeurology; Psychiatry
PhaseFDA-approved

Mechanism of action

Methylphenidate blocks the reuptake of dopamine and norepinephrine at the presynaptic neuron, leading to increased concentrations of these neurotransmitters in the synaptic cleft. The transdermal formulation delivers the drug through the skin, providing sustained release over 9 hours and avoiding first-pass hepatic metabolism. This mechanism enhances attention, focus, and wakefulness, making it effective for attention-deficit/hyperactivity disorder and narcolepsy.

Approved indications

Common side effects

Key clinical trials

Primary sources

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