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modafinil (M1, M2, M4)

University of California, Los Angeles · FDA-approved active Small molecule

Modafinil promotes wakefulness by increasing dopamine and norepinephrine activity in the brain, particularly in the hypothalamus and prefrontal cortex.

Modafinil promotes wakefulness by increasing dopamine and norepinephrine activity in the brain, particularly in the hypothalamus and prefrontal cortex. Used for Narcolepsy, Obstructive sleep apnea (OSA)-associated excessive daytime sleepiness, Shift work sleep disorder.

At a glance

Generic namemodafinil (M1, M2, M4)
Also known asProvigil
SponsorUniversity of California, Los Angeles
Drug classEugeroic (wakefulness-promoting agent)
TargetDopamine transporter (DAT); norepinephrine transporter (NET); orexin system modulation
ModalitySmall molecule
Therapeutic areaNeurology / Sleep Medicine
PhaseFDA-approved

Mechanism of action

Modafinil is a eugeroic (wakefulness-promoting) agent that works through multiple mechanisms including inhibition of dopamine reuptake, enhancement of noradrenergic signaling, and modulation of orexin/hypocretin neurons. The exact mechanism is not fully elucidated, but it does not act as a traditional stimulant like amphetamines. It selectively enhances alertness and cognitive function while maintaining a lower abuse potential than classical stimulants.

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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