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Lucemyra (LOFEXIDINE)

Biocorrx Pharms · FDA-approved approved Small molecule

Lucemyra works by activating the alpha-2A adrenergic receptor to reduce the release of norepinephrine, a neurotransmitter involved in withdrawal symptoms.

Lucemyra (lofexidine) is a small molecule drug that targets the alpha-2A adrenergic receptor to treat opioid withdrawal. It was originally developed by US WorldMeds LLC and is now owned by Biocorrx Pharmaceuticals. Lucemyra was FDA-approved in 2018 for the management of opioid withdrawal symptoms. The drug has a half-life of 12 hours and high bioavailability of 90%. It is now off-patent with multiple generic manufacturers.

At a glance

Generic nameLOFEXIDINE
SponsorBiocorrx Pharms
Drug classlofexidine
TargetAlpha-2A adrenergic receptor
ModalitySmall molecule
Therapeutic areaNeuroscience
PhaseFDA-approved
First approval2018

Mechanism of action

Lofexidine is central alpha-2 adrenergic agonist that binds to receptors on adrenergic neurons. This reduces the release of norepinephrine and decreases sympathetic tone.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
FDA labelMechanism, indications, dosing, boxed warnings, drug interactions
ClinicalTrials.govTrial enrolment, design, endpoints, results

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