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Oral ivermectin

University of Oxford · FDA-approved active Small molecule

Ivermectin binds to glutamate-gated chloride channels in parasitic organisms, causing paralysis and death of the parasite.

Ivermectin binds to glutamate-gated chloride channels in parasites, causing paralysis and death of susceptible organisms. Used for Onchocerciasis (river blindness), Lymphatic filariasis, Strongyloidiasis.

At a glance

Generic nameOral ivermectin
Also known asNT007, Liconsa Laboratorios, ivermectin, Direct antiviarl agents
SponsorUniversity of Oxford
Drug classMacrocyclic lactone antiparasitic
TargetGlutamate-gated chloride channels (GluCl)
ModalitySmall molecule
Therapeutic areaInfectious Disease / Parasitology
PhaseFDA-approved

Mechanism of action

Ivermectin is an antiparasitic agent that selectively binds to invertebrate-specific glutamate-gated chloride ion channels, increasing chloride conductance and hyperpolarizing the cell membrane. This leads to paralysis and death of susceptible parasites. It has high selectivity for parasitic channels over mammalian GABA receptors, making it relatively safe for human use.

Approved indications

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

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

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