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The Role of NaV1.8 in Human Pain Models

This study aims to understand how NaV1.8, a specific type of sodium channel found in peripheral nerves, contributes to different types of pain in humans. To address this, suzetrigine, a highly selective blocker of the NaV1.8 channel, is used. While current pain medications often have side effects that limit their use,

Condition(s)Pain, Acute Pain, Healthy Volunteer Study
StatusRecruiting
PhaseEARLY_Phase 1
Study typeInterventional
SummaryThis study aims to understand how NaV1.8, a specific type of sodium channel found in peripheral nerves, contributes to different types of pain in humans. To address this, suzetrigine, a highly selective blocker of the NaV1.8 channel, is used. While current pain medications often have side effects that limit their use, NaV1.8 is a promising target for new, non-opioid pain treatments because it is primarily located in the nerves that send pain signals to the brain. This study is a randomised, placebo-controlled double-blind crossover microdosing trial. This means that very small, safe amounts of the drug are injected directly into the skin of healthy volunteers to observe its effects locally. This approach ensures the drug works only at the injection site with negligible exposure to the rest
Who can participateInclusion criteria * Age between 18 and 70 years * Full legal capacity Exclusion criteria * Participant of another study, ongoing or within the last 4 weeks * Medication intake (except contraception) or drug abuse * Female subjects: Positive pregnancy test or breastfeeding * Verified body temperature above 38°C * Known allergic diseases, in particular asthmatic disorders * Limited accessibility of forearms (e.g. orthopedic cast) * Sensory deficit, skin disease or hematoma at the forarms
Ages18 Years to 70 Years
SexAll
Accepts healthy volunteersYes
Lead sponsorMedical University of Vienna
LocationsVienna, State of Vienna, Austria
Start date2026-04-21
NCT IDNCT07511400
Official listinghttps://clinicaltrials.gov/study/NCT07511400

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