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Suzetrigine in moderate to severe acute pain: a profile of its use

Aisling McGuigan, Matt Shirley

Drugs & therapy perspectives, 2026

1 citation

Abstract

Suzetrigine (JOURNAVX™), a first-in-class voltage-gated sodium channel 1.8 (NaV1.8) inhibitor, is an efficacious and well-tolerated non-opioid analgesic approved in the USA for the treatment of moderate to severe acute pain in adults. By selectively inhibiting the peripherally restricted NaV1.8 to reduce pain signal transmission, suzetrigine is expected to have minimal addictive potential. As shown in two double-blind, placebo- and active-controlled phase 3 trials in adults experiencing moderate to severe acute pain following a bunionectomy or abdominoplasty, a 48-h course of oral suzetrigine reduces pain intensity significantly more than placebo, although the trials did not demonstrate the superiority of suzetrigine over the opioid-based active comparator, hydrocodone bitartrate/acetaminophen 5 mg/325 mg. Suzetrigine is generally well tolerated; in clinical trials, nausea, constipation, and headache were the most common adverse events and most were of mild or moderate severity. No evidence of addictive potential for suzetrigine was found based on in vitro, preclinical, and clinical trial data. Pain is an unpleasant and emotional experience resulting from actual or potential tissue damage that is described as acute when it is sudden onset and lasts for ≤ 30 days. Sequelae from inadequately treated moderate to severe acute pain can be a substantial burden on patients, their families, healthcare systems, and society. Current treatment options for moderate to severe acute pain…

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