<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>142(6)</volume><submitter>Bertoch T</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Opioids are effective for treating acute pain but have safety, tolerability, and addiction concerns while nonopioid analgesics have limited efficacy. Suzetrigine, an oral, nonopioid small molecule, selectively inhibits the voltage-gated sodium channel 1.8 (NaV1.8) and has potential to provide efficacious and safe relief for acute pain without addiction concerns.&lt;h4>Methods&lt;/h4>To evaluate suzetrigine for treatment of acute pain, two phase 3, randomized, double-blind, placebo- and active-controlled trials were conducted in adults with moderate-to-severe acute pain on the verbal categorical rating scale and 4 or greater on the numeric pain rating scale after abdominoplasty (n = 1,118) or bunionectomy (n = 1,073). After surgery, participants were randomized to suzetrigine (</pubmed_abstract><journal>Anesthesiology</journal><pagination>1085-1099</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12061372</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Suzetrigine, a Nonopioid Na V 1.8 Inhibitor for Treatment of Moderate-to-severe Acute Pain: Two Phase 3 Randomized Clinical Trials.</pubmed_title><pmcid>PMC12061372</pmcid><pubmed_authors>Swisher MW</pubmed_authors><pubmed_authors>Correll DJ</pubmed_authors><pubmed_authors>D'Aunno D</pubmed_authors><pubmed_authors>Solanki D</pubmed_authors><pubmed_authors>Bozic C</pubmed_authors><pubmed_authors>Taber L</pubmed_authors><pubmed_authors>Weiner SG</pubmed_authors><pubmed_authors>McCoun J</pubmed_authors><pubmed_authors>Negulescu P</pubmed_authors><pubmed_authors>Urban J</pubmed_authors><pubmed_authors>Oswald J</pubmed_authors><pubmed_authors>Miao X</pubmed_authors><pubmed_authors>Tian S</pubmed_authors><pubmed_authors>Bertoch T</pubmed_authors></additional><is_claimable>false</is_claimable><name>Suzetrigine, a Nonopioid Na V 1.8 Inhibitor for Treatment of Moderate-to-severe Acute Pain: Two Phase 3 Randomized Clinical Trials.</name><description>&lt;h4>Background&lt;/h4>Opioids are effective for treating acute pain but have safety, tolerability, and addiction concerns while nonopioid analgesics have limited efficacy. Suzetrigine, an oral, nonopioid small molecule, selectively inhibits the voltage-gated sodium channel 1.8 (NaV1.8) and has potential to provide efficacious and safe relief for acute pain without addiction concerns.&lt;h4>Methods&lt;/h4>To evaluate suzetrigine for treatment of acute pain, two phase 3, randomized, double-blind, placebo- and active-controlled trials were conducted in adults with moderate-to-severe acute pain on the verbal categorical rating scale and 4 or greater on the numeric pain rating scale after abdominoplasty (n = 1,118) or bunionectomy (n = 1,073). After surgery, participants were randomized to suzetrigine (</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jun</publication><modification>2026-06-02T17:56:57.877Z</modification><creation>2026-04-18T03:11:59.261Z</creation></dates><accession>S-EPMC12061372</accession><cross_references><pubmed>40117446</pubmed><doi>10.1097/ALN.0000000000005460</doi></cross_references></HashMap>