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NCT06972212

Pharmacodynamic Study of 100mg Suzegtrigine vs Placebo in Healthy Male Adults

Completed EARLY_PHASE1 Last updated 3 July 2025
What this trial tests

EARLY_PHASE1 trial testing suzetrigine 100mg in Pain Detection in 20 participants. Completed in 28 June 2025.

Timeline
4 June 2025
Primary endpoint
28 June 2025
28 June 2025

Quick facts

Lead sponsorLatigo Biotherapeutics
PhaseEARLY_PHASE1
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingtriple
Primary purposetreatment
Enrollment20
Start date4 June 2025
Primary completion28 June 2025
Estimated completion28 June 2025
Sites1 location across New Zealand

Drugs / interventions tested

Conditions studied

Sponsor

Latigo Biotherapeutics — full company profile →

Who can join

Adults 18 to 55, male only, with Pain Detection or Pain Threshold. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a randomized, double-blind, placebo-controlled within-participant crossover study in healthy male participants 18-55 years of age to assess pain tolerance during a cold pressor test. The study will be conducted at a single center in New Zealand.

Publications & conference data

2 peer-reviewed publications reference this trial (live from Europe PMC):

  1. Suzetrigine, a Non-Opioid Small-Molecule Analgesic: Mechanism of Action, Clinical, and Translational Science.
    Rajasingham R, Qi Y. · · 2025 · cited 3× · PMID 41251403 · DOI 10.1111/cts.70414
  2. Suzetrigine, a Na<sub>V</sub>1.8 Inhibitor as a Novel Approach for Pain Therapy-A Medicinal and Chemical Drug Profile.
    Medhat RM, Kotb OA, Baecker D. · · 2026 · cited 1× · PMID 41599406 · DOI 10.3390/molecules31020358

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Other Latigo Biotherapeutics trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06972212.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing