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Evaluation of Efficacy and Safety of Suzetrigine (SUZ) for Pain Associated With Diabetic Peripheral Neuropathy

← catalyst calendar

NCT07231419 · readout in 229 d

Sponsored by Vertex Pharmaceuticals Incorporated (industry) · VRTX — their whole pipeline →.

Phase
Phase 3
Status
Recruiting
Study type
Interventional
Design
Randomized · Quadruple · Treatment
Enrollment
734estimated
Sites
75
Country
United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2025-11-21actualWhen the study began enrolling
Primary completion2027-04-06estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2027-04-06estimatedThe whole study's end, after follow-up
First posted2025-11-17actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-07-20actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Diabetic Peripheral Neuropathic Pain

Interventions

  • Drug: Suzetrigine — also filed as VX-548, SUZ
  • Drug: Placebo (matched to SUZ)

Primary outcome

what the primary-completion date above is the date OF
Change From Baseline in the Weekly Average of Daily Pain Intensity on the Numeric Pain Rating Scale (NPRS) at Week 12 Compared to Placebo
measured From Baseline up to Week 12

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