drugset / Trial / NCT06176196

Evaluation of Efficacy and Safety of VX-548 for Painful Lumbosacral Radiculopathy (PLSR)

NCT06176196 ↗

Phase 2 Completed 218 enrolled Vertex Pharmaceuticals Incorporated
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of the study is to evaluate the efficacy and safety of VX-548 in treating participants with PLSR.

Timeline

Start
2023-12-13
Primary completion
2024-10-02
Completion
2024-10-16

Outcome

Met primary endpoint

release “in people with painful lumbosacral radiculopathy (LSR). The study met its primary endpoint” vrtx.com ↗

release “suzetrigine in painful lumbosacral radiculopathy (LSR), a form of peripheral neuropathic pain. The study met its primary endpoint” vrtx.com ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Suzetrigine Small molecule — Oral

Indications