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

Drugs

EvaluationDrugModalityDoseRoute
Subject Suzetrigine Small molecule Oral

Indications