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Study identifier: NCT06176196 Synced from ClinicalTrials.gov · August 07, 2026
● Study status: Completed

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

Condition: Painful Lumbosacral Radiculopathy  ·  Sponsor: Vertex Pharmaceuticals Incorporated

PhasePhase 2
Planned participants218
Who can joinAll sexes, 18 Years to 70 Years
Healthy volunteersNo

Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.

About this study

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

This description comes directly from the study's public registry record.

Talk to the study team

No contact information is available for this study as per the public registry record.

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Locations (54)

Hope Research InstitutePhoenix, Arizona, United States
Arizona Research CenterPhoenix, Arizona, United States
Trovare Clinical ResearchBakersfield, California, United States
Velocity Clinical Research - BanningBanning, California, United States
Velocity Clinical Research - San DiegoLa Mesa, California, United States
Probe Clinical ResearchRiverside, California, United States
Pain Management and Injury ReliefThousand Oaks, California, United States
Visionary Investigators NetworkAventura, Florida, United States
Nature Coast Clinical Research - Crystal RiverCrystal River, Florida, United States
JY Research InstituteCutler Bay, Florida, United States
Fleming Island Center for Clinical ResearchFleming Island, Florida, United States
Convenient Medical ResearchHialeah, Florida, United States

+ 42 more locations — full list on the registry record.

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