A Phase 2, Randomized, Double-blind, Placebo-controlled, Parallel-design Study of the Efficacy and Safety of VX-548 in Subjects With Painful Lumbosacral Radiculopathy
Abstract
The purpose of the study is to evaluate the efficacy and safety of VX-548 in treating participants with PLSR.
Conditions: Painful Lumbosacral Radiculopathy.
Primary outcome: Change From Baseline in the Weekly Average of Daily leg Pain Intensity on a Numeric Pain Rating Scale (NPRS).
Enrollment: 218 participants.
How strong is the evidence?
Evidence Hub reads this as a randomized trial, done in people. Its evidence level is 2 of 5 (High · randomized trial). Randomized trials of a reasonable size are the strongest single-study design. Reported size: 218 participants or records.
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