The purpose of the study is to evaluate the efficacy and safety of VX-548 in treating participants with PLSR.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
218
Change From Baseline in the Weekly Average of Daily leg Pain Intensity on a Numeric Pain Rating Scale (NPRS)
Time frame: Baseline, Week 12
Change From Baseline in the Weekly Average of the Daily Sleep Interference Scale (DSIS)
Time frame: Baseline, Week 12
Safety and Tolerability as Assessed by Number of Participants With Adverse Events (AEs) and Serious Adverse Events (SAEs)
Time frame: From Day 1 up to Week 14
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Hope Research Institute
Phoenix, Arizona, United States
Arizona Research Center
Phoenix, Arizona, United States
Trovare Clinical Research
Bakersfield, California, United States
Velocity Clinical Research - Banning
Banning, California, United States
Velocity Clinical Research - San Diego
La Mesa, California, United States
Probe Clinical Research
Riverside, California, United States
Pain Management and Injury Relief
Thousand Oaks, California, United States
Visionary Investigators Network
Aventura, Florida, United States
Nature Coast Clinical Research - Crystal River
Crystal River, Florida, United States
JY Research Institute
Cutler Bay, Florida, United States
...and 44 more locations