CompletedPhase 2NCT01748695
A Safety, Tolerability and Efficacy Study of V158866 in Central Neuropathic Pain Following Spinal Cord Injury
Studying Spinal cord injury
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Brigham and Women's Hospital
- Principal Investigator
- Christine N Sang, MD, MPH, MD, MPH, FASABrigham and Women's Hospital
- Intervention
- V158866(drug)
- Enrollment
- 25 target
- Eligibility
- 18-65 years · All sexes
- Timeline
- 2013 – 2015
Study locations (1)
- Translational Pain Research, Brigham and Women's Hospital, Boston, Massachusetts, United States
Collaborators
Vernalis (R&D) Ltd
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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