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CompletedNCT00390845

P38 Mitogen-activated Protein (Map) Kinase Inhibitor (SB-681323)Study In Patients With Neuropathic Pain

A Double-blind Placebo-controlled Study of the Efficacy and Safety of the P38 Map Kinase Inhibitor SB681323 in Patients With Neuropathic Pain Following Nerve Trauma

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
50 (actual)
Sponsor
GlaxoSmithKline · Industry
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

This will be a double-blind, placebo controlled cross-over study. After enrolment and initial assessments, subjects will receive oral SB681323 or matching placebo for 14 days. SB681323 will be administered twice daily at a total daily dose of 7.5mg. Sufficient numbers of patients will be recruited to obtain 40 evaluable patients

Conditions

Interventions

TypeNameDescription
DRUGSB68132315 milligrams (mg)/day
DRUGPlacebo

Timeline

Start date
2006-08-30
Primary completion
2008-08-11
Completion
2008-08-11
First posted
2006-10-20
Last updated
2017-08-22

Locations

13 sites across 4 countries: Australia, Germany, Russia, United Kingdom

Source: ClinicalTrials.gov record NCT00390845. Inclusion in this directory is not an endorsement.

P38 Mitogen-activated Protein (Map) Kinase Inhibitor (SB-681323)Study In Patients With Neuropathic Pain (NCT00390845) · Clinical Trials Directory