drugset / Trial / NCT00354094

[S,S]-Reboxetine Long Term Safety Study In Post-Shingles Pain.

NCT00354094 ↗

Phase 2 Terminated 600 enrolled Pfizer
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to assess the long term (up to 2 years) safety and tolerability of \[S,S\]-Reboxetine in patients with pain after shingles.

Timeline

Start
2006-11
Primary completion
—
Completion
2007-10

Outcome

Outcome not reported

Stopped (Business): “The study was stopped due to business/operational issues.”

Drugs

EvaluationDrugModalityDoseRoute
Subject [S,S]-Reboxetine Unknown — —

Indications

No indication recorded.