drugset / Trial / NCT00353808

A Trial Assessing The Long Term Safety And Tolerability Of [S,S]-Reboxetine In Patients With Post-Shingles Pain.

NCT00353808 ↗

Phase 2 Terminated 112 enrolled Pfizer
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to assess the long-term safety and tolerability of \[S,S\]-Reboxetine in patients with chronic pain following shingles. This is the extension study of Protocol A6061026.

Timeline

Start
2006-07
Primary completion
—
Completion
2007-10

Outcome

Outcome not reported

Stopped: “This study has been terminated early as the esreboxetine development program is being discontinued. There are no safety or efficacy concerns.”

Drugs

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

Indications

No indication recorded.