drugset / Trial / NCT00735267

A 52-Week Open-Label Safety Study of PD 0332334 in Subjects With Generalized Anxiety Disorder (GAD)

NCT00735267

Phase 3 Terminated 468 enrolled Pfizer
Non-randomizedSingle-groupOpen-labelTreatment

Summary

This study will assess the long-term safety and tolerability of 350 to 600 mg/day of PD 0332334 administered in split dose (twice daily) in subjects with Generalized Anxiety Disorder.

Timeline

Start
2008-10
Primary completion
2009-04
Completion
2009-04

Drugs

EvaluationDrugModalityDoseRoute
Subject IMAGABALIN Other / unclassified 350 mg Oral
Subject IMAGABALIN Other / unclassified 600 mg Oral