drugset / Trial / NCT00122837

A Comparison of Duloxetine Hydrochloride, Marketed Comparator, and Placebo in the Treatment of Generalized Anxiety Disorder

NCT00122837 ↗

Phase 3 Completed 560 enrolled Eli Lilly and Company Boehringer Ingelheim · collab
RandomizedParallel-groupDouble-blindTreatment

Summary

This is a clinical trial assessing duloxetine and comparator to placebo in patients who have generalized anxiety disorder.

Timeline

Start
2005-04
Primary completion
—
Completion
2007-01

Outcome

Met primary endpoint

paper Duloxetine 60-120 mg/day met all statistical and clinical criteria for non-inferiority PMID 18635722 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Duloxetine Small molecule 60 mg —
Subject Duloxetine Small molecule 120 mg —
Subject Venlafaxine Small molecule 75 mg —
Subject Venlafaxine Small molecule 225 mg —

Indications