drugset / Trial / NCT00064467

Lethargic Depression Study

NCT00064467 ↗

Phase 3 Completed 268 enrolled GlaxoSmithKline
RandomizedParallel-groupDouble-blindTreatment

Summary

This is a study of Major Depressive Disorder (MDD) in patients with decreased energy, pleasure and interests.

Timeline

Start
2003-06
Primary completion
2005-05
Completion
2005-05

Outcome

Met primary endpoint

paper Bupropion XL was superior to placebo at endpoint in reducing the IDS-IVR-30 total score (p = .018) PMID 16848645 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Bupropion Small molecule 300 mg —
Subject Bupropion Small molecule 450 mg —