drugset / Trial / NCT00322764

Phase II Study to Assess RG2417 in the Treatment of Bipolar I Depression

NCT00322764

Phase 2 Completed 80 enrolled Repligen Corporation
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary purpose of this study is to determine the safety and efficacy of oral RG2417 (Uridine) when administered to patients with Bipolar I depression twice daily for six weeks.

Timeline

Start
2006-03
Primary completion
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Uridine Small molecule Oral

Indications