Clinical trial

PK Effects of Bifeprunox & Valproate in Bipolar I

NCT00141505 · Solvay Pharmaceuticals, Industry · Completed

Key facts

NCT number NCT00141505
Title PK Effects of Bifeprunox & Valproate in Bipolar I
Official title Placebo-controlled Study on the Pharmacokinetics,Pharmacodynamics, Safety and Tolerability of Concurrent Valproate and Bifeprunox Administration in Subjects With Bipolar I Disorder
Lead sponsor Solvay Pharmaceuticals, Industry
Collaborators H. Lundbeck A/S Industry Wyeth is now a wholly owned subsidiary of Pfizer
Status Completed
Phase Phase 2
Study type Interventional
Conditions Bipolar I Disorder
Intervention type Drug
Interventions Bifeprunox
Start date Feb 1, 2005
Primary completion Dec 1, 2006
Completion Dec 1, 2006
First posted Sep 1, 2005
Last update posted Jan 16, 2015
Countries United States

At a glance

  • 1–9 Study sites
  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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