Clinical trial
Twice Daily Titration Study of Bifeprunox in Subjects With Schizophrenia
NCT00139906 · Solvay Pharmaceuticals, Industry · Completed
Key facts
| NCT number | NCT00139906 |
|---|---|
| Title | Twice Daily Titration Study of Bifeprunox in Subjects With Schizophrenia |
| Official title | A Randomized, Double-Blind, Placebo-Controlled, Twice Daily Titration Study of the Safety and Tolerability of Bifeprunox in Subjects With Schizophrenia |
| 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 | Schizophrenia, Schizoaffective Disorder |
| Intervention type | Drug |
| Interventions | Bifeprunox |
| Start date | Aug 1, 2005 |
| Primary completion | Oct 1, 2006 |
| Completion | Oct 1, 2006 |
| First posted | Aug 31, 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: