A multi-center, open-label, parallel-group, randomized, flexible dose study to evaluate the safety and tolerability of switching from existing atypical antipsychotics to bifeprunox in subjects with...
This historical record does not confirm current site availability.
Understand this study
What is this study about?
This EU register entry describes an interventional medicine trial, designed to assign participants a study treatment. The protocol sets out the treatment, eligibility criteria and assessments. Check the source details below for country statuses and any transfer to CTIS.
- Listed locations
- Czechia · Estonia and 2 more locations
- Study phase
- Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
What to know before participating
This is historical registry information. What is the current study status and protocol?
Things to check before joining
- Recruitment status
- Not recruiting
- Enrollment listed in the registry
- 240
- Sponsor
- Solvay Pharmaceuticals Inc
- Sponsor type
- Other organization
- Study type
- Drug
- Intervention type
- Drug
- Study phase
- Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
- Locations
- Czechia, Estonia, Latvia, ...
- Age range
- Not clearly listed
- Official registry ID
- EUCTR 2006-004972-11
- Official title
Show the full official title
A multi-center, open-label, parallel-group, randomized, flexible dose study to evaluate the safety and tolerability of switching from existing atypical antipsychotics to bifeprunox in subjects with...
Recruitment & locations
Czechia · Estonia · Latvia
1 more locations
- Lithuania
Interested in joining this study?
Questions about this study
Who is behind this study?
The study sponsor is Solvay Pharmaceuticals Inc.
Is this study still recruiting?
The historical registry lists this study as not recruiting.
