A 52-Week, Open-Label, Prospective, Multicenter, International Study of a Transition to the Paliperidone Palmitate 3-Month Formulation In Patients with Schizophrenia Previously Stabilized on the Pa...
This historical record does not confirm current site availability.
Understand this study
What did researchers investigate?
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.
Who was this study for?
This study was for people with schizophrenia. Other eligibility criteria applied.
- Listed locations
- Croatia · Denmark and 6 more locations
- Study phase
- Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
Study information
- Recruitment status
- Completed
- Enrollment listed in the registry
- 300
- Sponsor
- Janssen-Cilag International NV
- Sponsor type
- Unknown or unclear
- Study type
- Drug
- Intervention type
- Medication / drug
- Study phase
- Phase 3Usually a larger study designed to confirm effectiveness and safety in a broader group.
- Locations
- United Kingdom, Croatia, Denmark, ...
- Age range
- Not clearly listed
- Official registry ID
- EUCTR 2015-004835-10
- Official title
Show the full official title
A 52-Week, Open-Label, Prospective, Multicenter, International Study of a Transition to the Paliperidone Palmitate 3-Month Formulation In Patients with Schizophrenia Previously Stabilized on the Pa...
Recruitment & locations
CompletedCroatia · Denmark · Germany
5 more locations
- Greece
- Italy
- Netherlands
- Spain
- United Kingdom
Registry details
- Germany — Completed
- Denmark — Completed
- Spain — Completed
- United Kingdom — Completed
- Greece — Completed
- Croatia — Completed
- Italy — Completed
- Netherlands — Completed
Questions about this study
Who is behind this study?
The study sponsor is Janssen-Cilag International NV.
Who was this study for?
This study was for people with schizophrenia. Other eligibility criteria applied.
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