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CompletedEUCTR 2015-004835-10

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.

Historical research recordMultiple countries
The study in practice

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 clarity

Study information

Study start dateNot clearly listed
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...

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Recruitment & locations

Completed

Croatia · Denmark · Germany

5 more locations
  • Greece
  • Italy
  • Netherlands
  • Spain
  • United Kingdom
Registry details
Historical country statuses
FAQ

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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