A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Dose-Response Study to Evaluate Efficacy and Safety of Prolonged Release (PR) OROS® methylphenidate (54 and 72 mg/day) i...
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.
- Listed locations
- Belgium · Denmark and 7 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 N.V., Turnhoutseweg 30, B-2340 Beerse, Belgium
- 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
- France, United Kingdom, Belgium, ...
- Age range
- Not clearly listed
- Official registry ID
- EUCTR 2007-002111-82
- Official title
Show the full official title
A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Dose-Response Study to Evaluate Efficacy and Safety of Prolonged Release (PR) OROS® methylphenidate (54 and 72 mg/day) i...
Recruitment & locations
CompletedBelgium · Denmark · Finland
6 more locations
- France
- Germany
- Netherlands
- Spain
- Sweden
- United Kingdom
Registry details
- Belgium — Completed
- Germany — Completed
- Denmark — Completed
- Spain — Completed
- Finland — Completed
- France — Completed
- United Kingdom — Completed
- Netherlands — Completed
- Sweden — Completed
Questions about this study
Who is behind this study?
The study sponsor is Janssen-Cilag International N.V., Turnhoutseweg 30, B-2340 Beerse, Belgium.
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