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CompletedEUCTR 2007-002111-82

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.

Historical research recordMultiple countriesADHD
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.

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 clarity

Study information

Study start dateNot clearly listed
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...

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Recruitment & locations

Completed

Belgium · Denmark · Finland

6 more locations
  • France
  • Germany
  • Netherlands
  • Spain
  • Sweden
  • United Kingdom
Registry details
Historical country statuses
FAQ

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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