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CompletedEUCTR 2010-020951-30

A Phase 4, Open-label, Multicentre, 2-Year Safety Study of Lisdexamfetamine Dimesylate in Children and Adolescents Aged 6-17 Years with Attention-Deficit/Hyperactivity Disorder (ADHD)

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.

Listed locations
Belgium · Germany and 7 more locations
Study phase
Phase 4Usually happens after approval, to monitor real-world use, safety, and longer-term outcomes.

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Study clarity

Study information

Study start dateNot clearly listed
Recruitment status
Completed
Enrollment listed in the registry
300
Sponsor
Shire Pharmaceutical Development Ltd
Sponsor type
Pharmaceutical company
Study type
Drug
Intervention type
Drug
Study phase
Phase 4Usually happens after approval, to monitor real-world use, safety, and longer-term outcomes.
Locations
United Kingdom, Belgium, Germany, ...
Age range
Not clearly listed
Official registry ID
EUCTR 2010-020951-30
Official title
Show the full official title

A Phase 4, Open-label, Multicentre, 2-Year Safety Study of Lisdexamfetamine Dimesylate in Children and Adolescents Aged 6-17 Years with Attention-Deficit/Hyperactivity Disorder (ADHD)

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Recruitment & locations

Completed

Belgium · Germany · Hungary

6 more locations
  • Italy
  • Netherlands
  • Poland
  • Spain
  • Sweden
  • United Kingdom
Registry details
Historical country statuses

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FAQ

Questions about this study

Who is behind this study?

The study sponsor is Shire Pharmaceutical Development Ltd, a pharmaceutical company.

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