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CompletedNCT00152022

Efficacy and Safety of SPD465 in Adults With Moderately Symptomatic ADHD.

Medication studyAges 18–55
The study in practice

Understand this study

Who was this study for?

Listed age limits: 18 years to 55 years.

Activities
Medication described in the protocol
Compensation
Payment and expense reimbursement have not been verified.
Study clarity

Study information

Study start dateStarted: April 25, 2005
Recruitment status
Completed
Enrollment listed in the registry
412
Sponsor
Shire
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
Not clearly listed
Age range
From 18 Years to 55 Years
Official registry ID
NCT00152022
Official title
Show the full official title

A Phase III, Randomized, Double-blind, Multi-center, Placebo-controlled, Parallel-Group, Safety and Efficacy Study of SPD465 in Adults With Attention-Deficit Hyperactivity Disorder (ADHD).

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Recruitment & locations

Completed

Locations not listed

FAQ

Questions about this study

Who is behind this study?

The study sponsor is Shire.

Who was this study for?

Listed age limits: 18 years to 55 years.

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