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CompletedNCT01070394

LDX Treatment for ADHD

It tested LDX Treatment for ADHD.

ADHDDrugFrom 18 Years to 55 Years
The study in practice

Understand this study

Who was this study for?

Listed age limits: 18 years to 55 years.

Listed locations
New York, United StatesSee all locations and recruitment

Compensation and expense reimbursement have not been verified for this summary.

Study clarity

Study information

Study start dateFebruary 2010
Recruitment status
Completed
Enrollment listed in the registry
40
Sponsor
NYU Langone Health
Sponsor type
Unknown or unclear
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 4Usually happens after approval, to monitor real-world use, safety, and longer-term outcomes.
Locations
United States
Age range
From 18 Years to 55 Years
Official registry ID
NCT01070394
Official title
Evaluation of Pharmacokinetics and Profile of Clinical Response of Subacute Lisdexamfetamine Dimesylate (Vyvanse) Treatment vs. Clinical Response to Subacute Immediate Release Mixed Amphetamine Salt Therapy in Adult ADHD

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Recruitment & locations

Completed

New York

Checked Official study record (opens in a new tab)
FAQ

Questions about this study

Who is behind this study?

The study sponsor is NYU Langone Health.

Did this study involve medication?

Yes. The study involved medication, including LDX Treatment.

Who was this study for?

Listed age limits: 18 years to 55 years.

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