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Owensboro, Kentucky 42301


This study will evaluate efficacy and safety of methylphenidate hydrochloride modified release compared to placebo in adult patients with childhood-onset attention deficit/hyperactivity disorder (ADHD).


Inclusion criteria: 1. Diagnosis of attention deficit/hyperactivity disorder (ADHD) which started in childhood 2. Female patients of childbearing potential must be practicing an acceptable method of contraception. Exclusion criteria: 1. Patients with body mass index (BMI) less than 18.5 kg/m2 or more than 35 kg/m2 2. History of alcohol or substance abuse within the last six months. 3. History of seizures or use of anticonvulsant medication. 4. Any psychiatric condition that requires medication or may interfere with study participation. 5. Pre-existing cardiovascular disorders including severe hypertension, heart failure, myocardial infraction, etc. 6. Significant respiratory, hepatic, gastrointestinal, renal, hematological or oncologic disorder 7. Diagnosis of glaucoma, hyperthyroidism, pheochromocytoma 8. Diagnosis or family history of Tourette's syndrome 9. Pre-existing cerebrovascular disorders such as cerebral aneurysm, vascular abnormalities including vasculitis or stroke Other protocol-defined inclusion/exclusion criteria may apply



Primary Contact:

Study Director
Novartis Pharmaceuticals
Novartis Pharmaceuticals

Backup Contact:


Location Contact:

Owensboro, Kentucky 42301
United States

There is no listed contact information for this specific location.

Site Status: N/A

Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

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