CompletedNCT01322646
Official study titleA Randomized Trial of Interventions for Teenage Drivers With Attention Deficit Hyperactivity Disorder (ADHD)
This study has finished and is no longer accepting participants.
In BuffaloADHDDevice studyAges 16–18
- Countries
- United States
- Sponsor
- State University of New York at Buffalo
CompletedNCT05721235
Official study titleA Multicenter, Dose-Optimized, Open-Label, Safety/Tolerability and Pharmacokinetic Study With Azstarys® in Children 4 and 5 Years of Age With Attention-Deficit/Hyperactivity Disorder
This study has finished and is no longer accepting participants.
Multiple locations, including Little RockADHDMedication studyAges 4–5
- Countries
- United States
- Sponsor
- Corium, Inc.
CompletedNCT02699086
Official study titleA Phase II Tolerability and Efficacy Study of PDC-1421 Treatment in Adult Patients With Attention-Deficit Hyperactivity Disorder (ADHD), Part I
This study has finished and is no longer accepting participants.
In San FranciscoADHDMedication studyAges 18–70
- Countries
- United States
- Sponsor
- BioLite, Inc.
WithdrawnNCT00458445
What is this study about?This study evaluates the safety and effectiveness of SPD465 for people with ADHD.
This study was withdrawn before enrollment.
In TampaADHDMedication studyAges 19–25
- Countries
- United States
- Sponsor
- Shire
CompletedNCT04085172
What is this study about?Researchers compared Guanfacine hydrochloride (TAK-503), Atomoxetine hydrochloride and placebo, tracking side effects to assess safety in children and adolescents with ADHD.
This study has finished and is no longer accepting participants.
Multiple locations, including DothanADHDMedication studyAges 6–17
- Countries
- United States, United Kingdom, Belgium, + 6 others
- Sponsor
- Shire
CompletedNCT01458340
Official study titleA Phase 2 Multicenter, Randomized, Double-Blind, Parallel, Placebo-Controlled Proof-of-Concept Study of TD-9855 in Adults With Attention-Deficit/Hyperactivity Disorder (ADHD)
This study has finished and is no longer accepting participants.
Multiple locations, including BradentonADHDMedication studyAges 18–45
- Countries
- United States
- Sponsor
- Theravance Biopharma
CompletedNCT05137704
Official study titleHealthcare Resources Utilization and Associated Costs of Adult ADHD in England
This study has finished and is no longer accepting participants.
In LondonADHDObservational studyAges 18+
- Countries
- United Kingdom
- Sponsor
- Takeda
CompletedNCT02734693
What is this study about?Researchers compared dasotraline 4mg and placebo to find out how the approaches affected ADHD symptoms in children with ADHD.
This study has finished and is no longer accepting participants.
Multiple locations, including Newport BeachADHDMedication studyAges 6–12
- Countries
- United States
- Sponsor
- Sumitomo Pharma America, Inc.
CompletedNCT03231800
What is this study about?Researchers compared dasotraline and placebo to find out how the approaches affected ADHD symptoms in children with ADHD.
This study has finished and is no longer accepting participants.
Multiple locations, including Newport BeachADHDMedication studyAges 6–12
- Countries
- United States
- Sponsor
- Sumitomo Pharma America, Inc.
CompletedNCT00531752
What is this study about?Researchers compared PF-03654746 and placebo, tracking side effects to assess safety in adults with ADHD.
This study has finished and is no longer accepting participants.
Multiple locations, including LafayetteADHDMedication studyAges 18–55
- Countries
- United States
- Sponsor
- Pfizer
CompletedNCT01624649
Official study titleProspective Follow-Up Observational Study to Examine the Progression of ADHD Drug Treatment and to Analyze Associated Factors
This study has finished and is no longer accepting participants.
Multiple locations, including Bucheon-Si Gyeonggi-DoADHDObservational studyAges 6–15
- Countries
- South Korea
- Sponsor
- Janssen Korea, Ltd., Korea
CompletedNCT00475735
What is this study about?Researchers compared MK0249, Concerta (methylphenidate) and placebo, tracking side effects to assess safety in adults with ADHD.
This study has finished and is no longer accepting participants.
Location not clearly listedADHDMedication studyAges 18–55
- Countries
- Sponsor
- Merck Sharp & Dohme LLC