CompletedNCT03006367
Official study titleAn Open-label, Single Ascending Dose, Pharmacokinetic and Tolerability Study of NFC-1 in Children and Adolescents (Ages 6-17 Years) With Attention Deficit Hyperactivity Disorder
This study has finished and is no longer accepting participants.
Multiple locations, including MaitlandADHDMedication studyAges 6–17
- Countries
- United States
- Sponsor
- Aevi Genomic Medicine, LLC, a Cerecor company
CompletedNCT00626236
What is this study about?Researchers studied SPN-810, tracking side effects to assess safety and tolerability in children with ADHD.
This study has finished and is no longer accepting participants.
Multiple locations, including BradentonADHDMedication studyAges 6–12
- Countries
- United States
- Sponsor
- Supernus Pharmaceuticals, Inc. (Pharmaceutical company)
CompletedNCT00202605
Official study titleA Phase II, Randomized, Double-Blind, Multi-center, Placebo-controlled, Crossover Study of SPD465 in Adults With Attention-Deficit Hyperactivity Disorder (ADHD)
This study has finished and is no longer accepting participants.
Multiple locations, including Little RockADHDMedication studyAges 18–55
- Countries
- United States
- Sponsor
- Shire
CompletedNCT00150618
Official study titleA Phase III, Randomized, Double-Blind, Multi-Center, Parallel-Group, Placebo-Controlled Safety and Efficacy Study of SPD503 in Children and Adolescents Aged 6-17 With Attention Deficit Hyperactivity Disorder (ADHD)
This study has finished and is no longer accepting participants.
Location not clearly listedADHDMedication studyAges 6–17
- Countries
- Sponsor
- Shire
CompletedNCT00152009
What is this study about?Researchers compared SPD503 (Guanfacine hydrochloride) (2 mg), SPD503 (3 mg), SPD503 (4 mg) and placebo to find out how the approaches affected ADHD symptoms in children and adolescents with ADHD.
This study has finished and is no longer accepting participants.
Location not clearly listedADHDMedication studyAges 6–17
- Countries
- Sponsor
- Shire
CompletedNCT02547428
What is this study about?This study evaluated the safety and effectiveness of CTN SR for people with ADHD.
This study has finished and is no longer accepting participants.
Multiple locations, including Newport BeachADHDMedication studyAges 18–60
- Countries
- United States
- Sponsor
- Otsuka Pharmaceutical Development & Commercialization, Inc. (Pharmaceutical company)
CompletedNCT00151957
Official study titleA Phase III, Multi-center, Open-label Study of Methylphenidate Transdermal System (MTS) in Pediatric Patients Aged 6-12 With Attention-Deficit/Hyperactivity Disorder (ADHD)
This study has finished and is no longer accepting participants.
Location not clearly listedADHDMedication studyAges 6–12
- Countries
- Sponsor
- Noven Therapeutics
CompletedNCT00151996
Official study titleA Phase II, Open-Label Co-Administration Study of SPD503 and Psychostimulants in Children and Adolescents Aged 6-17 With Attention-Deficit/Hyperactivity Disorder (ADHD)
This study has finished and is no longer accepting participants.
Location not clearly listedADHDMedication studyAges 6–17
- Countries
- Sponsor
- Shire
CompletedNCT00152035
Official study titleA Phase III, Multi-center, 12-month, Open-label Safety Study of SPD465 in Adults With Attention-Deficit Hyperactivity Disorder (ADHD).
This study has finished and is no longer accepting participants.
Location not clearly listedADHDMedication studyAges 18–55
- Countries
- Sponsor
- Shire
CompletedNCT00150592
What is this study about?Researchers compared SPD503 (Guanfacine HCl) and placebo, tracking side effects to assess safety and tolerability in children and adolescents with ADHD.
This study has finished and is no longer accepting participants.
Location not clearly listedADHDMedication studyAges 6–17
- Countries
- Sponsor
- Shire
CompletedNCT02674633
Official study titleA Randomized, Controlled, Parallel-group, Intervention Study to Assess At-home, Game-based Digital Therapy for Treating Pediatric Participants Ages 8 to 12 Years Old With Attention Deficit Hyperactivity Disorder (ADHD)
This study has finished and is no longer accepting participants.
Multiple locations, including DothanADHDDevice studyAges 8–12
- Countries
- United States
- Sponsor
- Akili Interactive Labs, Inc.
CompletedNCT02828644
Official study titleAn Exploratory Study to Assess the Sustained Effects of Digital Therapy in Pediatric Subjects 8 to 12 Years Old With Attention Deficit Hyperactivity Disorder (ADHD)
This study has finished and is no longer accepting participants.
Multiple locations, including ScottsdaleADHDDevice studyAges 8–12
- Countries
- United States
- Sponsor
- Akili Interactive Labs, Inc.