- Trials with a EudraCT protocol (4)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
4 result(s) found for: Social norms.
Displaying page 1 of 1.
| EudraCT Number: 2020-002787-32 | Sponsor Protocol Number: RG_19-172 | Start Date*: 2020-11-16 |
| Sponsor Name:University of Birmingham | ||
| Full Title: Antidepressant for the prevention of DEPression following first episode Psychosis trial | ||
| Medical condition: Patients with First Episode Psychosis. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-005701-32 | Sponsor Protocol Number: B4Z-IT-LYDS | Start Date*: 2006-03-07 | |||||||||||
| Sponsor Name:ELI LILLY | |||||||||||||
| Full Title: An Open-Label Study of the Efficacy of Atomoxetine Hydrochloride on Quality of Life of Children and Adolescents with Attention-Deficit/Hyperactivity Disorder with or without comorbid conditions | |||||||||||||
| Medical condition: Child or adolescent patients with Attention-Deficit/ Hyperactivity Disorder ADHD | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-004700-22 | Sponsor Protocol Number: 1608185 | Start Date*: 2018-02-26 | |||||||||||
| Sponsor Name:CHU SAINT-Etienne | |||||||||||||
| Full Title: Rotation or Change of Biotherapy After TNF blocker treatment failure for axial Spondyloarthritis: The ROC-SpA study | |||||||||||||
| Medical condition: axial Spondyloarthritis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-000304-16 | Sponsor Protocol Number: B4Z-UT-S017 | Start Date*: 2021-12-02 | |||||||||||
| Sponsor Name:Eli Lilly and Company | |||||||||||||
| Full Title: A Randomized, Double-blind Comparison of Atomoxetine Hydrochloride and Placebo for Symptoms of Attention-Deficit/Hyperactivity Disorder in Children and Adolescents With Autism Spectrum Disorder. | |||||||||||||
| Medical condition: Attention-Deficit/Hyperactivity Disorder | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
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