- Trials with a EudraCT protocol (9)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
9 result(s) found for: Mental Health Policy.
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EudraCT Number: 2006-004647-37 | Sponsor Protocol Number: G0373 | Start Date*: 2006-11-06 | |||||||||||
Sponsor Name:Bangor University | |||||||||||||
Full Title: Folate Augmentation of Treatment – Evaluation of Depression: a randomised controlled trial | |||||||||||||
Medical condition: Individuals with moderate to severe depression according to ICD-10 criteria. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001384-87 | Sponsor Protocol Number: WN29722 | Start Date*: 2020-10-19 | ||||||||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | ||||||||||||||||||
Full Title: A PHASE II, MULTICENTER, OPEN-LABEL, SINGLE-ARM STUDY TO EVALUATE THE PHARMACODYNAMIC EFFECTS OF ONCE WEEKLY ADMINISTRATION OF GANTENERUMAB IN PARTICIPANTS WITH EARLY (PRODOMAL TO MILD) ALZHEIMER'S... | ||||||||||||||||||
Medical condition: Alzheimer's Disease (AD) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Prematurely Ended) BE (Completed) FR (Completed) IT (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-000766-42 | Sponsor Protocol Number: WN42171 | Start Date*: 2020-07-23 | ||||||||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | ||||||||||||||||||
Full Title: AN OPEN-LABEL, MULTICENTER, ROLLOVER STUDY TO EVALUATE THE SAFETY, TOLERABILITY, AND EFFICACY OF LONG-TERM GANTENERUMAB ADMINISTRATION IN PARTICIPANTS WITH ALZHEIMER'S DISEASE | ||||||||||||||||||
Medical condition: Alzheimer's Disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DK (Completed) PT (Prematurely Ended) PL (Prematurely Ended) HU (Completed) DE (Completed) FR (Ongoing) IT (Prematurely Ended) LT (Ongoing) NL (Completed) BE (Completed) FI (Completed) HR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-005387-22 | Sponsor Protocol Number: ACP-103-069 | Start Date*: 2022-06-27 | |||||||||||
Sponsor Name:Acadia Pharmaceuticals Inc. | |||||||||||||
Full Title: A Phase 2, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of Pimavanserin for the Treatment of Irritability Associated With Autism Spectrum Disorder | |||||||||||||
Medical condition: Treatment of irritability associated with autistic disorder in children and adolescents with ASD | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) FR (Ongoing) HU (Ongoing) PL (Ongoing) IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003666-41 | Sponsor Protocol Number: MEC2020-0078 | Start Date*: 2020-04-21 | |||||||||||
Sponsor Name:Erasmus MC University Medical Center | |||||||||||||
Full Title: Doxapram versus placebo in preterm newborns: an international double blinded multicenter randomized controlled trial. | |||||||||||||
Medical condition: Preterm infants are at high risk of respiratory failure due to immaturity of the respiratory system. Respiratory failure is caused by a comprised lung function and impaired control of breathing. Co... | |||||||||||||
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Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) BE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002584-25 | Sponsor Protocol Number: 10/46/01 | Start Date*: 2014-11-06 | |||||||||||
Sponsor Name:King's College London [...] | |||||||||||||
Full Title: Naltrexone Enhanced Addiction Treatment (NEAT): A randomised controlled trial of the clinical and cost-effectiveness of extended-release naltrexone and oral naltrexone. | |||||||||||||
Medical condition: Opiate addiction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000986-37 | Sponsor Protocol Number: F1D-MC-HGKB | Start Date*: 2004-11-26 |
Sponsor Name:Eli Lilly and Company Limited | ||
Full Title: An Open-Label Study of Intramuscular Olanzapine Depot in Patients With Schizophrenia or Schizoaffective Disorder | ||
Medical condition: Schizophrenia or Schizoaffective Disorder | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SK (Completed) CZ (Completed) ES (Completed) SE (Completed) BE (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-002328-18 | Sponsor Protocol Number: BP40657 | Start Date*: 2018-12-19 | ||||||||||||||||
Sponsor Name:F. Hoffman-La Roche Ltd. | ||||||||||||||||||
Full Title: A RANDOMIZED, MULTICENTER, PHASE Ib/III STUDY TO INVESTIGATE THE PHARMACOKINETICS, EFFICACY, AND SAFETY OF ATEZOLIZUMAB SUBCUTANEOUS COMPARED WITH ATEZOLIZUMAB INTRAVENOUS IN PATIENTS WITH PREVIOUS... | ||||||||||||||||||
Medical condition: Non-small cell lung cancer (NSCLC) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: LV (Ongoing) PL (Ongoing) HU (Ongoing) GR (Ongoing) BG (Prematurely Ended) IT (Ongoing) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-002005-19 | Sponsor Protocol Number: TTP488-301 | Start Date*: 2016-08-19 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:vTv THERAPEUTICS LLC | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: RANDOMIZED, DOUBLE-BLIND, PLACEBO CONTROLLED, MULTI-CENTER REGISTRATION TRIAL TO EVALUATE THE EFFICACY AND SAFETY OF TTP488 IN PATIENTS WITH MILD ALZHEIMER'S DISEASE RECEIVING ACETYLCHOLINESTERASE ... | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: MILD ALZHEIMER'S DISEASE RECEIVING ACETYLCHOLINESTERASE INHIBITORS AND/OR MEMANTINE | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) IE (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
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