- Trials with a EudraCT protocol (170)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
170 result(s) found for: Brain atrophy.
Displaying page 1 of 9.
EudraCT Number: 2009-014644-11 | Sponsor Protocol Number: MSA-RAS-202 | Start Date*: 2009-12-08 | |||||||||||
Sponsor Name:Teva Pharmaceutical Industries Ltd | |||||||||||||
Full Title: A Multi-centered, Randomized, Double-blind, Placebo-controlled Clinical Trial to Assess the Efficacy, Safety, and Tolerability of Rasagiline Mesylate 1 mg in Patients with Multiple System Atrophy o... | |||||||||||||
Medical condition: Multiple System Atrophy of the Parkinsonian Subtype | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FR (Completed) ES (Completed) HU (Completed) AT (Completed) NL (Completed) IT (Completed) PT (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-003231-29 | Sponsor Protocol Number: ATH434-201 | Start Date*: 2022-07-26 | |||||||||||
Sponsor Name:Alterity Therapeutics Limited | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled Study of ATH434 in Multiple System Atrophy | |||||||||||||
Medical condition: Multiple System Atrophy (MSA) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) FR (Completed) AT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004383-65 | Sponsor Protocol Number: SRK-015-002 | Start Date*: 2019-10-30 | ||||||||||||||||
Sponsor Name:Scholar Rock, Inc. | ||||||||||||||||||
Full Title: Phase 2 Active Treatment Study to Evaluate the Efficacy and Safety of SRK-015 in Patients with Later-Onset Spinal Muscular Atrophy | ||||||||||||||||||
Medical condition: Later Onset Spinal Muscular Atrophy (SMA) | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Completed) ES (Ongoing) DE (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2022-000336-28 | Sponsor Protocol Number: TAK-341-2001 | Start Date*: 2022-10-21 | |||||||||||
Sponsor Name:Takeda Development Center Americas, Inc. | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-Controlled, Phase 2 Study to Evaluate the Efficacy, Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Intravenous TAK-341 in Subjects With Multiple... | |||||||||||||
Medical condition: Multiple System Atrophy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Trial now transitioned) FR (Trial now transitioned) PT (Trial now transitioned) DE (Trial now transitioned) DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-001281-13 | Sponsor Protocol Number: KS-2004-06-SET | Start Date*: 2005-11-15 |
Sponsor Name:DSC Services, s.r.o. | ||
Full Title: Observational Study of Early Interferon beta 1-a Treatment in High Risk Subjects after CIS (SET Study) | ||
Medical condition: Clinically isolated syndrome suspected from demyelinating event (no better explanation for present symptoms) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: CZ (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-018157-23 | Sponsor Protocol Number: D0490C00014 | Start Date*: 2010-11-30 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Phase IIa, Multi-Centre, Double-Blind, Randomised, Placebo-Controlled, Parallel Group 12-Month Treatment, Adaptive Design Study to Assess the Efficacy, Safety, Tolerability, and Pharmacokinetics ... | |||||||||||||
Medical condition: Multiple system atrophy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) ES (Prematurely Ended) AT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002087-12 | Sponsor Protocol Number: BN40703 | Start Date*: 2018-12-07 | ||||||||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | ||||||||||||||||||
Full Title: AN OPEN-LABEL STUDY OF RISDIPLAM IN INFANTS WITH GENETICALLY DIAGNOSED AND PRESYMPTOMATIC SPINAL MUSCULAR ATROPHY | ||||||||||||||||||
Medical condition: Spinal Muscular Atrophy (SMA) | ||||||||||||||||||
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Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Trial now transitioned) PL (Trial now transitioned) IT (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-005024-37 | Sponsor Protocol Number: 202100647 | Start Date*: 2022-01-24 |
Sponsor Name:University Medical Center Groningen | ||
Full Title: Evaluation of [18F]MC225 to measure P-glycoprotein function in neurodegenerative disease | ||
Medical condition: - Alzheimer's disease - Mild Cognitive Impairment - Parkinson's disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2019-001100-38 | Sponsor Protocol Number: BHV3241-301 | Start Date*: 2019-12-13 | |||||||||||
Sponsor Name:Biohaven Pharmaceuticals, Inc | |||||||||||||
Full Title: Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Evaluate the Efficacy and Safety of BHV-3241 in Subjects with Multiple System Atrophy (M-STAR Study) | |||||||||||||
Medical condition: Multiple System Atrophy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) DE (Completed) GB (GB - no longer in EU/EEA) AT (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000506-34 | Sponsor Protocol Number: EMERA006 | Start Date*: 2019-02-04 |
Sponsor Name:NBMI Science Ltd. | ||
Full Title: EMERA006- A pilot, exploratory, randomised, placebo-controlled, double blinded, cross-over, Phase 2a study to explore efficacy and safety of NBMI treatment in patients with Progressive Supranuclear... | ||
Medical condition: PSP or MSA | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: SI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-003622-16 | Sponsor Protocol Number: T214/2016 | Start Date*: 2017-09-19 |
Sponsor Name:Turku University Hospital | ||
Full Title: Targeting SPMS: Effect of teriflunomide treatment on microglial activation in an MS patient cohort at risk of progression. A [11C]PK11195 Brain PET study. | ||
Medical condition: Multiple sclerosis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-002277-22 | Sponsor Protocol Number: AMYPAD-02 | Start Date*: 2018-09-12 |
Sponsor Name:Stichting VUmc | ||
Full Title: AMYPAD Prognostic and Natural History Study (PNHS), an open label, prospective, multicentre, cohort study in individuals without dementia to evaluate the additional value of quantitative amyloid im... | ||
Medical condition: Alzheimer's Disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) ES (Completed) BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-023023-19 | Sponsor Protocol Number: CFTY720DIT01 | Start Date*: 2010-12-28 | |||||||||||
Sponsor Name:NOVARTIS FARMA | |||||||||||||
Full Title: A 18-month, open-label, rater-blinded, randomized, multi-center, active-controlled, parallel-group pilot study to assess efficacy and safety of fingolimod (Gilenya) in comparison to interferon beta... | |||||||||||||
Medical condition: relapsing-remitting multiple sclerosis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002614-10 | Sponsor Protocol Number: 10112 | Start Date*: 2005-05-17 |
Sponsor Name:Lundbeck Limited | ||
Full Title: A 1-Year Randomised, Double-Blind Placebo-Controlled Study to Evaluate the Effects of Memantine on Rate of Brain Atrophy in Patients with Alzheimer’s Disease | ||
Medical condition: Probable Alzheimer's Disease of moderate severity. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-002295-40 | Sponsor Protocol Number: 08-06-2018-paracet | Start Date*: 2018-09-11 |
Sponsor Name:Copenhagen Neuromuscular Center | ||
Full Title: Pharmacokinetics and safety of treatment with paracetamol in children and adults with spinal muscular atrophy and cerebral palsy | ||
Medical condition: Spinal muscular atrophy type II (SMA II) Cerebral palsy (CP) | ||
Disease: | ||
Population Age: Children, Under 18, Adults | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-001836-69 | Sponsor Protocol Number: Vort-MCI_001 | Start Date*: 2021-09-17 |
Sponsor Name:Medical University of Vienna | ||
Full Title: Effects of Vortioxetine in Mild Cognitive Impairment measured by Functional Magnetic Resonance Imaging | ||
Medical condition: Mild cognitive impairment | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-003127-38 | Sponsor Protocol Number: NL71001.029.19 | Start Date*: 2020-04-09 |
Sponsor Name:VUmc Neurology Department | ||
Full Title: Efficacy of add-on high dose simvastatin on markers for disease progression in MS patients treated with ocrelizumab and natalizumab (SIMSON), a phase II clinical trial. | ||
Medical condition: Multiple sclerosis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-005112-42 | Sponsor Protocol Number: C14-62 | Start Date*: 2015-06-22 | |||||||||||
Sponsor Name:INSERM | |||||||||||||
Full Title: A comparative phase2 study assessing the efficacy of triheptanoin, an anaplerotic therapy in Huntington's Disease (TRIHEP 3) | |||||||||||||
Medical condition: Huntington's disease | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005213-22 | Sponsor Protocol Number: SUPREMES-01 | Start Date*: Information not available in EudraCT |
Sponsor Name:Charite Universitätsmedizin Berlin | ||
Full Title: SUPREMES - Sunphenon in progressive forms of multiple sclerosis | ||
Medical condition: primary and secondary progressive forms of multiple sclerosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-024477-39 | Sponsor Protocol Number: 105MS302 | Start Date*: 2011-05-06 | |||||||||||
Sponsor Name:Biogen Idec Limited | |||||||||||||
Full Title: A Dose-Frequency Blinded, Multicenter, Extension Study to Determine the Long-Term Safety and Efficacy of PEGylated Interferon Beta-1a (BIIB017) in Subjects With Relapsing Multiple Sclerosis | |||||||||||||
Medical condition: Relapsing Multiple Sclerosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LV (Completed) BE (Completed) DE (Completed) ES (Completed) BG (Completed) EE (Completed) GB (Completed) GR (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
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