- Trials with a EudraCT protocol (601)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
601 result(s) found for: Motor system.
Displaying page 1 of 31.
EudraCT Number: 2014-005367-32 | Sponsor Protocol Number: PROMISE | Start Date*: 2016-02-29 | |||||||||||
Sponsor Name:FONDAZIONE IRCCS ISTITUTO NEUROLOGICO CARLO BESTA | |||||||||||||
Full Title: PROTEIN MISFOLDING, AMYOTROPHIC LATERAL SCLEROSIS AND GUANABENZ: A PHASE II RCT WITH FUTILITY DESIGN | |||||||||||||
Medical condition: Amiotrophic Lateral Sclerosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004129-89 | Sponsor Protocol Number: Motor-Neuromod_01, Part I-III | Start Date*: 2005-09-19 |
Sponsor Name:Universitätsklinikum Münster | ||
Full Title: Potentiation of procedural motor learning by pharmacological neuromodulation and brain stimulation | ||
Medical condition: Healthy volunteers Patients in the chronic stage (> 1 year) after stroke | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2014-004501-32 | Sponsor Protocol Number: NL51240.018.14 | Start Date*: 2014-12-11 |
Sponsor Name:Academic Medical Center | ||
Full Title: Infusion VErsus STimulation, a cost-effectiveness analysis of the treatment in advanced Parkinson's disease comparing Continuous Intrajejunal Levodopa Infusion to the traditional standard treetment... | ||
Medical condition: Patients with advanced PD who's motor symptoms — severe response fluctuations, dyskinesias, painful dystonia and / or bradykinesia — cannot be controlled despite optimal oral pharmacological therapy. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2019-002827-14 | Sponsor Protocol Number: TreatSPG11 | Start Date*: 2021-01-19 | |||||||||||
Sponsor Name:IRCCS Fondazione Stella Maris | |||||||||||||
Full Title: Phase 2 pharmacological experimental study to test the safety of miglustat in subjects with hereditary spastic paraplegia type 11 | |||||||||||||
Medical condition: Spastic paraparesis type 11 (SPG11), caused by mutations in spatacsin protein, is characterized by the association of peripheral neuropathy, parkinsonism, ataxia, cognitive impairment, hypotrophy o... | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004297-34 | Sponsor Protocol Number: 236252 | Start Date*: 2018-03-31 | |||||||||||
Sponsor Name:Aston University | |||||||||||||
Full Title: A placebo controlled double blind randomised controlled proof of concept study of zolpidem for the treatment of motor and cognitive deficits in late-stage Parkinson’s | |||||||||||||
Medical condition: Parkinson's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-001315-44 | Sponsor Protocol Number: TAK-935-18-002(OV935) | Start Date*: 2022-05-24 | ||||||||||||||||||||||||||
Sponsor Name:Takeda Development Center America, Inc. | ||||||||||||||||||||||||||||
Full Title: A Multicenter, Open-label, Pilot Study of TAK-935 (OV935) in Patients With 15Q Duplication Syndrome or CDKL5 Deficiency Disorder (ARCADE Study) | ||||||||||||||||||||||||||||
Medical condition: Epileptic Encephalopathies: Dravet Syndrome, Lennox Gastaut Syndrome, CDKL5 Deficiency Disorder, and Chromosome 15 Duplication Syndrome | ||||||||||||||||||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: Outside EU/EEA | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-004998-32 | Sponsor Protocol Number: ARGX-117-2003 | Start Date*: 2022-12-19 | |||||||||||
Sponsor Name:argenx BV | |||||||||||||
Full Title: A Long-Term Extension of the ARGX-117-2002 Trial to Evaluate the Long-term Safety and Tolerabillity, Efficacy, Pharmacodynamics, Pharmacokinetics, and Immunogenicity of ARGX-117 in Adults with Mult... | |||||||||||||
Medical condition: Multifocal Motor Neuropathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) ES (Trial now transitioned) BE (Trial now transitioned) DE (Trial now transitioned) IT (Trial now transitioned) NL (Trial now transitioned) AT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-004175-73 | Sponsor Protocol Number: HP-CD-CL-2002 | Start Date*: 2017-09-27 | |||||||||||
Sponsor Name:Herantis Pharma Plc | |||||||||||||
Full Title: A Phase I-II, Randomised, Double-Blind, Placebo Controlled, Safety and Tolerability Study of Intermittent Bilateral Intraputamenal Cerebral Dopamine Neurotrophic Factor (CDNF) Infusions Administere... | |||||||||||||
Medical condition: Idiopathic Parkinson's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000155-12 | Sponsor Protocol Number: 2018_49 | Start Date*: 2020-05-12 |
Sponsor Name:InBrain Pharma SAS | ||
Full Title: A new concept of continuous dopaminergic stimulation by cerebroventricular administration of A-dopamine (dopamine stored in anaerobia) for severe motor fluctuations in Parkinson’s disease? | ||
Medical condition: Proof of concept study: prospective, monocentric, controlled randomized study according a cross over design with 2 groups: cerebroventricular administration of A-dopamine versus optimized oral trea... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2009-009868-31 | Sponsor Protocol Number: 80-82310-98-09088 | Start Date*: 2009-06-18 |
Sponsor Name:ZonMW | ||
Full Title: Quality of life, gross motor function, and actual everyday physical activity level in children with spastic Cerebral Palsy: (cost)effectiveness of combined treatment with multilevel botulinum-toxin... | ||
Medical condition: Spastic Cerebral Palsy, GMFCS levels I-III | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-000468-83 | Sponsor Protocol Number: 31-10-273 | Start Date*: 2011-12-15 | |||||||||||
Sponsor Name:Otsuka Pharmaceutical Development & Commercialization, Inc. | |||||||||||||
Full Title: A Multicenter, Randomized, Double-blind, Placebo-controlled Study Evaluating the Safety and Efficacy of Fixed-Dose Once-weekly Oral Aripiprazole in Children and Adolescents with Tourette’s Disorder | |||||||||||||
Medical condition: Tourette’s Disorder | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) BG (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000467-27 | Sponsor Protocol Number: 31-10-272 | Start Date*: 2011-11-07 | |||||||||||
Sponsor Name:Otsuka Pharmaceutical Development & Commercialization, Inc. | |||||||||||||
Full Title: A Multicenter, Randomized, Double-blind, Placebo-controlled Study Evaluating the Safety and Efficacy of Flexible-Dose Once-weekly Oral Aripiprazole in Children and Adolescents with Tourette's Disorder | |||||||||||||
Medical condition: Tourette’s Disorder | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000469-11 | Sponsor Protocol Number: 31-10-274 | Start Date*: 2011-12-15 | |||||||||||
Sponsor Name:Otsuka Pharmaceutical Development & Commercialization, Inc. | |||||||||||||
Full Title: An Open-Label, Multicenter Study Evaluating the Safety and Tolerability of Once-weekly Oral Aripiprazole in Children and Adolescents with Tourette’s Disorder | |||||||||||||
Medical condition: Tourette’s Disorder | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) BG (Prematurely Ended) RO (Completed) HU (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-004424-15 | Sponsor Protocol Number: NOE-TTS-211 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Noema Pharma Australia Pty Ltd | |||||||||||||
Full Title: An open-label, Phase IIa, multi-center, 12-week prospective study to evaluate the safety and efficacy of NOE-105 at a daily dose range of 2.5mg to 15mg in adult and adolescent male patients with To... | |||||||||||||
Medical condition: Tourette Syndrome | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003140-83 | Sponsor Protocol Number: NBI-921352-DEE2012 | Start Date*: 2021-10-12 | |||||||||||
Sponsor Name:Neurocrine Biosciences, Inc. | |||||||||||||
Full Title: A Phase 2 Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy, Safety, Tolerability, and Pharmacokinetics of NBI-921352 as Adjunctive Therapy in Subjects with SCN8A Developm... | |||||||||||||
Medical condition: SCN8A Developmental and Epileptic Encephalopathy Syndrome (SCN8A-DEE) | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) DK (Completed) PL (Completed) DE (Completed) BE (Completed) FR (Completed) NL (Completed) ES (Completed) IT (Completed) PT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000100-41 | Sponsor Protocol Number: PN018 | Start Date*: 2018-11-21 | ||||||||||||||||
Sponsor Name:Abide Therapeutics, Inc. | ||||||||||||||||||
Full Title: A Randomized, Placebo-Controlled Study of ABX-1431 in Adult Patients with Tourette Syndrome or Chronic Motor Tic Disorder | ||||||||||||||||||
Medical condition: Tourette syndrome or chronic motor tic disorder | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-003498-41 | Sponsor Protocol Number: D-Fampr | Start Date*: 2015-09-22 |
Sponsor Name:Medical University of Vienna | ||
Full Title: Effects of dalfampridine on mobility in the context of daily life | ||
Medical condition: Motor behaviour and cognition in multiple sclerosis patients | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-004685-10 | Sponsor Protocol Number: PD-1105 | Start Date*: 2019-01-11 | |||||||||||
Sponsor Name:Voyager Therapeutics, Inc. | |||||||||||||
Full Title: A Randomized, Placebo Surgery Controlled, Double-blinded, Multi-center, Phase 2 Clinical Trial, Evaluating the Efficacy and Safety of VY-AADC02 in Advanced Parkinson's Disease With Motor Fluctuatio... | |||||||||||||
Medical condition: Patients with Parkinson's Disease with motor fluctuations. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000755-97 | Sponsor Protocol Number: EPFL-CNBI-2017-01 | Start Date*: 2017-03-16 |
Sponsor Name:Defitech Chair in Brain-Machine Interface, EPFL | ||
Full Title: Brain-computer interface and neuromuscular stimulation for rehabilitation following chronic stroke | ||
Medical condition: I61 - Intracerebral haemorrhage I63 - Cerebral infarction Chronic condition (at least 10 months after occurrence of cerebrovascular accident) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: (No results available) |
EudraCT Number: 2012-001995-12 | Sponsor Protocol Number: I10E-0901 | Start Date*: 2015-05-19 | |||||||||||
Sponsor Name:LFB BIOTECHNOLOGIES | |||||||||||||
Full Title: A European, randomised, double-blind, active comparator-controlled, cross-over, efficacy and safety study of a new 10% ready-to-use liquid human intravenous immunoglobulin (I10E) versus Kiovig® in ... | |||||||||||||
Medical condition: Multifocal motor neuropathy (MMN) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) GB (Completed) ES (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
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