- Trials with a EudraCT protocol (10)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
10 result(s) found for: dystonia.
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EudraCT Number: 2008-005632-32 | Sponsor Protocol Number: 2008TOXINA | Start Date*: 2009-08-18 | |||||||||||
Sponsor Name:Fundació privada de l'Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau | |||||||||||||
Full Title: INYECCIÓN FRECUENTE DE TOXINA BOTULÍNICA SIN PROTEÍNAS COMPLEJANTES: EVALUACIÓN DEL EFECTO SOBRE EL DOLOR EN DISTONÍA CERVICAL | |||||||||||||
Medical condition: Distonía Cervical | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-002042-19 | Sponsor Protocol Number: FER-LEV-2005-02 | Start Date*: 2005-10-14 |
Sponsor Name:Hospital Sant Joan de Déu | ||
Full Title: Double-blind, placebo controlled cross-over study to assess the efficacy of Levetiracetam in paediatric and childhood non-epileptic myoclonus Estudio cruzado, aleatorizado, doble ciego controlado c... | ||
Medical condition: Non-epileptic myoclonus | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-004360-22 | Sponsor Protocol Number: Huntiam | Start Date*: 2021-10-22 | |||||||||||
Sponsor Name:Centro de Investigación Biomédica en Red de Enfermedades Neurodegenerativas (Ciberned) | |||||||||||||
Full Title: MULTI-TECHNICAL TEST ON THE USE OF COMBINED THERAPY OF THEMIN AND BIOTINE IN PATIENTS WITH HUNTINGTON'S DISEASE | |||||||||||||
Medical condition: Huntington´s disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002662-12 | Sponsor Protocol Number: PSY102 | Start Date*: 2012-12-12 | |||||||||||
Sponsor Name:Psyadon Pharmaceuticals Inc. | |||||||||||||
Full Title: An Outpatient Phase 3 Efficacy Study of Ecopipam (PSYRX 101) in the Symptomatic Treatment of Self-Injurious Behavior in Subjects with Lesch-Nyhan Disease (LND). | |||||||||||||
Medical condition: Self-injurious behavior in subjects with Lesch-Nyhan Disease (LND). | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-003453-28 | Sponsor Protocol Number: SOMCT03 | Start Date*: 2022-03-28 | |||||||||||
Sponsor Name:SOM Innovation Biotech SA (SOM Biotech) | |||||||||||||
Full Title: Phase IIb, randomized, double-blind, placebo-controlled study in parallel groups assessing the efficacy and safety of two doses of SOM3355 in patients suffering from Huntington’s Disease with chore... | |||||||||||||
Medical condition: Huntington’s Disease with choreic movements. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) FR (Completed) IT (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003136-25 | Sponsor Protocol Number: CTD-TCNPC-301 | Start Date*: 2021-10-25 | |||||||||||
Sponsor Name:Cyclo Therapeutics, Inc. | |||||||||||||
Full Title: A Phase 3, Double blind, Randomized, Placebo controlled, Parallel group, Multicenter Study to Evaluate the Safety, Tolerability, and Efficacy of 2000 mg/kg of Trappsol® Cyclo™ (Hydroxypropyl β cycl... | |||||||||||||
Medical condition: Niemann Pick Disease Type C1 | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) DE (Trial now transitioned) PL (Trial now transitioned) IT (Trial now transitioned) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001807-19 | Sponsor Protocol Number: TV50717-CNS-30081 | Start Date*: 2019-11-12 | |||||||||||
Sponsor Name:Teva Branded Pharmaceutical Products R&D, Inc. | |||||||||||||
Full Title: An Open-Label, Long-Term Safety, Tolerability, and Efficacy Study of TEV-50717 (Deutetrabenazine) for the Treatment of Dyskinesia in Cerebral Palsy in Children and Adolescents (Open RECLAIM-DCP) | |||||||||||||
Medical condition: Dyskinesia in cerebral palsy (DCP) | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) PL (Prematurely Ended) DK (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-002088-98 | Sponsor Protocol Number: AN01.01.0012 | Start Date*: 2005-11-07 | |||||||||||
Sponsor Name:Amarin Neuroscience Ltd | |||||||||||||
Full Title: Full title of the trial : A multicentre, multi-national, double-blind, randomised, parallel group placebo-controlled trial of ethyl-EPA (ethyl-icosapent) in patients with Huntington’s Disease | |||||||||||||
Medical condition: HUNTINGTON’S DISEASE | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) ES (Ongoing) AT (Prematurely Ended) IT (Prematurely Ended) PT (Prematurely Ended) DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002187-40 | Sponsor Protocol Number: GS-LHON-CLIN-05 | Start Date*: 2018-03-15 |
Sponsor Name:GENSIGHT BIOLOGICS | ||
Full Title: Efficacy and Safety of Bilateral Intravitreal Injection of GS010: A Randomized, Double-Masked, Placebo-Controlled Trial in Subjects Affected with G11778A ND4 Leber Hereditary Optic Neuropathy for U... | ||
Medical condition: Leber Hereditary Optic Neuropathy due to mutations in the mitochondrial NADH Dehydrogenase 4 gene | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) FR (Completed) GB (GB - no longer in EU/EEA) ES (Ongoing) NL (Ongoing) IT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-004438-93 | Sponsor Protocol Number: CT-ORZY-NPC-002 | Start Date*: 2016-05-09 | |||||||||||
Sponsor Name:Orphazyme A/S | |||||||||||||
Full Title: Arimoclomol prospective double blind, randomised, placebo-controlled study in patients diagnosed with Niemann Pick disease type C | |||||||||||||
Medical condition: Niemann Pick disease type C | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) DE (Completed) IT (Completed) PL (Completed) ES (Ongoing) GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
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