- Trials with a EudraCT protocol (99)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
99 result(s) found for: Ataxia.
Displaying page 2 of 5.
| EudraCT Number: 2010-022315-19 | Sponsor Protocol Number: IEDAT-ERY01-2010 | Start Date*: 2011-01-11 | |||||||||||
| Sponsor Name:ERYDEL S.P.A. | |||||||||||||
| Full Title: Valutazione degli effetti del Desametasone Sodio Fosfato Intra-Eritrocitario sui Sintomi Neurologici in Pazienti con Atassia Teleangectasia | |||||||||||||
| Medical condition: Patients with Ataxia-Teleangectasia (AT) | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-019737-94 | Sponsor Protocol Number: ARPA-IGF1-2010 | Start Date*: 2010-07-13 | |||||||||||
| Sponsor Name:FIBHULP | |||||||||||||
| Full Title: ESTUDIO ABIERTO, DE EFICACIA, TOLERANCIA Y SEGURIDAD DEL TRATAMIENTO CON EL FACTOR TRÓFICO IGF-I EN LA ATAXIA CEREBELOSA DEGENERATIVA | |||||||||||||
| Medical condition: Ataxia cerebelosa degenerativa de grado leve a moderado | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-006156-37 | Sponsor Protocol Number: FA_BBK_8 | Start Date*: 2012-07-10 | |||||||||||
| Sponsor Name:UNIVERSITA' DEGLI STUDI DI NAPOLI FEDERICO II | |||||||||||||
| Full Title: A double-blind, randomized, placebo-controlled, clinical trial to test the efficacy of Epoetin alfa on physical performance of Friedreich Ataxia patients. | |||||||||||||
| Medical condition: FRIEDREICH ATAXIA | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-005312-26 | Sponsor Protocol Number: FACEG | Start Date*: 2013-03-18 | |||||||||||
| Sponsor Name:Hospital of the University of Munich, Grosshadern | |||||||||||||
| Full Title: Sustained release 4-aminopyridine (Fampyra®) in cerebellar gait disorder | |||||||||||||
| Medical condition: cerebellar gait disorder, cerebellar ataxia, sensorimotor adaption and ocular motor disorders, postural sway, dysarthria | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-000338-36 | Sponsor Protocol Number: IEDAT-03-2018 | Start Date*: 2018-05-31 | |||||||||||
| Sponsor Name:EryDel S.p.A. | |||||||||||||
| Full Title: Open-label, Long-term, Extension Treatment using Intra-Erythrocyte Dexamethasone Sodium Phosphate in Patients with Ataxia Telangiectasia Who Participated in the IEDAT-02-2015 Study | |||||||||||||
| Medical condition: Patient with neurological symptoms of Ataxia Telangiectasia | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) DE (Completed) BE (Completed) PL (Completed) GB (GB - no longer in EU/EEA) NO (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-003598-41 | Sponsor Protocol Number: FRDA-GLP1-2014 | Start Date*: 2014-10-02 |
| Sponsor Name:CUB - Hôpital Erasme | ||
| Full Title: Pilot study of incretin analogs as new therapeutics for Friedreich's Ataxia. | ||
| Medical condition: Friedreich's Ataxia | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-005241-31 | Sponsor Protocol Number: IEDAT-02-2015 | Start Date*: 2016-09-14 | |||||||||||
| Sponsor Name:EryDel S.p.A. | |||||||||||||
| Full Title: A Multi-center, Randomized, Double-blind, Placebo-controlled Trial to Evaluate the Effects of Intra-Erythrocyte Dexamethasone Sodium Phosphate on Neurological Symptoms in Patients with Ataxia Telan... | |||||||||||||
| Medical condition: Patient with neurological symptoms of Ataxia Telangiectasia | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) BE (Completed) NO (Completed) ES (Completed) PL (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-002163-17 | Sponsor Protocol Number: 15-138 | Start Date*: 2018-10-25 |
| Sponsor Name:RWTH Aachen University represented by the Center for Translational & Clinical Research Aachen (CTC-A) | ||
| Full Title: A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP, MULTICENTRE STUDY OF THE EFFICACY AND SAFETY OF NICOTINAMIDE IN PATIENTS WITH FRIEDREICHS ATAXIA. | ||
| Medical condition: Friedreich Ataxia | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DE (Prematurely Ended) AT (Prematurely Ended) GB (GB - no longer in EU/EEA) ES (Ongoing) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-016317-20 | Sponsor Protocol Number: SCA_LITIO_12 | Start Date*: 2009-10-26 | |||||||||||
| Sponsor Name:UNIVERSITA` DEGLI STUDI DI NAPOLI FEDERICO II | |||||||||||||
| Full Title: PILOT STUDY TO ASSESS SAFETY AND TOLERABILITY OF LITHIUM ON SPINOCEREBELLAR ATAXIA OF TYPE 2 | |||||||||||||
| Medical condition: Spinocerebellar ataxia type 2 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-001481-23 | Sponsor Protocol Number: P160927J | Start Date*: 2017-09-12 | |||||||||||
| Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
| Full Title: MULTICENTER, RANDOMIZED, DOUBLE BLIND, PLACEBO CONTROLLED CLINICAL TRIAL WITH RILUZOLE IN SPINOCEREBELLAR ATAXIA TYPE 2 | |||||||||||||
| Medical condition: SCA2 patients, both gender, at least 18 years of age | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-000460-34 | Sponsor Protocol Number: ALCAT | Start Date*: 2015-11-18 |
| Sponsor Name:Hospital of the University of Munich | ||
| Full Title: Effects of Acetyl-DL-Leucine on cerebellar ataxia - a multinational, multicenter, randomized, double-blind, placebo-controlled, 2-way crossover phase III trial (ALCAT) | ||
| Medical condition: Cerebellar ataxia is a form of ataxia originating in the cerebellum and is most often caused by neurodegenerative disorders of the cerebellum, either hereditary or sporadic. The leading clinical sy... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2013-000107-17 | Sponsor Protocol Number: EAT2TREAT | Start Date*: 2013-05-22 | |||||||||||
| Sponsor Name:Hospital of the University of Munich, Grosshadern | |||||||||||||
| Full Title: Pharmacological therapy of episodic ataxia type 2: a placebo-controlled comparison of the efficacy of 4-aminopyridine sustained-release (Fampyra TM) and acetazolamide (Acemit TM) | |||||||||||||
| Medical condition: Familial episodic ataxia (EA) represents a genetically and phenotypically diverse group of rare autosomal dominant hereditary disorders characterized by episodes of imbalance and incoordination tha... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-005371-34 | Sponsor Protocol Number: 2 39 00240 133 | Start Date*: 2008-03-18 |
| Sponsor Name:BEAUFOUR IPSEN PHARMA | ||
| Full Title: EFFICACY OF EGb 761® 120 mg bid VERSUS PLACEBO IN PATIENTS SUFFERING FROM FRIEDREICH ATAXIA A 3 months, phase II, randomised, double blind, placebo-controlled, parallel groups, clinical study. | ||
| Medical condition: Out patient suffering from friedreich ataxia aged from 12 to 20 years | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: FR (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2022-003265-38 | Sponsor Protocol Number: PTC743-NEU-005-FA | Start Date*: 2022-10-22 |
| Sponsor Name:PTC Therapeutics, Inc. | ||
| Full Title: An Open-Label Study to Evaluate Pharmacokinetics, Safety, and Efficacy of Vatiquinone in Children With Friedreich Ataxia Younger Than 7 Years of Age | ||
| Medical condition: Friedreich Ataxia | ||
| Disease: | ||
| Population Age: Children, Under 18 | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA | ||
| Trial results: View results | ||
| EudraCT Number: 2005-004122-70 | Sponsor Protocol Number: 04M107 | Start Date*: 2005-11-15 |
| Sponsor Name:Great Ormond Street Hospital | ||
| Full Title: Immunogenicity of conjugate pneumococcal vaccine (Prevenar) in patients with ataxia -telangiectasia (AT) including a randomised study of one versus two doses of vaccine. | ||
| Medical condition: Ataxia Telangiectasia (AT) is a genetic condition in which there is a deficiency of the immune system with excessive susceptibility to pneumonia and other infections. | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2008-000787-16 | Sponsor Protocol Number: C07-22 | Start Date*: 2008-06-12 | |||||||||||
| Sponsor Name:Inserm | |||||||||||||
| Full Title: Etude pilote ouverte de l'effet de la fluoxetine chez des patientes agées de 8 à 28 ans atteintes du Syndrôme de Rett Typique | |||||||||||||
| Medical condition: Sydrome de Rett typique | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
| Trial protocol: FR (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2022-001314-19 | Sponsor Protocol Number: VO659-CT01 | Start Date*: 2023-04-25 | ||||||||||||||||
| Sponsor Name:VICO Therapeutics B.V. | ||||||||||||||||||
| Full Title: A phase 1/2a, open-label trial to investigate the safety, tolerability, pharmacokinetics and pharmacodynamics of multiple ascending doses of intrathecally administered VO659 in participants with sp... | ||||||||||||||||||
| Medical condition: spinocerebellar ataxia types 1, 3 and Huntington’s disease | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Trial now transitioned) NL (Trial now transitioned) IT (Prematurely Ended) DK (Trial now transitioned) ES (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2019-004345-32 | Sponsor Protocol Number: ANAVEX2-73-RS-002 | Start Date*: 2020-05-26 | |||||||||||
| Sponsor Name:Anavex Germany GmbH | |||||||||||||
| Full Title: A Double-Blind, Randomised, Placebo-Controlled, Safety and Efficacy Study of ANAVEX2-73 in Patients with Rett Syndrome | |||||||||||||
| Medical condition: Rett Syndrome | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-004405-64 | Sponsor Protocol Number: MT-2-03 | Start Date*: 2019-03-07 | |||||||||||
| Sponsor Name:Minoryx Therapeutics BE, SA | |||||||||||||
| Full Title: A Double-Blind, Placebo-Controlled Study on the Effects of MIN-102 on Biochemical, Imaging, Neurophysiological, and Clinical Markers in Patients with Friedreich’s Ataxia | |||||||||||||
| Medical condition: Friedreich’s Ataxia | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) FR (Completed) DE (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-003315-63 | Sponsor Protocol Number: ARPA-AMANTADINA-2012 | Start Date*: 2012-10-24 |
| Sponsor Name:FIBHULP | ||
| Full Title: RANDOMIZED, DOUBLE-BLIND, PLACEBO CONTROLLED, STUDY OF EFFECTIVENESS, TOLERABILITY AND SAFETY OF THERAPY WITH AMANTADINE IN DEGENERATIVE ATAXIAS | ||
| Medical condition: Degenerative ataxias | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Completed) | ||
| Trial results: (No results available) | ||
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