- Trials with a EudraCT protocol (73)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
73 result(s) found for: Motor neuropathy.
Displaying page 1 of 4.
EudraCT Number: 2008-005748-18 | Sponsor Protocol Number: SN07NE080 | Start Date*: 2009-01-02 | |||||||||||
Sponsor Name:Greater Glasgow and Clyde NHS Board and The University Of Glasgow | |||||||||||||
Full Title: SAFETY AND TOLERABILITY OF ECULIZUMAB IN THE TREATMENT OF MULTIFOCAL MOTOR NEUROPATHY: AN OPEN LABEL STUDY | |||||||||||||
Medical condition: Multifocal motor neuropathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
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: 2009-012073-34 | Sponsor Protocol Number: R0000063 | Start Date*: 2009-07-08 | |||||||||||
Sponsor Name:Radboud University Nijmegen Medical Centre | |||||||||||||
Full Title: Botulinum toxin for treating calf muscle spasticity in Hereditary Spastic Paraparesis (HSP): functional effects on dynamic balance and gait | |||||||||||||
Medical condition: Subjects with hereditary spastic paraparesis (HSP) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-013841-27 | Sponsor Protocol Number: 160604 | Start Date*: 2009-12-17 | |||||||||||
Sponsor Name:Baxter Innovations GmbH | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo Controlled, Cross-over Study of the Effectiveness of Immune Globulin Intravenous (Human), 10% (IGIV, 10%) for the Treatment of Multofocl Motor Neuropathy | |||||||||||||
Medical condition: Multifocal motor neuropathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
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: 2007-000710-37 | Sponsor Protocol Number: ZLB06_006CR | Start Date*: 2007-12-10 | |||||||||||
Sponsor Name:CSL Behring AG | |||||||||||||
Full Title: A multicentre study of subcutaneous immunoglobulin in patients with Multifocal Motor Neuropathy (MMN) | |||||||||||||
Medical condition: Patients with multifocal motor neuropathy, who are treated successful with IVIG and had a stable IVIG treatment schedule for at least 12 weeks prior to screening. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000398-21 | Sponsor Protocol Number: ESTEVE-SIGM-202 | Start Date*: 2012-06-21 | |||||||||||
Sponsor Name:Laboratorios del Dr. Esteve, S.A. | |||||||||||||
Full Title: A proof-of-concept phase 2, randomized, placebo-controlled, double blind, multicentre clinical trial in 2 parallel groups to evaluate the efficacy and safety of E-52862 for reducing the incidence a... | |||||||||||||
Medical condition: OXL-induced chronic neuropathy. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
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 |
EudraCT Number: 2010-022046-25 | Sponsor Protocol Number: Zellweger | Start Date*: Information not available in EudraCT | ||||||||||||||||
Sponsor Name:Department of Pediatric Gastroenterology, Academic Medical Centre | ||||||||||||||||||
Full Title: Cholic acid treatment in Peroxisomal Biogenesis Disorders (Zellweger spectrum): biochemical and clinical effects. | ||||||||||||||||||
Medical condition: Peroxisomal biogenesis disorder Synonym: Zellweger spectrum disorder This syndrome encompasses a spectrum of severity in symptoms Previously the disorder was subdivided into three disorders based... | ||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003054-16 | Sponsor Protocol Number: DDZ-BOND-2017 | Start Date*: 2018-07-27 | |||||||||||
Sponsor Name:Wörwag Pharma GmbH & co. KG | |||||||||||||
Full Title: Randomized double-blind, placebo-controlled parallel group study over 12 months to assess the effects of treatment with benfotiamine on morphometric, neurophysiological, and clinical measures in ty... | |||||||||||||
Medical condition: diabetic polyneuropathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-003302-50 | Sponsor Protocol Number: ARGX-117-2002 | Start Date*: 2022-01-31 | |||||||||||
Sponsor Name:argenx BV | |||||||||||||
Full Title: A Phase 2, Randomized, Double-Blinded, Placebo-Controlled, Parallel-Group, Multicenter Trial to Evaluate the Safety and Tolerability, Efficacy, Pharmacokinetics, Pharmacodynamics, and Immunogenicit... | |||||||||||||
Medical condition: Multifocal Motor Neuropathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) ES (Completed) DE (Completed) BE (Completed) IT (Completed) PL (Completed) AT (Completed) NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-003453-18 | Sponsor Protocol Number: RH-2015-200 | Start Date*: 2015-11-25 | |||||||||||
Sponsor Name:Rigshospitalet | |||||||||||||
Full Title: A Randomized, Single-blinded, Cross-over Study investigating the Non-inferiority of Efficacy and Safety of HyQvia in comparison with Conventional Subcutaneous Ig Therapy in Multifocal Motor Neuropa... | |||||||||||||
Medical condition: Multifocal Motor Neuropathy (MMN) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001246-17 | Sponsor Protocol Number: CBX129801-DN-201 | Start Date*: 2013-05-28 |
Sponsor Name:Cebix Incorporated | ||
Full Title: A Phase 2b, Randomized, Double-Blind, Placebo Controlled Study to Evaluate the Safety and Efficacy of CBX129801 (Ersatta™), Long-Acting Synthetic C-Peptide, in Type 1 Diabetes Mellitus Subjects wit... | ||
Medical condition: Mild to moderate diabetic peripheral neuropathy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-002523-42 | Sponsor Protocol Number: D5680C00002 | Start Date*: 2018-10-22 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled, dose-response study of the efficacy and safety of MEDI7352 in subjects with painful diabetic neuropathy | |||||||||||||
Medical condition: Painful diabetic neuropathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) ES (Prematurely Ended) PL (Prematurely Ended) HU (Prematurely Ended) DK (Completed) RO (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003197-57 | Sponsor Protocol Number: A0081181 | Start Date*: 2012-11-09 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Pfizer Worldwide Research and Development | ||||||||||||||||||||||||||||||||||||||
Full Title: A MULTIPLE DOSE PHARMACOKINETIC OPEN-LABEL STUDY OF PREGABALIN (LYRICA) IN HEALTHY LACTATING WOMEN | ||||||||||||||||||||||||||||||||||||||
Medical condition: neuropathic pain associated with diabetic peripheral neuropathy postherpetic neuralgia neuropathic pain related to spinal cord injury (US), fibromyalgia (US, JP) treatment of central and periphe... | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-006488-22 | Sponsor Protocol Number: E2007-G000-227 | Start Date*: 2007-10-03 | |||||||||||
Sponsor Name:Eisai Limited | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel- Group Trial to Evaluate the Efficacy and Safety of E2007 in Patients with Painful Diabetic Neuropathy | |||||||||||||
Medical condition: Painful Diabetic Neuropathy | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) LT (Completed) DE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000585-30 | Sponsor Protocol Number: I16016 | Start Date*: 2017-12-13 | ||||||||||||||||
Sponsor Name:CHU de Limoges | ||||||||||||||||||
Full Title: Pilot study, single-blind, candesartan versus usual care of peripheral neuropathy development induced by vincristine (PNIV) in patients treated for lymphoma B. | ||||||||||||||||||
Medical condition: peripheral neuropathy | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-001218-26 | Sponsor Protocol Number: TRO19622 CL E Q 1204-1 | Start Date*: 2008-06-19 | |||||||||||
Sponsor Name:TROPHOS SA | |||||||||||||
Full Title: A double blind, placebo controlled study of the effect of 330mg QD of TRO19622 in the treatment of Chemotherapy Induced Peripheral Neuropathy. | |||||||||||||
Medical condition: Symptoms of chemotherapy induced peripheral neuropathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-005326-23 | Sponsor Protocol Number: PHRC-K2020PEZET | Start Date*: 2022-01-24 |
Sponsor Name:CHU de Clermont-Ferrand | ||
Full Title: Evaluation of the efficacy of donepezil in the treatment of oxaliplatin-induced peripheral neuropathy: proof of concept study | ||
Medical condition: Oxaliplatine-induced peripheral neuropathy | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-002810-15 | Sponsor Protocol Number: CHUB-Neuro-ENMG-MS | Start Date*: 2021-06-25 | |||||||||||
Sponsor Name:CHU Brugmann | |||||||||||||
Full Title: Peripheral neuropathy as potential side effect in patients with multiple sclerosis treated with teriflunomide. | |||||||||||||
Medical condition: Multiple sclerosis, treated with teriflunomide | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
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