- Trials with a EudraCT protocol (28)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
28 result(s) found for: Neurological disorders of the eye.
Displaying page 1 of 2.
| EudraCT Number: 2019-005039-94 | Sponsor Protocol Number: IC2019-05 | Start Date*: 2020-12-08 | |||||||||||
| Sponsor Name:Institut Curie | |||||||||||||
| Full Title: RETINO 2018 : Ocular conservative treatment for retinoblastoma: efficacy of the new management strategies and visual outcome. | |||||||||||||
| Medical condition: Retinoblastoma | |||||||||||||
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| Population Age: Newborns, Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-007967-18 | Sponsor Protocol Number: MK0462-088 | Start Date*: 2009-06-25 | |||||||||||
| Sponsor Name:CASA DI CURA PRIVATA S.RAFFAELE - PISANA | |||||||||||||
| Full Title: A Double-Blind, Placebo Crontrolled, Prallel Group Study to Compare the Efficacy of Rizatriptan 10 mg Iyophilized wafer in the Acute Treatment of Migraine in Patients with Unilateral Trigeminal Aut... | |||||||||||||
| Medical condition: not applicable | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-002877-23 | Sponsor Protocol Number: 1.0 | Start Date*: 2019-01-21 | |||||||||||
| Sponsor Name:Abteilung für Neurologie der Medizinischen Universität Innsbruck | |||||||||||||
| Full Title: Oxytocin and social attention in healthy controls and patients with Parkinson's disease. A randomised, double-blind, placebo-controlled, crossover eye tracking study. | |||||||||||||
| Medical condition: Social functioning in Parkinson's disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: AT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-000990-29 | Sponsor Protocol Number: IC2011-02 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:INSTITUT CURIE | |||||||||||||
| Full Title: Multinational européan trial for children with the opsoclonus myoclonus syndrome/dancing eye syndrome. | |||||||||||||
| Medical condition: Opsoclonus myoclonus Syndrome/Dancing Eye Syndrome (OMS/DES) in children with and without neuroblastoma (NBpos and NBneg) | |||||||||||||
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| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) SE (Completed) IT (Prematurely Ended) GB (GB - no longer in EU/EEA) AT (Completed) ES (Ongoing) BE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-000183-29 | Sponsor Protocol Number: REVISION | Start Date*: 2022-03-09 | |||||||||||
| Sponsor Name:Eberhard-Karls University Tübingen, Med. Fac. rep. by University Hospital and its Commercial Director | |||||||||||||
| Full Title: Early Reperfusion Therapy with Intravenous Alteplase for Recovery of VISION in Acute Central Retinal Artery Occlusion (REVISION) - A double-blind randomized placebo-controlled phase III proof-of-co... | |||||||||||||
| Medical condition: Acute non-arteritic central retinal artery occlusion (CRAO) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-001476-11 | Sponsor Protocol Number: AL002-2 | Start Date*: 2020-11-12 | |||||||||||
| Sponsor Name:Alector Inc. | |||||||||||||
| Full Title: A PHASE 2 RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, MULTICENTER STUDY TO EVALUATE THE EFFICACY AND SAFETY OF AL002 IN PARTICIPANTS WITH EARLY ALZHEIMER’S DISEASE | |||||||||||||
| Medical condition: Early Alzheimer’s Disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) PL (Completed) DE (Completed) IT (Completed) FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-020515-37 | Sponsor Protocol Number: CFTY720D2399 | Start Date*: 2010-08-06 | |||||||||||
| Sponsor Name:Novartis Pharma Services AG | |||||||||||||
| Full Title: A single arm, open-label, multicenter study evaluating the long-term, safety and tolerability of 0.5 mg fingolimod (FTY720) administered orally once daily in patients with relapsing forms of multip... | |||||||||||||
| Medical condition: multiple sclerosis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Completed) DE (Completed) PT (Completed) CZ (Completed) ES (Completed) SK (Completed) HU (Completed) GB (Completed) SE (Completed) FR (Completed) EE (Completed) IT (Completed) AT (Completed) GR (Completed) NL (Completed) IE (Completed) BE (Completed) DK (Completed) NO (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-000439-32 | Sponsor Protocol Number: NW-3509/015/II/2019 | Start Date*: 2021-04-28 | |||||||||||
| Sponsor Name:NEWRON PHARMACEUTICALS SPA | |||||||||||||
| Full Title: An open-label, multi-center, extension study to evaluate the long-term safety, tolerability and preliminary efficacy of Evenamide as add-on treatment in patients with treatment-resistant schizophre... | |||||||||||||
| Medical condition: Schizophrenia not responding adequately to current antipsychotic treatment | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-003490-15 | Sponsor Protocol Number: CACZ885D2308 | Start Date*: 2016-04-14 | ||||||||||||||||||||||||||
| Sponsor Name:Novartis Pharmaceuticals | ||||||||||||||||||||||||||||
| Full Title: An Open-label, Efficacy and Safety Study of Canakinumab (Anti-interleukin-1β Monoclonal Antibody) Administered for 6 Months (24 Weeks) in Japanese Patients With the Following Cryopyrin-associated P... | ||||||||||||||||||||||||||||
| Medical condition: Cryopyrin-associated Periodic Syndromes Familial Cold Autoinflammatory Syndrome Muckle-Wells Syndrome Neonatal Onset Multisystem Inflammatory Disease | ||||||||||||||||||||||||||||
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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: 2009-014269-25 | Sponsor Protocol Number: A0081096 | Start Date*: 2009-12-18 | |||||||||||
| Sponsor Name:Pfizer Inc | |||||||||||||
| Full Title: PROSPECTIVE RANDOMIZED 12-WEEK CONTROLLED STUDY OF VISUAL FIELD CHANGE IN SUBJECTS WITH PARTIAL SEIZURES RECEIVING PREGABALIN OR PLACEBO | |||||||||||||
| Medical condition: EPILEPSY WITH PARTIAL SEIZURE | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) CZ (Completed) PL (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-020098-18 | Sponsor Protocol Number: 2010-605 | Start Date*: 2010-09-09 | |||||||||||
| Sponsor Name:HOSPICES CIVILS DE LYON | |||||||||||||
| Full Title: CrYSTobs A cohort of patients with cystinosis : compliance to cysteamine and neurological complications An auxiliary study to Raptor RP103 03 and RP103 04 | |||||||||||||
| Medical condition: nephropatic cystinosis | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-022791-31 | Sponsor Protocol Number: D01092010AZNTG | Start Date*: Information not available in EudraCT | |||||||||||||||||||||||||||||||
| Sponsor Name:University Erlangen-Nuremberg | |||||||||||||||||||||||||||||||||
| Full Title: Contrast sensitivity of patients with normal tension glaucoma by application of Azarga® | |||||||||||||||||||||||||||||||||
| Medical condition: The effect of AZARGA(R) on the central and spacial-temporal contrast sensitivity of patients with normal tension glaucoma will be examined. Healthy controls are required to prove the disease specif... | |||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: DE (Ongoing) | |||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2020-000437-41 | Sponsor Protocol Number: NW-3509/014/II/2019 | Start Date*: 2021-02-24 | |||||||||||
| Sponsor Name:NEWRON PHARMACEUTICALS SPA | |||||||||||||
| Full Title: A pilot, open-label, rater-blinded, randomized, parallel-group, multi-center study to evaluate the safety, tolerability and preliminary efficacy of three add-on fixed doses of Evenamide in patients... | |||||||||||||
| Medical condition: Schizophrenia not responding adequately to current antipsychotic treatment | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-005319-30 | Sponsor Protocol Number: 217917 | Start Date*: 2022-11-02 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:GlaxoSmithKline Biologicals | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: A phase 3b, open-label, multi-country, multi-centre, long-term follow-up study of ZOSTER-049 (follow-up of ZOSTER-006/022 studies) to assess the prophylactic efficacy, safety and persistence of imm... | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Vaccination against HZ and its related complications in adults older than 50 years (at the time of primary vaccination). | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: DE (Trial now transitioned) SE (Trial now transitioned) FR (Trial now transitioned) FI (Trial now transitioned) EE (Trial now transitioned) ES (Ongoing) IT (Trial now transitioned) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2014-000395-26 | Sponsor Protocol Number: GER-BGT-13-10586 | Start Date*: 2015-08-07 | |||||||||||
| Sponsor Name:Biogen GmbH | |||||||||||||
| Full Title: A 3-year open-label, exploratory, single arm study to describe long term changes in the visual system of patients with relapsing remitting multiple sclerosis (RRMS) on oral dimethyl fumarate | |||||||||||||
| Medical condition: Relapsing Remitting Multiple Sclerosis (RRMS) | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-004253-16 | Sponsor Protocol Number: NMSNab2study | Start Date*: 2018-04-13 | |||||||||||
| Sponsor Name:Medizinische Universität Innsbruck, Universitätsklinik für Neurologie | |||||||||||||
| Full Title: Nabilone for non-motor symptoms in Parkinson’s disease: An open-label study to evaluate long-term safety and efficacy | |||||||||||||
| Medical condition: Subject with non-Motor symptoms of Parkinson´s disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: 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: 2020-004000-33 | Sponsor Protocol Number: INZ701-201 | Start Date*: 2021-06-10 | |||||||||||
| Sponsor Name:Inozyme Pharma, Inc. | |||||||||||||
| Full Title: A Phase 1/2, Open-Label, Multiple Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of INZ-701 Followed by an Open-Label Long-Term Extension Period i... | |||||||||||||
| Medical condition: Treatment of patients with ABCC6 Deficiency Manifesting as Pseudoxanthoma elasticum (PXE) | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-005761-23 | Sponsor Protocol Number: CTD-TCNPC-201 | Start Date*: 2016-09-26 | |||||||||||
| Sponsor Name:Cyclo Therapeutics, Inc. | |||||||||||||
| Full Title: A Phase I/II study to evaluate the safety and pharmacokinetics of intravenous Trappsol Cyclo (HP-β-CD) in patients with Niemann-Pick disease type C (NPC-1) and the pharmacodynamic effects of treatm... | |||||||||||||
| Medical condition: Niemann-Pick disease type C | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) SE (Completed) IT (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-003757-28 | Sponsor Protocol Number: MEX-NM-301 | Start Date*: 2020-06-24 | |||||||||||
| Sponsor Name:Lupin Europe GmbH | |||||||||||||
| Full Title: An Open-label, non-Comparative Study to Evaluate the Steady-State Pharmacokinetics, Safety, and Efficacy of Mexiletine in Adolescents and Children with Myotonic Disorders | |||||||||||||
| Medical condition: Myotonic disorders: Nondystrophic myotonias (NDM) or myotonic dystrophies (DM, type 1 or type 2); ICD-10 code G71.1 | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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