- Trials with a EudraCT protocol (443)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (6)
443 result(s) found for: parkinson.
Displaying page 1 of 23.
EudraCT Number: 2007-000801-30 | Sponsor Protocol Number: E2007-G000-318 | Start Date*: 2007-08-01 | |||||||||||
Sponsor Name:Eisai Limited | |||||||||||||
Full Title: A Multi-centre, Open Label Extension Study to Evaluate the Long-term Safety, Tolerability, and Efficacy of E2007 as an Adjunctive Therapy in Levodopa Treated Parkinson's Disease Subjects with Motor... | |||||||||||||
Medical condition: Parkinson's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) LV (Prematurely Ended) LT (Prematurely Ended) EE (Prematurely Ended) PL (Completed) FR (Completed) ES (Completed) IT (Completed) HU (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002339-26 | Sponsor Protocol Number: E2007-G000-303 | Start Date*: 2006-10-05 | |||||||||||
Sponsor Name:Eisai Limited | |||||||||||||
Full Title: A Multi-centre, Open Label Extension Study to Evaluate the Long-term Safety, Tolerability and Efficacy of E2007 as an Adjunctive Therapy in Levodopa Treated Parkinson's Disease Patients with Motor ... | |||||||||||||
Medical condition: Levodopa treated Parkinson's disease patients with motor fluctuations. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) EE (Completed) CZ (Completed) HU (Completed) BE (Completed) SE (Prematurely Ended) GB (Prematurely Ended) AT (Prematurely Ended) DE (Completed) ES (Completed) PT (Prematurely Ended) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-017182-38 | Sponsor Protocol Number: IPX066-B09-03 | Start Date*: 2010-05-14 | |||||||||||
Sponsor Name:Impax Laboratories, Inc. acting through its Impax Pharmaceutical Division (Impax) | |||||||||||||
Full Title: An Open-Label Extension Study of the Safety and Clinical Utility of IPX066 in Subjects with Parkinson´s Disease | |||||||||||||
Medical condition: Idiopathic Parkinson´s disease (paralysis agitans) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: EE (Completed) LV (Completed) LT (Completed) DE (Completed) PL (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011541-24 | Sponsor Protocol Number: TVP-1012/501 | Start Date*: 2009-10-09 | |||||||||||
Sponsor Name:Teva Pharmaceutical Industries Ltd | |||||||||||||
Full Title: An Open-Label, Multi-Center, Follow-Up Study Designed to Evaluate the Long-Term Effects of Rasagiline in Parkinson's Disease Subjects who Participated in the ADAGIO Study | |||||||||||||
Medical condition: Parkinson's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) NL (Completed) HU (Completed) FR (Completed) ES (Completed) IT (Completed) DE (Completed) PT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000148-40 | Sponsor Protocol Number: PDSTAT2015 | Start Date*: 2015-11-09 | ||||||||||||||||
Sponsor Name:Plymouth Hospitals NHS Trust | ||||||||||||||||||
Full Title: Simvastatin as a neuroprotective treatment for Parkinson's disease: a double-blind, randomised, placebo controlled futility study in patients of moderate severity. | ||||||||||||||||||
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: 2004-005234-39 | Sponsor Protocol Number: 2939111 | Start Date*: 2005-05-27 | |||||||||||
Sponsor Name:Orion Corporation, ORION PHARMA, Finland | |||||||||||||
Full Title: Multicentre, randomised, double-blind study to compare Stalevo® to levodopa/carbidopa in patients with Parkinson's disease experiencing symptoms of early wearing-off | |||||||||||||
Medical condition: Parkinson's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) SE (Completed) DK (Completed) FI (Completed) IE (Completed) DE (Completed) LT (Completed) LV (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002697-37 | Sponsor Protocol Number: 14/0382 | Start Date*: 2015-04-15 | ||||||||||||||||
Sponsor Name:University College London | ||||||||||||||||||
Full Title: Single-centre open label exploratory phase IIb pilot study of exogenous oral Melatonin for the treatment of Nocturia in adults with Parkinson’s disease | ||||||||||||||||||
Medical condition: Parkinson's Disease Nocturia | ||||||||||||||||||
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Population Age: | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-000833-12 | Sponsor Protocol Number: NW-1015/015/III/2003 | Start Date*: 2004-12-02 | |||||||||||
Sponsor Name:Newron Pharmaceuticals S.p.A. | |||||||||||||
Full Title: A phase III, double-blind, placebo-controlled study to determine the efficacy and safety of a low (50-100 mg/day) and high (150-200 mg/day) dose range of safinamide, as add-on therapy, in patients ... | |||||||||||||
Medical condition: Early idiopathic Parkinson’s disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000835-27 | Sponsor Protocol Number: NW-1015/017/III/2003 | Start Date*: 2004-12-03 | |||||||||||
Sponsor Name:NEWRON PHARMACEUTICALS | |||||||||||||
Full Title: A phase III, double-blind, placebo-controlled, 12-month extension study to investigate the efficacy and safety of a dose range of safinamide of 50-200 mg/day, as add-on therapy in patients with ear... | |||||||||||||
Medical condition: Parkinson's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-008210-38 | Sponsor Protocol Number: 2008_02/0841 | Start Date*: 2009-04-16 | ||||||||||||||||
Sponsor Name:Chru de Lille | ||||||||||||||||||
Full Title: Effet d’un traitement anti-glutamatergique sur les troubles de la marche avec freezing et sur l’attention dans la maladie de Parkinson: “freezing of gait and glutamate: FOGG-I” | ||||||||||||||||||
Medical condition: Patients ayant une maladie de Parkinson Patients à un stade évolué de la maladie avec des troubles de la marche sévères | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-001722-25 | Sponsor Protocol Number: ZonMw80-83600-98-10226 | Start Date*: 2013-08-27 | |||||||||||
Sponsor Name:VU University Medical Center | |||||||||||||
Full Title: Cholinesterase inhibitors to slow progression of visual hallucinations in Parkinson’s disease: a multi-center placebo-controlled trial (CHEVAL) | |||||||||||||
Medical condition: Parkinson's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000405-23 | Sponsor Protocol Number: Versio_1 | Start Date*: 2018-03-27 | |||||||||||
Sponsor Name:Juha Rinne / PET Centre | |||||||||||||
Full Title: In vivo PET imaging of neuroinflammation in Parkinson’s disease using the purinergic P2X7 receptor ligand [11C]SMW139 (PRI-PD) | |||||||||||||
Medical condition: Parkinson´s disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004006-18 | Sponsor Protocol Number: ParkinsonDPI-3 | Start Date*: 2018-06-07 | |||||||||||
Sponsor Name:Pharmaceutical Technology and Biopharmacy, University of Groningen | |||||||||||||
Full Title: Therapeutic effects of an inhaled levodopa dry powder formulation on the recovery from off periods in patients with Parkinson's disease | |||||||||||||
Medical condition: Parkinson's disease is a progressive neurodegenerative disorder characterized by a lack of dopamine production due to the loss of dopamine producing cells in the substantia nigra. This lack of dopa... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-005422-35 | Sponsor Protocol Number: | Start Date*: 2015-05-28 | |||||||||||
Sponsor Name:Imperial College London-Imperial College Healthcare NHS Trust | |||||||||||||
Full Title: THE ROLE OF BUSPIRONE IN ATTENUATING LEVODOPA-INDUCED DYSKINESIAS IN PATIENTS WITH PARKINSON'S DISEASE: A CLINICAL AND POSITRON EMISSION TOMOGRAPHY STUDY WITH 11C-PHNO. | |||||||||||||
Medical condition: Levodopa induced dyskinesias within Parkinson's disease. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000102-11 | Sponsor Protocol Number: NL55949 | Start Date*: 2016-11-23 | |||||||||||
Sponsor Name:University Medical Center Groningen | |||||||||||||
Full Title: Randomized, double-blind, placebo-controlled trial to evaluate the efficacy of continuous subcutaneous apomorphine infusion in Parkinson’s disease patients with refractory visual hallucinations. | |||||||||||||
Medical condition: Parkinson's disease patients with refractory visual hallucinations | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-000867-65 | Sponsor Protocol Number: C_30990_P1_06 | Start Date*: 2021-04-19 | |||||||||||
Sponsor Name:Luye Pharma Switzerland AG | |||||||||||||
Full Title: Comparative, randomized, open, crossover clinical trial to investigate adhesiveness of a newly developed rotigotine-containing transdermal patch in patients with Parkinson's disease | |||||||||||||
Medical condition: Idiopathic Parkinson's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-023756-82 | Sponsor Protocol Number: TUD-RaSPar-051 | Start Date*: 2011-07-13 | |||||||||||
Sponsor Name:Dresden University of Technology | |||||||||||||
Full Title: Rasagiline treatment for Sleep disorders in Parkinson´s disease | |||||||||||||
Medical condition: sleep disturbances/sleep disorders in patients with Parkinson´s disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002239-41 | Sponsor Protocol Number: SC17.01 | Start Date*: 2018-02-16 | |||||||||||
Sponsor Name:I.R.C.C.S. FONDAZIONE S.LUCIA | |||||||||||||
Full Title: Effects of Safinamide therapy on reuroplasticity in patients with Parkinson's disease | |||||||||||||
Medical condition: Parkinson's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004112-21 | Sponsor Protocol Number: VorDE-PD | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:IRCCS SAN RAFFAELE PISANA GESTITO DA SAN RAFFAELE ROMA SRL | |||||||||||||
Full Title: TOLERABILITY, SAFETY AND EFFICACY OF VORTIOXETINE FOR TREATMENT OF DEPRESSION IN PARKINSON’S DISEASE: A 16 WEEK OPEN LABEL STUDY | |||||||||||||
Medical condition: Depression in Parkinson's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-000361-35 | Sponsor Protocol Number: E2007-E044-205 | Start Date*: 2004-10-18 |
Sponsor Name:Eisai Limited | ||
Full Title: A 48-MONTH OPEN LABEL MULTI-CENTERED EXTENSION STUDY TO EVALUATE THE LONG-TERM SAFETY, TOLERABILITY AND EFFICACY OF E2007 IN PATIENTS WITH PARKINSON’S DISEASE WITH “WEARING OFF” MOTOR FLUCTUATIONS ... | ||
Medical condition: Parkinson's Disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Prematurely Ended) IT (Prematurely Ended) | ||
Trial results: View results |
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