- Trials with a EudraCT protocol (25)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
25 result(s) found for: Selegiline.
Displaying page 1 of 2.
EudraCT Number: 2006-001261-42 | Sponsor Protocol Number: 3002 | Start Date*: 2006-05-18 |
Sponsor Name:Evotec NeuroSciences GmbH | ||
Full Title: Assessment of Inhibition of Brain MAO-B by EVT 301 after Repeated Dosing to Steady-state in Patients with Alzheimer’s Disease and in Elderly Control Subjects | ||
Medical condition: Subjects with probable Alzheimer's Disease and healthy voulunteers | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-000335-17 | Sponsor Protocol Number: MPR001 | Start Date*: 2014-10-28 |
Sponsor Name:Research and Development University Hospital of North Staffordshire [...] | ||
Full Title: The Effect of Rotigotine on Memory in Idiopathic Parkinson's Disease without Cognitive Impairment | ||
Medical condition: Idiopathic Parkinson's Disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2004-002650-59 | Sponsor Protocol Number: SP824 | Start Date*: 2005-02-03 |
Sponsor Name:SCHWARZ BIOSCIENCES | ||
Full Title: A phase 3b, open-label, multicentre, multinational trial to assess the tolerability of switching subjects from ropinerole, pramipexole or cabergoline to the rotigotine transdermal system and its ef... | ||
Medical condition: Idiopathic Parkinson's disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-002598-21 | Sponsor Protocol Number: SP826 | Start Date*: 2004-12-22 |
Sponsor Name:Schwarz Biosciences GmbH | ||
Full Title: A phase 3b, open-label, multicenter, multinational trial to evaluate the effects of rotigotine transdermal patch on early morning motor impairment and sleep disorders in patients with idiopathic Pa... | ||
Medical condition: Parkinson's Disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-002500-91 | Sponsor Protocol Number: RPC01-3001 | Start Date*: 2015-10-12 | |||||||||||
Sponsor Name:Celgene International II Sàrl (CIS II) | |||||||||||||
Full Title: A Multi-Site, Open-Label Extension Trial of Oral RPC1063 in Relapsing Multiple Sclerosis | |||||||||||||
Medical condition: Relapsing Multiple Sclerosis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) BE (Completed) GB (Completed) ES (Completed) BG (Completed) SK (Completed) GR (Completed) PL (Completed) LV (Completed) EE (Completed) LT (Completed) PT (Completed) SE (Completed) HR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-006033-32 | Sponsor Protocol Number: S308.3.001 | Start Date*: 2006-04-20 |
Sponsor Name:Solvay Pharmaceuticals | ||
Full Title: A Randomized, Double-blind, Placebo Controlled Parallel-group Fixed and Flexible SLV308 Dose Arm Study to Assess Efficacy and Safety of SLV308 Monotherapy in the Treatment of Patients with Early St... | ||
Medical condition: Parkinson's Disease Early Stage | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) SK (Completed) SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-004112-51 | Sponsor Protocol Number: V1512-2PD01 | Start Date*: 2006-11-14 | |||||||||||
Sponsor Name:VERNALIS DEVELOPMENT LIMITED | |||||||||||||
Full Title: A randomised, double-blind, double-dummy, two-period, cross-over study to determine the pharmacokinetics, pharmacodynamics and safety of multiple doses of V1512 effervescent tablets in Parkinson s ... | |||||||||||||
Medical condition: 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: 2010-020769-25 | Sponsor Protocol Number: CECILE | Start Date*: 2010-08-10 | |||||||||||
Sponsor Name:CHU de Poitiers | |||||||||||||
Full Title: Evaluation médico-économique de l’infusion continue intra-duodénale d’une forme gélifiée de levodopa dans le traitement des formes avancées et sévères de maladie de parkinson par l’intermédiaire d’... | |||||||||||||
Medical condition: Parkinson's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-012529-12 | Sponsor Protocol Number: 0827703 | Start Date*: 2009-06-10 | |||||||||||
Sponsor Name:CHU de Toulouse | |||||||||||||
Full Title: A randomised, REQUIP® IR-controlled, n-of-1, multiple crossover, pilot trial of the effect of REQUIP®CR on abnormal daytime somnolence in patients with Parkinson’s Disease | |||||||||||||
Medical condition: parkinson's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-004290-19 | Sponsor Protocol Number: SP873 | Start Date*: 2006-01-25 | |||||||||||
Sponsor Name:Schwarz Biosciences GmbH | |||||||||||||
Full Title: A double-blind, placebo-controlled, parallel group, proof of concept trial to assess the tolerabiltiy, safety and efficacy of rotigotine nasal spray for the acute treatment of 'off' symptoms in sub... | |||||||||||||
Medical condition: advanced-stage, idiopathic Parkinson's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) GB (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005140-89 | Sponsor Protocol Number: TVP-1012-120-TYR | Start Date*: 2006-12-11 | |||||||||||
Sponsor Name:TEVA Pharmaceuticals Industries Ltd | |||||||||||||
Full Title: A PHASE I, DOUBLE BLIND, PLACEBO CONTROLLED, RANDOMIZED (WITHIN EACH GROUP) STUDY TO EVALUATE THE INTERACTION BETWEEN ORALLY ADMINISTERED TYRAMINE HYDROCHLORIDE AND RASAGILINE MESILATE IN HEALTHY S... | |||||||||||||
Medical condition: This postmarketing Phase I study is performed in healthy volunteers. The IMP rasagiline 1mg is indicated for the treatment of Parkinson's Disease (PD). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-004447-11 | Sponsor Protocol Number: VR040/2/008 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Vectura Limited | |||||||||||||
Full Title: A Phase IIb Randomised, Double-Blind, Placebo-Controlled, Parallel-Group Study Investigating the Efficacy and Safety of Apomorphine Inhalation Powder in Patients With “On-Off” or “Wearing-Off” Effe... | |||||||||||||
Medical condition: Unpredictable motor fluctuation or “On-Off” or “Wearing-Off” Effects Fluctuating associated with Idiopathic Parkinson’s Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000678-57 | Sponsor Protocol Number: S308.3.003 | Start Date*: 2007-06-18 | |||||||||||
Sponsor Name:Solvay pharmaceuticals | |||||||||||||
Full Title: A multicenter, randomized, double blind, parallel-group placebo and pramipexole controlled study to assess efficacy and safety of SLV308 monotherapy in the treatment of patients with early stage Pa... | |||||||||||||
Medical condition: Parkinson 's Disease early stage | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) PT (Completed) EE (Completed) LT (Completed) DE (Completed) FR (Completed) NL (Completed) GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000801-64 | Sponsor Protocol Number: BTG001 | Start Date*: 2013-02-09 | |||||||||||
Sponsor Name:University Hospital of North Staffordshire [...] | |||||||||||||
Full Title: A Phase IV Acceptability and Feasibility Trial of the Effects of Medication on Memory in Idiopathic Nondementing Parkinson’s Disease. | |||||||||||||
Medical condition: Idiopathic Parkinson's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000056-42 | Sponsor Protocol Number: SP0919 | Start Date*: 2011-10-07 | |||||||||||
Sponsor Name:UCB Celltech, UK - Registered Branch of UCB Pharma SA | |||||||||||||
Full Title: A MULTI-CENTRE, RANDOMIZED, DOUBLE-BLIND, PLACEBO CONTROLLED STUDY TO EVALUATE THE EFFECTS OF ROTIGOTINE ON SLEEP EFFICIENCY IN PATIENTS WITH ADVANCED PARKINSON’S DISEASE | |||||||||||||
Medical condition: Advanced Parkinson's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-017238-39 | Sponsor Protocol Number: IPX066-B09-06 | Start Date*: 2010-09-15 | |||||||||||
Sponsor Name:Impax Laboratories, Inc., acting through its Impax Pharmaceuticals Division (Impax) | |||||||||||||
Full Title: A Study to Compare IPX066 and Carbidopa/Levodopa/Entacapone (CLE) in Advanced Parkinson’s Disease | |||||||||||||
Medical condition: Idiopathic Parkinson’s Disease (paralysis agitans) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) IT (Completed) BE (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020299-42 | Sponsor Protocol Number: KKS-135 | Start Date*: 2011-08-30 | |||||||||||
Sponsor Name:Philipps-University Marburg | |||||||||||||
Full Title: A randomized, placebo-controlled, double-blind, multi-center trial to assess the disease-modifying potential of transdermal nicotine in early Parkinson's disease in Germany and the USA (NIC-PD) | |||||||||||||
Medical condition: Early PD subjects within 18 months of diagnosis and not expected to require dopamine agonist or levodopa therapy for 1 year, with Hoehn and Yahr stage <2, with stable (>2 months) MAO-B inhibitor th... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-004943-12 | Sponsor Protocol Number: S308.3.010 | Start Date*: 2008-11-24 | |||||||||||
Sponsor Name:Solvay Pharmaceuticals B.V. | |||||||||||||
Full Title: The Rubens Study: A Multicenter, Randomized, Double-blind, Parallel Group, Placebo and Pramipexole Controlled Study to Explore the Efficacy, Tolerability and Safety of Different Doses and Titration... | |||||||||||||
Medical condition: Early Stage Parkinson’s Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001755-36 | Sponsor Protocol Number: 2939117 | Start Date*: 2006-08-09 | |||||||||||
Sponsor Name:Orion Corporation Orion Pharma, FI-02200 Espoo, Finland | |||||||||||||
Full Title: Efficacy and safety of Stalevo in subjects with early wearing-off identified using a screening tool WOQ-9; An open, non-randomised, multinational, multi-centre 6-week direct switch study in levodop... | |||||||||||||
Medical condition: Parkinson’s disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006752-35 | Sponsor Protocol Number: SP889 | Start Date*: 2007-05-09 | |||||||||||
Sponsor Name:Schwarz Biosciences GmbH | |||||||||||||
Full Title: RECOVER: RANDOMIZED EVALUATION OF THE 24-HOUR COVERAGE: EFFICACY OF ROTIGOTINE PHASE 3B, MULTICENTER, MULTINATIONAL, DOUBLE-BLIND, PLACEBO CONTROLLED, 2-ARM TRIAL TO EVALUATE THE EFFECT OF THE 24-H... | |||||||||||||
Medical condition: Parkinson's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) DE (Prematurely Ended) ES (Completed) HU (Completed) IT (Completed) AT (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
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