- Trials with a EudraCT protocol (38)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
38 result(s) found for: Rasagiline.
Displaying page 1 of 2.
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: 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: 2009-014644-11 | Sponsor Protocol Number: MSA-RAS-202 | Start Date*: 2009-12-08 | |||||||||||
Sponsor Name:Teva Pharmaceutical Industries Ltd | |||||||||||||
Full Title: A Multi-centered, Randomized, Double-blind, Placebo-controlled Clinical Trial to Assess the Efficacy, Safety, and Tolerability of Rasagiline Mesylate 1 mg in Patients with Multiple System Atrophy o... | |||||||||||||
Medical condition: Multiple System Atrophy of the Parkinsonian Subtype | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FR (Completed) ES (Completed) HU (Completed) AT (Completed) NL (Completed) IT (Completed) PT (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-001420-21 | Sponsor Protocol Number: P2B001/003 | Start Date*: 2018-06-18 | |||||||||||
Sponsor Name:Pharma Two B Ltd | |||||||||||||
Full Title: A Phase 3, Twelve-week, Multi-Center, Multinational, Randomized, Double-Blind, Double-Dummy, Parallel Group Study to Determine the Efficacy, Safety and Tolerability of P2B001 Once Daily Compared to... | |||||||||||||
Medical condition: Early Parkinson's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Restarted) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001416-42 | Sponsor Protocol Number: TVP-1012/500 | Start Date*: 2005-09-15 | |||||||||||
Sponsor Name:Teva Pharmaceuticals Industries LtD | |||||||||||||
Full Title: A Multicenter, Double-Blind, Randomized Start, Placebo-Controlled, Parallel-Group Study to Assess Rasagiline as a Disease Modifying Therapy in Early Parkinson’s Disease Subjects | |||||||||||||
Medical condition: Parkinson's Disease | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) HU (Completed) IT (Completed) ES (Completed) AT (Completed) PT (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-013004-31 | Sponsor Protocol Number: RASA-ROPI | Start Date*: 2009-11-02 | |||||||||||
Sponsor Name:UNIVERSITA` DEGLI STUDI DI PARMA | |||||||||||||
Full Title: Early combined prolonged release ropinirole and rasagiline therapy in newly diagnosed patients with Parkinsons disease. A prospective, randomized, parallel groups, long-term follow-up study inc... | |||||||||||||
Medical condition: Patients with Parkinson`s diesease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004482-32 | Sponsor Protocol Number: RAS-ALS | Start Date*: 2013-04-10 | |||||||||||
Sponsor Name:Universitätsklinikum Ulm | |||||||||||||
Full Title: Efficacy, Safety and Tolerability Study of 1 mg Rasagiline in Patients with Amyotrophic Lateral Sclerosis (ALS) Receiving Standard Therapy (Riluzole) | |||||||||||||
Medical condition: Amyotrophic Lateral Sclerosis (ALS) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
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: 2009-015162-57 | Sponsor Protocol Number: P06153 | Start Date*: 2011-03-02 | |||||||||||
Sponsor Name:Schering-Plough Research Institute, a division of Schering Corporation | |||||||||||||
Full Title: A Phase 3, 40-Week, Active-Controlled, Double-Blind, Double-Dummy Extension Study of Preladenant in Subjects With Moderate to Severe Parkinson’s Disease (Phase 3, Protocol No. P06153) | |||||||||||||
Medical condition: Parkinson's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) GB (Prematurely Ended) AT (Prematurely Ended) ES (Prematurely Ended) CZ (Prematurely Ended) LT (Prematurely Ended) IT (Prematurely Ended) LV (Prematurely Ended) NL (Completed) SE (Prematurely Ended) BG (Completed) PT (Prematurely Ended) PL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-007397-28 | Sponsor Protocol Number: 2007-007397-28 | Start Date*: 2008-08-06 |
Sponsor Name:Qualissima | ||
Full Title: Evaluation de la tolérance et de l’acceptabilité de la Rasagiline dans le traitement de la maladie de Parkinson au stade précoce | ||
Medical condition: Maladie de Parkinson idiopathique au stade précoce Maladie de Parkinson, numéro de classification MedDRA 10061536 | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-015161-31 | Sponsor Protocol Number: P04938 | Start Date*: 2010-08-17 | |||||||||||
Sponsor Name:Schering-Plough Research Institute, a division of Schering Corporation | |||||||||||||
Full Title: A Phase 3, 12-Week, Double-Blind, Double-Dummy, Placebo- and Active-Controlled Efficacy and Safety Study of Preladenant in Subjects With Moderate to Severe Parkinson’s Disease (Phase 3; Protocol No... | |||||||||||||
Medical condition: Parkinson's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) GB (Completed) CZ (Completed) FR (Completed) NL (Completed) ES (Completed) AT (Completed) DE (Completed) IT (Completed) SE (Completed) PT (Completed) BG (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-007520-26 | Sponsor Protocol Number: PROSPERA (Rasagiline) | Start Date*: 2010-06-24 | |||||||||||
Sponsor Name:Klinikum der Universität München | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study to assess the Efficacy, Tolerability and Safety of Rasagiline in Subjects with Progressive Supranuclear Palsy (Phase III) | |||||||||||||
Medical condition: Progressive Supranuclear Palsy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004530-33 | Sponsor Protocol Number: 3337541 | Start Date*: 2006-04-12 |
Sponsor Name:Oy Lundbeck | ||
Full Title: Rasagiliinin ja essitalopraamin yhteiskäytön turvallisuus | ||
Medical condition: terveet vapaaehtoiset | ||
Disease: | ||
Population Age: | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-011144-19 | Sponsor Protocol Number: 12962A | Start Date*: 2009-11-19 | |||||||||||
Sponsor Name:LUNDBECK ITALIA | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled study to evaluate if rasagiline can improve depressive symptoms and cognitive function in non-demented, idiopathic Parkinson s disease patients. | |||||||||||||
Medical condition: Subjects will be recruited from the Movement Disorders Outpatient Clinics from academic and hospital institutions in Italy. Only subjects with a BDI-IA score > or = 15 at baseline will be enrolled.... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004400-12 | Sponsor Protocol Number: FIRHSCSP/07/14 | Start Date*: 2007-12-27 | |||||||||||
Sponsor Name:Institut de Recerca de l'Hospital de la santa Creu i Sant Pau | |||||||||||||
Full Title: ENSAYO RANDOMIZADO A DOBLE CIEGO Y CONTROLADO CON PLACEBO DE RASAGILINA EN PACIENTES CON ENFERMEDAD DE PARKINSON Y SINTOMAS DE APATIA | |||||||||||||
Medical condition: Apatía en la Enfermedad de Parkinson | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000973-19 | Sponsor Protocol Number: SWH-MAOB | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:IRCCS SAN RAFFAELE PISANA GESTITO DA SAN RAFFAELE ROMA SRL | |||||||||||||
Full Title: OVERNIGHT SWITCH FROM RASAGILINE TO SAFINAMIDE IN FLUCTUATING PATIENTS WITH PARKINSON’S DISEASE: A TOLERABILITY AND SAFETY STUDY | |||||||||||||
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: 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: 2009-013552-72 | Sponsor Protocol Number: P05664 | Start Date*: 2010-09-07 | |||||||||||
Sponsor Name:Schering-Plough Research Institute, a division of Schering Corporation | |||||||||||||
Full Title: A Phase 3, Double-Blind, Double-Dummy, Placebo- and Active-Controlled Dose-Range-Finding Efficacy and Safety Study of Preladenant in Subjects With Early Parkinson’s Disease (Phase 3 Protocol No. P0... | |||||||||||||
Medical condition: Parkinson's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Prematurely Ended) GB (Prematurely Ended) ES (Prematurely Ended) CZ (Prematurely Ended) HU (Prematurely Ended) DE (Prematurely Ended) SE (Prematurely Ended) IT (Prematurely Ended) BG (Prematurely Ended) PL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005085-30 | Sponsor Protocol Number: TUD-Olfact-035 | Start Date*: 2009-04-06 | |||||||||||
Sponsor Name:Technische Universität Dresden | |||||||||||||
Full Title: Einfluss von Rasagilin auf das Riechvermögen von Patienten mit idiopathischem Parkinson-Syndrom (Reversibility of olfactory loss in patients with Idiopathic Parkinson’s disease following treatme... | |||||||||||||
Medical condition: Idiopathic Parkinson syndrome (IPS), State according to Hoehn & Yahr: maximum III | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003679-31 | Sponsor Protocol Number: 2015_22 | Start Date*: 2016-04-06 |
Sponsor Name:Centre Hospitalier Régional et Universitaire de Lille | ||
Full Title: Conservative iron chelation as a disease-modifying strategy in Parkinson’s disease | ||
Medical condition: De Novo Parkinson’s disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) ES (Ongoing) CZ (Completed) PT (Completed) FR (Completed) NL (Completed) | ||
Trial results: (No results available) |
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