- Trials with a EudraCT protocol (24)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
24 result(s) found for: Parkinsonian disorders.
Displaying page 1 of 2.
EudraCT Number: 2008-002578-36 | Sponsor Protocol Number: 2008/0817 | Start Date*: 2008-09-10 |
Sponsor Name:CHRU de LILLE | ||
Full Title: Etude d’efficacité et d’acceptabilité d’un traitement cholinergique dans l’apathie parkinsonienne “Cholinergic treatment in Parkinsonian Apathy: ChoPA - I” | ||
Medical condition: Parkinsonian Apathy without dementia and depression in spite of dopaminergic treatment | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-001218-40 | Sponsor Protocol Number: SC12-02 | Start Date*: 2012-05-21 | |||||||||||
Sponsor Name:FONDAZIONE SANTA LUCIA | |||||||||||||
Full Title: EFFICACY OF ROTIGOTINE ON GAIT PERFORMANCE OF PARKINSONIAN PATIENTS | |||||||||||||
Medical condition: Patients suffering for Idiopathic Parkinson’s Disease. H&Y stage > or = 2 with un-satisfactory control by on-going pharmacological therapy (Levodopa, COMT & MAO-inhibitors), characterised by an in... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-002216-25 | Sponsor Protocol Number: PDT409 | Start Date*: 2006-06-26 |
Sponsor Name:Amersham Health, S.A. (filial de GE Healthcare Ltd) | ||
Full Title: Ensayo en fase 4 multicéntrico, aleatorizado, abierto y comparativo para evaluar las modificaciones en el manejo clínico después de una tomografía con DaTSCAN en sujetos con parkinsonismo clínicame... | ||
Medical condition: The subjects included in this trial will have clinically uncertain parkinsonism in a general neurologist setting. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) IT (Completed) DK (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2012-000364-21 | Sponsor Protocol Number: PI1102031 | Start Date*: 2012-11-13 | |||||||||||
Sponsor Name:Fundació Clínic per a la Recerca Biomédica | |||||||||||||
Full Title: FDDNP-PET FOR IN VIVO DIAGNOSIS OF TAUOPATHY IN UNCLASSIFIABLE PARKINSONISM | |||||||||||||
Medical condition: Atypical Parkinsonism | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004145-16 | Sponsor Protocol Number: Z7219K01 | Start Date*: 2019-07-24 | |||||||||||
Sponsor Name:Zambon SpA | |||||||||||||
Full Title: A 12-weeks, multicentre, randomized, double-blind, placebo-controlled, exploratory, pilot study to evaluate the safety and efficacy of safinamide 200 mg once daily, as add-on therapy, in patients w... | |||||||||||||
Medical condition: Parkinsonian variant of Multiple System Atrophy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-010193-38 | Sponsor Protocol Number: IPX066-B08-05 | Start Date*: 2009-06-02 | |||||||||||
Sponsor Name:IMPAX Pharmaceuticals a Division of IMPAX Laboratories, Inc. | |||||||||||||
Full Title: A Placebo-Controlled Study to Evaluate the Safety and Efficacy 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: LT (Completed) EE (Completed) LV (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000122-26 | Sponsor Protocol Number: 125591 | Start Date*: 2020-05-11 | |||||||||||
Sponsor Name:University College London (UCL) | |||||||||||||
Full Title: A Phase IIa, open label, single-site, 48 week randomised controlled trial evaluating the safety and efficacy of Exenatide once-weekly in the treatment of patients with Multiple System Atrophy | |||||||||||||
Medical condition: Multiple System Atrophy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-001092-39 | Sponsor Protocol Number: CAQW051A2209 | Start Date*: 2011-06-29 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A multi-centre, randomized, double-blind, placebo-controlled, parallel-group, multiple oral dose study to assess the efficacy, safety and tolerability of AQW051 in reducing L-dopa induced dyskinesi... | |||||||||||||
Medical condition: L-dopa induced dyskinesias in Parkinson’s patients with moderate to severe L-dopa induced dyskinesias | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000361-11 | Sponsor Protocol Number: RD639/24201 | Start Date*: 2006-06-23 | |||||||||||
Sponsor Name:Fujimoto Pharmaceutical Corporation | |||||||||||||
Full Title: A Proof of Concept Study to Determine the Minimum Effective Dose and to Assess the Efficacy and Safety of Subcutaneous Injections of FPFS-1169 in Parkinson's Disease Patients | |||||||||||||
Medical condition: Treatment of Parkinson's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000373-13 | Sponsor Protocol Number: AMBS-ELTO-201 | Start Date*: 2015-08-18 | |||||||||||
Sponsor Name:Amarantus BioScience Holdings, Inc. | |||||||||||||
Full Title: Phase 2, multicenter, randomized, double-blind, placebo-controlled, four-period cross-over, dose-range finding study to evaluate the safety, tolerability and efficacy of Eltoprazine in the treatmen... | |||||||||||||
Medical condition: Parkinson’s disease levodopa induced dyskinesia (PD-LID) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Temporarily Halted) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002073-30 | Sponsor Protocol Number: CAFQ056A2222 | Start Date*: 2011-11-16 | |||||||||||
Sponsor Name:Novartis Farmaceutica, S.A. | |||||||||||||
Full Title: 12-week, double-blind, placebo-controlled, fixed-dose, multicenter study to evaluate the efficacy and safety of AFQ056 in reducing moderate to severe L-dopa induced dyskinesias in patients with Par... | |||||||||||||
Medical condition: L-dopa induced dyskinesias in patients with Parkinson?s disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
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: 2021-000854-24 | Sponsor Protocol Number: VE-CIP2001/2021 | Start Date*: 2021-12-21 | |||||||||||
Sponsor Name:ALFASIGMA S.P.A. | |||||||||||||
Full Title: Velusetrag for the treatment of Chronic Intestinal Pseudo-Obstruction (CIPO). A multicenter double-blind, placebo-controlled, cross-over, multiple (n=1) trial. | |||||||||||||
Medical condition: Chronic intestinal pseudo-obstruction (CIPO) is a rare, severe condition characterized by an impairment of coordinated propulsive activity in the intestinal tract resulting in a clinical picture si... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) BE (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002678-29 | Sponsor Protocol Number: ANAVEX2-73-PDD-EP-001 | Start Date*: 2019-12-05 | ||||||||||||||||
Sponsor Name:Anavex Life Sciences Corp. | ||||||||||||||||||
Full Title: Open Label Extension Study for Patients with Parkinson’s Disease with Dementia Previously Enrolled in ANAVEX2-73-PDD-001 Study for Continued Safety Assessment | ||||||||||||||||||
Medical condition: Cognition in Parkinson’s Disease with Dementia | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002074-23 | Sponsor Protocol Number: CAFQ056A2223 | Start Date*: 2012-03-20 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: 13-week, double-blind, placebo-controlled, fixed-dose, multicenter study to evaluate the efficacy and safety of modified release AFQ056 in reducing moderate to severe L-dopa induced dyskinesias in ... | |||||||||||||
Medical condition: L-dopa induced dyskinesias in patients with Parkinson's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) HU (Completed) ES (Completed) IT (Completed) SK (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020112-11 | Sponsor Protocol Number: P07037 | Start Date*: 2011-06-29 | |||||||||||
Sponsor Name:Schering-Plough Research Institute, a division of Schering Corporation | |||||||||||||
Full Title: A Phase 3, 12-Week, Double-Blind, Placebo-Controlled Efficacy and Safety Study of Preladenant in Subjects with Moderate to Severe Parkinson’s Disease. (Phase 3; Protocol No. P07037) | |||||||||||||
Medical condition: Parkinson's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) LV (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003053-25 | Sponsor Protocol Number: 1466 | Start Date*: 2012-06-18 | |||||||||||
Sponsor Name:Research and Enterprise Department | |||||||||||||
Full Title: A randomised, double blind, placebo controlled trial to evaluate the effect of Rivastigmine on gait in people with Parkinson’s disease who have fallen. | |||||||||||||
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: 2022-001542-38 | Sponsor Protocol Number: ANVS-22001 | Start Date*: 2023-01-09 |
Sponsor Name:Annovis Bio, Inc. | ||
Full Title: A 6-month prospective, randomized, double-blind, placebo-controlled clinical trial investigating the efficacy, safety, and tolerability of two different doses of buntanetap or placebo in patients w... | ||
Medical condition: Parkinson’s disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) HU (Completed) IT (Completed) PL (Completed) ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-002600-24 | Sponsor Protocol Number: Z7219L02 | Start Date*: 2015-11-03 | |||||||||||
Sponsor Name:Zambon S.P.A. | |||||||||||||
Full Title: A TWO YEAR, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO CONTROLLED STUDY TO EVALUATE THE LONG TERM EFFICACY AND SAFETY OF SAFINAMIDE 100 MG, ONCE DAILY, AS ADD ON THERAPY, IN IDIOPATHIC PARKINSO... | |||||||||||||
Medical condition: Idiopathic Parkinson's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) SE (Prematurely Ended) AT (Prematurely Ended) ES (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000135-14 | Sponsor Protocol Number: PXT-CL17-001 | Start Date*: 2017-05-26 | |||||||||||
Sponsor Name:Prexton Therapeutics B.V. | |||||||||||||
Full Title: A Multi-centre, Double-blind, Randomised, Placebo-controlled, Parallel-arm Phase IIa Trial to Evaluate the Efficacy, Safety and Tolerability of 28-Day Oral Treatment with PXT002331 (foliglurax) in ... | |||||||||||||
Medical condition: Parkinson’s Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) DE (Completed) GB (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
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