- Trials with a EudraCT protocol (188)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
188 result(s) found for: Levodopa test.
Displaying page 1 of 10.
EudraCT Number: 2015-004507-23 | Sponsor Protocol Number: 3112004 | Start Date*: 2016-03-15 |
Sponsor Name:Orion Corporation | ||
Full Title: Efficacy and safety of ODM-104 compared to a standard combination (Stalevo); a randomised, double-blind, crossover proof-of-concept study in patients with Parkinson's disease and end-of-dose wearin... | ||
Medical condition: Parkinson's disease (PD) patients with end-of-dose wearing-off (motor fluctuations) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: LV (Completed) DE (Completed) HU (Completed) FI (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-005033-11 | Sponsor Protocol Number: SRx-501-01 | Start Date*: 2008-03-27 |
Sponsor Name:CombinatoRx, Inc | ||
Full Title: A Comparison Of The Safety And Bioavailability Of Modified-Release Formulations Of Levodopa-Carbidopa In Subjects With Parkinson’s Disease | ||
Medical condition: Patients with Parkinson's Disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-003512-20 | Sponsor Protocol Number: IN11004 | Start Date*: 2016-05-09 | |||||||||||
Sponsor Name:Intec Pharma, Ltd. | |||||||||||||
Full Title: A Phase III, Multicenter, Randomized, Double-Blind, Double-Dummy, Active-Controlled Study Comparing the Efficacy and Safety of Gastric Retentive, Controlled Release Accordion Pill™ Carbidopa/Levodo... | |||||||||||||
Medical condition: Parkinson's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Prematurely Ended) GB (Completed) SK (Completed) ES (Completed) PL (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004985-41 | Sponsor Protocol Number: DYSK-PD-2007 | Start Date*: 2007-11-29 |
Sponsor Name:Department of Neuroscience, neurology | ||
Full Title: Different dyskinesias in Parkinson's disease and their relation to levodopa pharmacokinetics | ||
Medical condition: Parkinson's disease, G20.9. Different dyskinesias related to advanced Parkinson's disease will be investigated. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-000680-28 | Sponsor Protocol Number: CELC200AES03 | Start Date*: 2006-07-07 |
Sponsor Name:NOVARTIS FARMACEUTICA, S.A | ||
Full Title: Estudio multicéntrico, doble ciego, aleatorizado y de tres meses de seguimiento para evaluar la eficacia de levodopa/carbidopa/entacapona frente a levodopa/carbidopa en pacientes con enfermedad de ... | ||
Medical condition: Enfermedad de Parkinson (Parkinson Disease) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-003869-72 | Sponsor Protocol Number: BIA-91067-201 | Start Date*: 2008-10-03 | |||||||||||
Sponsor Name:Bial - Portela & Cª, S.A. | |||||||||||||
Full Title: A DOUBLE-BLIND, RANDOMISED, PLACEBO-CONTROLLED, CROSS-OVER STUDY TO INVESTIGATE THE TOLERABILITY AND EFFECT OF THREE SINGLE-DOSE REGIMENS OF BIA 9-1067 ON THE LEVODOPA PHARMACOKINETICS, MOTOR RESPO... | |||||||||||||
Medical condition: Parkinson | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022200-46 | Sponsor Protocol Number: 2939135 | Start Date*: 2011-05-13 | |||||||||||
Sponsor Name:Orion Corporation | |||||||||||||
Full Title: Efficacy and safety of ODM-101 compared to a standard combination (Stalevo®); a randomised, double-blind, crossover, proof of concept study in patients with Parkinson’s disease and end-of-dose moto... | |||||||||||||
Medical condition: Parkinson's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) LV (Completed) LT (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-004129-89 | Sponsor Protocol Number: Motor-Neuromod_01, Part I-III | Start Date*: 2005-09-19 |
Sponsor Name:Universitätsklinikum Münster | ||
Full Title: Potentiation of procedural motor learning by pharmacological neuromodulation and brain stimulation | ||
Medical condition: Healthy volunteers Patients in the chronic stage (> 1 year) after stroke | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2010-019396-29 | Sponsor Protocol Number: LAMP-PD | Start Date*: 2010-05-18 |
Sponsor Name:AZIENDA OSPEDALIERO-UNIVERSITARIA POLICLINICO-VITTORIO EMANUELE | ||
Full Title: Levodopa Administration Modalities and Pramipexole in Parkinson's Disease (LAMP-PD study) A multicenter, randomized, four parallel groups, active-controlled, open-label study to evaluate the risk o... | ||
Medical condition: Patients with idiopathic Parkinson's Disease. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-001209-95 | Sponsor Protocol Number: IN18001 | Start Date*: 2018-07-05 | |||||||||||
Sponsor Name:INTEC PHARMA LTD | |||||||||||||
Full Title: An open-label Phase 2 study to assess the pharmacokinetics of Accordion Pill¿ Carbidopa-Levodopa compared to immediate release carbidopa-levodopa in patients with Parkinson¿s disease | |||||||||||||
Medical condition: Parkinson's Disease (PD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-000185-12 | Sponsor Protocol Number: CELC200A2401 / 2939107 | Start Date*: 2004-09-21 | |||||||||||
Sponsor Name:Orion Corporation, ORION PHARMA | |||||||||||||
Full Title: A long term, double-blind, randomized, parallel-group, carbidopa/levodopa controlled, multi-center study to evaluate the effect of Stalevo® in patients with Parkinson’s disease requiring initiation... | |||||||||||||
Medical condition: Parkinson's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) SE (Completed) AT (Completed) GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001032-72 | Sponsor Protocol Number: CELC200A2305 | Start Date*: 2006-03-23 |
Sponsor Name:Novartis Pharma AG | ||
Full Title: A 39-week randomized, double-blind, parallel group, multicenter study to evaluate the effect of fixed dose Stalevo 100 (t.i.d.) vs. immediate release carbidopa/levodopa (t.i.d.) in Parkinson's dise... | ||
Medical condition: Parkinson disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: PT (Completed) CZ (Completed) IT (Completed) | ||
Trial results: View results |
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: 2009-012897-12 | Sponsor Protocol Number: BIA-91067-202 | Start Date*: 2009-12-08 | |||||||||||
Sponsor Name:BIAL-Portela & Ca, SA | |||||||||||||
Full Title: A double-blind, randomised, placebo-controlled study to investigate the tolerability and the effect of three multiple-dose regimens of BIA 9-1067 on the levodopa pharmacokinetics, catechol-0-methyl... | |||||||||||||
Medical condition: Parkinson’s Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-002496-14 | Sponsor Protocol Number: 2939121 | Start Date*: 2007-11-05 | |||||||||||
Sponsor Name:Orion Corporation Orion Pharma | |||||||||||||
Full Title: Effects of single doses of Stalevo 200 and levodopa/carbidopa 200/50 mg on striatal 11C-raclopride binding potential in Parkinson’s disease patients with wearing-off symptoms. An open, randomised, ... | |||||||||||||
Medical condition: Parkinson’s disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Prematurely Ended) | |||||||||||||
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: 2009-017416-33 | Sponsor Protocol Number: 001.001 | Start Date*: 2010-01-18 | |||||||||||
Sponsor Name:Clinical research lab for neurodegeneration, Dept. of Neurology, St. Josef-Hospital, Ruhr-University | |||||||||||||
Full Title: Standardized clinical trial on the application of Levodopa (LD) / Carbidopa (CD) to patients with Parkinson disease vs LD / CD and Entacapon (EN) vs LD / CD and Tolcapon (TO) concerning the paramet... | |||||||||||||
Medical condition: Male and female patients with Parkinson´s disease meeting UKPDS criteria | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-000686-16 | Sponsor Protocol Number: CHDR1953 | Start Date*: 2020-03-26 | |||||||||||
Sponsor Name:Centre for Human Drug Research | |||||||||||||
Full Title: Randomized, double-blind, placebo-controlled crossover study to validate finger tapping tasks for the quantification of levodopa/carbidopa effects in Parkinson’s Disease patients. | |||||||||||||
Medical condition: Parkinson's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-002964-90 | Sponsor Protocol Number: 27919 | Start Date*: 2011-05-05 | |||||||||||
Sponsor Name:Newron Pharmaceuticals SpA | |||||||||||||
Full Title: A phase III, double-blind, placebo-controlled, randomised trial to determine the efficacy and safety of a dose range of 50 to 100 mg/day of safinamide, as add-on therapy, in subjects with idiopathi... | |||||||||||||
Medical condition: Idiopathic Parkinson's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) FI (Prematurely Ended) FR (Completed) HU (Completed) ES (Completed) NL (Completed) EE (Completed) AT (Completed) SK (Completed) DE (Completed) GB (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002780-17 | Sponsor Protocol Number: ND0612-315 | Start Date*: 2018-05-21 | |||||||||||
Sponsor Name:NeuroDerm Ltd. | |||||||||||||
Full Title: A Pivotal, Open-Label, Randomized, Crossover, Four Sequences Study in Male and Female Patients with Advanced Parkinson’s Disease to Assess the Relative Bioavailability of Levodopa Administered as N... | |||||||||||||
Medical condition: Parkinson’s Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) FR (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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