- Trials with a EudraCT protocol (84)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
84 result(s) found for: Carbidopa.
Displaying page 1 of 5.
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: 2015-004507-23 | 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: 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: 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: 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: 2008-001123-62 | Sponsor Protocol Number: Droxidopa FMS 201 | Start Date*: 2009-02-13 | |||||||||||
Sponsor Name:Chelsea Therapeutics Inc. | |||||||||||||
Full Title: A PHASE II, MULTI-CENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, DOSE-RESPONSE, STUDY TO ASSESS THE CLINICAL BENEFIT OF DROXIDOPA AND DROXIDOPA/CARBIDOPA IN SUBJECTS WITH FIBROMYALGIA | |||||||||||||
Medical condition: Treatment of pain associated with fibromyalgia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (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: 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: 2007-003134-42 | Sponsor Protocol Number: CELC200AUS15 | Start Date*: 2008-06-19 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A 12-Week, Multi-center, Randomized, Prospective, Open-Label, Blinded Rater, Crossover Study of the Effects of Immediate-Release Carbidopa/Levodopa Versus Stalevo® on Markers of Event-Related Poten... | |||||||||||||
Medical condition: Idiopathic Parkinson’s disease and end-of-dose wearing off. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003513-24 | Sponsor Protocol Number: IN11004OLE | Start Date*: 2016-05-24 | |||||||||||
Sponsor Name:Intec Pharma, Ltd. | |||||||||||||
Full Title: An Open-Label, Multi-Center, Follow-Up Study Designed to Evaluate the Long-Term Effects of AP-CD/LD in Fluctuating Parkinson's Disease Subjects who Completed Study IN 11 004 | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Prematurely Ended) SK (Prematurely Ended) GB (Prematurely Ended) ES (Prematurely Ended) DE (Completed) BG (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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) |
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: 2010-022915-21 | Sponsor Protocol Number: 2939136 | Start Date*: 2011-01-10 | |||||||||||
Sponsor Name:Orion Corporation | |||||||||||||
Full Title: Duration of motor response after administration of experimental levodopa/carbidopa/entacapone treatment regimens compared to standard treatment (Stalevo®); a randomised, double-blind, crossover, mu... | |||||||||||||
Medical condition: Parkinson's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) SE (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: 2018-004156-37 | Sponsor Protocol Number: ND0612-317 | Start Date*: 2020-05-18 | |||||||||||
Sponsor Name:NeuroDerm Ltd. | |||||||||||||
Full Title: A multicenter, randomized, active-controlled, double-blind, double-dummy, parallel group clinical trial, investigating the efficacy, safety, and tolerability of continuous subcutaneous ND0612 infus... | |||||||||||||
Medical condition: Parkinson's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Ongoing) GB (GB - no longer in EU/EEA) CZ (Trial now transitioned) FR (Trial now transitioned) HU (Prematurely Ended) AT (Trial now transitioned) ES (Ongoing) PT (Trial now transitioned) NL (Ongoing) SK (Trial now transitioned) BE (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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: 2018-002233-37 | Sponsor Protocol Number: IPX203-B16-02 | Start Date*: 2019-03-18 | |||||||||||||||||||||
Sponsor Name:Impax Laboratories, LLC | |||||||||||||||||||||||
Full Title: A randomized controlled study to compare the safety and efficacy of IPX203 with immediate-release carbidopa-levodopa in Parkinson's disease patients with motor fluctuations. | |||||||||||||||||||||||
Medical condition: Parkinson's disease | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: CZ (Completed) DE (Completed) GB (GB - no longer in EU/EEA) PL (Completed) IT (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: 2005-000434-21 | Sponsor Protocol Number: LP1 | Start Date*: 2005-06-15 |
Sponsor Name:Kognitive Neurologie, Institut für Medizin, Forschungszentrum Jülich | ||
Full Title: Neurochemische Modulation von Exekutiv- und Gedächtnisfunktionen | ||
Medical condition: Progressive cognitive decline in physiological aging | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
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 |
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