- Trials with a EudraCT protocol (31)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
31 result(s) found for: Decarboxylase inhibitor.
Displaying page 1 of 2.
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: 2006-002192-40 | Sponsor Protocol Number: periodld001 | Start Date*: 2006-07-13 |
Sponsor Name:Zsolt Lohinai DMD PhD | ||
Full Title: New treatment of periodontitis by inhibition of lysine decarboxilase enzyme | ||
Medical condition: healthy volunteers | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-005848-21 | Sponsor Protocol Number: M11-352 | Start Date*: 2013-12-18 | |||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
Full Title: A Randomized, Multicountry, Multicenter, Double-Blind, Parallel, Placebo-Controlled Study of the Effects of Atrasentan on Renal Outcomes in Subjects with Type 2 Diabetes and Nephropathy SONAR: Stud... | |||||||||||||
Medical condition: Diabetic Nephropathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) DE (Prematurely Ended) CZ (Prematurely Ended) BE (Prematurely Ended) GB (Completed) IE (Completed) PT (Prematurely Ended) DK (Prematurely Ended) NL (Prematurely Ended) IT (Prematurely Ended) GR (Completed) SK (Prematurely Ended) FI (Prematurely Ended) ES (Prematurely Ended) PL (Prematurely Ended) AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000726-78 | Sponsor Protocol Number: SPD488-401 | Start Date*: 2004-12-02 |
Sponsor Name:Shire Pharmaceuticals Group plc | ||
Full Title: A 24 Week Randomised Double Blind Placebo Controlled Study to Evaluate the Atrophogenic Potential of Eflornithine in the Treatment of Women with Excessive Facial Hair | ||
Medical condition: Facial Hirsutism in Women | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-021860-13 | Sponsor Protocol Number: BIA-91067-301 | Start Date*: 2010-11-11 | |||||||||||
Sponsor Name:BIAL - Portela & Ca, S.A. | |||||||||||||
Full Title: EFFICACY AND SAFETY OF BIA 9-1067 IN IDIOPATHIC PARKINSON’S DISEASE PATIENTS WITH “WEARING-OFF” PHENOMENON TREATED WITH LEVODOPA PLUS A DOPA DECARBOXYLASE INHIBITOR (DDCI): A DOUBLE-BLIND, RANDOMIS... | |||||||||||||
Medical condition: Adjunct to levodopa (L-DOPA)/DDCI for use in patients with Parkinson’s disease (PD) and end-of-dose motor fluctuations. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) LT (Completed) AT (Completed) LV (Completed) DE (Completed) ES (Completed) PT (Completed) CZ (Completed) SK (Completed) BG (Completed) RO (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000577-29 | Sponsor Protocol Number: S187.3.001 | Start Date*: 2007-04-27 | |||||||||||
Sponsor Name:Abbott Products, Inc (Abbott Products Inc. is part of the parent company, Abbott Laboratories) | |||||||||||||
Full Title: A Randomized, Double-Blind, Double-Dummy, Efficacy, Safety and Tolerability Study Levodopa - Carbidopa Intestinal Gel in Levodopa-Responsive Parkinson’s Subjects Receiving Optimized Treatments with... | |||||||||||||
Medical condition: Treatment of levodopa-responsive Parkinson's subjects with severe motor fluctuations. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
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: 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: 2006-004112-51 | 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: 2015-002571-24 | Sponsor Protocol Number: 15/0118 | Start Date*: 2016-10-14 |
Sponsor Name:Joint Research Office | ||
Full Title: A Phase IIA Prospective, Single-Centre, Open Label Clinical Trial to Evaluate the Safety, Tolerability and Pharmacodynamic Effects of Ambroxol in Patients with Parkinson Disease: Ambroxol in Diseas... | ||
Medical condition: Parkinson disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-005146-39 | Sponsor Protocol Number: P04501 | Start Date*: 2006-09-14 | |||||||||||
Sponsor Name:Schering Plough Research Institute | |||||||||||||
Full Title: A Phase-2, 12-week, Double-Blind, Dose-Finding, Placebo-Controlled Study to Assess the Efficacy and Safety of a range of SCH 420814 Doses 1 mg BID, 2 mg BID, 5 mg BID and Possibly 10 mg BID in Su... | |||||||||||||
Medical condition: Moderate to severe Parkinson s disease with motor fluctuation and dyskinesias. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001717-42 | Sponsor Protocol Number: P05175 | Start Date*: 2007-10-25 |
Sponsor Name:Schering Plough Research Institute | ||
Full Title: A Phase 2, 36 Week, Open-Label, Uncontrolled Safety Follow-Up Study Assessing SCH 420814 5 mg BID | ||
Medical condition: Patients with Moderate to Severe Parkinson's Disease Experiencing Motor Fluctuations and Dyskinesias | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-002855-41 | Sponsor Protocol Number: ANeED | Start Date*: 2021-01-12 | |||||||||||
Sponsor Name:Helse Fonna | |||||||||||||
Full Title: A phase IIa multicentre randomized controlled double blind clinical trial to demonstrate clinical efficacy on cognitive, neuropsychiatric and functional outcomes of Ambroxol in New and Early patien... | |||||||||||||
Medical condition: Dementia with Lewy Bodies (DLB) and mild cognitive impairment (MCI) due to Lewy Body Disease (DLB-MCI) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-006004-16 | Sponsor Protocol Number: 03PDE2020 | Start Date*: 2021-07-16 |
Sponsor Name:Celon Pharma S.A. | ||
Full Title: Phase II, Double blind, Randomized, Placebo controlled, Parallel group, Trial to Explore the Potential Anti-dyskinetic Properties of CPL500036 (PDE10A inhibitor) in Patients with Parkinson's Diseas... | ||
Medical condition: Levodopa-induced dyskinesia in Parkinson's Disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: PL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-004892-11 | Sponsor Protocol Number: SteP-on | Start Date*: 2021-04-22 | |||||||||||
Sponsor Name:OSPEDALE SANTA MARIA DELLA MISERICORDIA | |||||||||||||
Full Title: A randomized, double-blind, placebo controlled, multicentre study to evaluate the effect of safinamide on freezing of gait (FOG) in mid- to late-stage fluctuating PD patients | |||||||||||||
Medical condition: • Subjects of both genders over 18 years of age, with a clinical diagnosis of idiopathic PD • A Modified Hoehn and Yahr stage of = 4 in the “off” state; • A stable (4 weeks since last modification)... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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: 2020-005011-52 | Sponsor Protocol Number: BIA-91067-303 | Start Date*: 2021-05-12 | |||||||||||
Sponsor Name:BIAL – Portela & Cª, S.A. | |||||||||||||
Full Title: A Phase III, Double-Blind, Randomized, Placebo-Controlled and Parallel Group Study to Evaluate the Efficacy and Safety of Opicapone, as Add on to Stable Levodopa (L-DOPA) Plus a Dopa Decarboxylase ... | |||||||||||||
Medical condition: Early Idiopathic Parkinson’s disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) BG (Completed) PT (Completed) FR (Completed) BE (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000669-21 | Sponsor Protocol Number: 1218-0091 | Start Date*: 2018-04-02 | |||||||||||
Sponsor Name:Unilfarma - União Internacional de Lab. Farmacêuticos, Lda. | |||||||||||||
Full Title: A double-blind, randomised, placebo-controlled, parallel group trial to evaluate the efficacy and safety of empagliflozin and linagliptin over 26 weeks, with a double-blind active treatment safety ... | |||||||||||||
Medical condition: Diabetes Mellitus Type 2 | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: PT (Prematurely Ended) Outside EU/EEA DE (Completed) NL (Completed) GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-001793-24 | Sponsor Protocol Number: SCO/BIA-3202-202 | Start Date*: 2006-07-31 | |||||||||||
Sponsor Name:BIAL - Portela & Cª, SA | |||||||||||||
Full Title: A MULTICENTRE, DOUBLE-BLIND, RANDOMIZED, ACTIVE- AND PLACEBO-CONTROLLED TRIAL TO INVESTIGATE THE EFFICACY AND TOLERABILITY OF NEBICAPONE IN PARKINSON’S DISEASE PATIENTS WITH “WEARING-OFF” PHENOMENO... | |||||||||||||
Medical condition: Patients with idiopathic Parkinson’s disease (PD) and with end-of-dose deterioration ("wearing-off") phenomenon although currently treated with levodopa/DDCI. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) PT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004912-39 | Sponsor Protocol Number: B7601003 | Start Date*: 2016-06-14 | |||||||||||
Sponsor Name:Pfizer, Inc. | |||||||||||||
Full Title: A 15-WEEK, PHASE 2, DOUBLE BLIND, RANDOMIZED, PLACEBO-CONTROLLED, DOSE RANGING STUDY TO INVESTIGATE THE EFFICACY, SAFETY AND TOLERABILITY OF PF-06649751 IN SUBJECTS WITH MOTOR FLUCTUATIONS DUE TO P... | |||||||||||||
Medical condition: Parkinson's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
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