- Trials with a EudraCT protocol (126)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
126 result(s) found for: Dyskinesia.
Displaying page 1 of 7.
EudraCT Number: 2011-004211-23 | Sponsor Protocol Number: PI11-PR-KRYSTKOWIAK | Start Date*: 2011-11-08 | |||||||||||
Sponsor Name:CHU Amiens | |||||||||||||
Full Title: | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-001685-35 | Sponsor Protocol Number: ADT-2022-003 | Start Date*: 2022-12-27 | |||||||||||
Sponsor Name:Adeptio Pharmaceuticals Limited | |||||||||||||
Full Title: Randomized, double-blind, placebo controlled clinical trial of (+)-α-dihydrotetrabenazine in patients with moderate to severe tardive dyskinesia. | |||||||||||||
Medical condition: Tardive dyskinesia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Trial now transitioned) HU (Trial now transitioned) SK (Trial now transitioned) PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-000271-39 | Sponsor Protocol Number: 2022-01 | Start Date*: 2022-09-02 | |||||||||||
Sponsor Name:Adeptio Pharmaceuticals Ltd | |||||||||||||
Full Title: Single-arm, open-label dose titration phase 2 clinical trial of (+)-α-DHTBZ for the treatment of tardive dyskinesia (TD) | |||||||||||||
Medical condition: Tardive dyskinesia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HR (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: 2004-001302-27 | Sponsor Protocol Number: N01142 | Start Date*: 2005-06-10 | |||||||||||
Sponsor Name:UCB S.A. Pharma Sector | |||||||||||||
Full Title: An 8-week exploratory, double-blind, placebo controlled, randomized trial : Evaluation of the efficacy and safety of levetiracetam up to 3000 mg/day (250-500 mg oral tablets in b.i.d. administratio... | |||||||||||||
Medical condition: Tardive dyskinesia usually occurs after prolonged exposure to antipsychotics and is characterized by abnormal choreiform, athetoic, choreathetoic or rhythmic involuntary movements. The localizatio... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003458-18 | Sponsor Protocol Number: IRL790C003 | Start Date*: 2017-12-19 | |||||||||||
Sponsor Name:Integrative Research Laboratories AB (IRLAB) | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled, phase IIA study evaluating the efficacy and tolerability of IRL790 in Parkinson's disease dyskinesia | |||||||||||||
Medical condition: Parkinson's disease dyskinesia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003739-20 | Sponsor Protocol Number: ADS-AMT-PD302 | Start Date*: 2015-04-23 | |||||||||||
Sponsor Name:Adamas Pharmaceuticals, Inc. | |||||||||||||
Full Title: Open-Label Safety Study of ADS-5102 (Amantadine HCl) Extended Release Capsules for the Treatment of Levodopa-Induced Dyskinesia | |||||||||||||
Medical condition: Treatment of levodopa-induced dyskinesia in subjects with Parkinson's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) AT (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004664-58 | Sponsor Protocol Number: BESTCILIA-WP5 | Start Date*: 2014-08-26 | |||||||||||
Sponsor Name:Paediatric Pulmonary Service, Department of Paediatrics and Adolescent Medicine, Rigshospitalet, Copenhagen, Denmark | |||||||||||||
Full Title: RANDOMIZED CONTROLLED TRIAL (RCT) TO DETERMINE THE EFFICACY AND SAFETY OF AZITHROMYCIN (AZN) MAINTENANCE THERAPY FOR 6 MONTHS IN SUBJECTS WITH PCD - A DOUBLE-BLIND, PARALLEL GROUP STUDY | |||||||||||||
Medical condition: Primary ciliary dyskinesia (PCD) | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) DK (Prematurely Ended) GB (Prematurely Ended) NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003738-24 | Sponsor Protocol Number: ADS-AMT-PD304 | Start Date*: 2015-04-23 | |||||||||||
Sponsor Name:Adamas Pharmaceuticals, Inc. | |||||||||||||
Full Title: ADS-5102 (Amantadine HCl) Extended Release Efficacy and Safety Study in Parkinson's Disease Patients with Levodopa-Induced Dyskinesia | |||||||||||||
Medical condition: Treatment of levodopa-induced dyskinesia in subjects with Parkinson's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022517-25 | Sponsor Protocol Number: ADX48621-201 | Start Date*: 2011-05-30 | |||||||||||
Sponsor Name:Addex Pharma SA | |||||||||||||
Full Title: Phase 2, randomized, double-blind, placebo-controlled, parallel group, multicenter study to evaluate the safety, tolerability and efficacy of ADX48621 in the treatment of levodopa induced dyskinesi... | |||||||||||||
Medical condition: Levodopa induced dyskinesia in Parkinson's disease patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003415-19 | Sponsor Protocol Number: JM-010CS03 | Start Date*: 2018-10-31 |
Sponsor Name:Contera Pharma | ||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study in Parkinson’s Disease Patients With Moderate to Severe Dyskinesia to Assess the Efficacy and Safety/Tolerability of Two Dose Co... | ||
Medical condition: Parkinson’s Disease Patients With Moderate to Severe Dyskinesia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Restarted) IT (Completed) SK (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-001593-10 | Sponsor Protocol Number: EMR 62225-018 | Start Date*: 2004-12-02 |
Sponsor Name:MERCK S.P.A. | ||
Full Title: A double-blind, placebo-controlled, multicenter, multinational Phase III study to evaluate the safety and efficacy of Sarizotan HCl 1 mg b.i.d. in patients with Parkinson's disease suffering from t... | ||
Medical condition: Treatment-Associated Dyskinesia in Parkinson's Disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Completed) GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-006053-22 | Sponsor Protocol Number: NLX-112-DYS-101 | Start Date*: 2021-09-22 |
Sponsor Name:Neurolixis SAS | ||
Full Title: A Randomized, Double-blind, Placebo-controlled Study to Assess the Safety, Tolerability and Preliminary Efficacy of NLX-112 versus Placebo in Levodopa-induced Dyskinesia in Parkinson’s Disease | ||
Medical condition: Parkinson´s disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-001594-25 | Sponsor Protocol Number: EMR62225-019 | Start Date*: 2004-12-30 |
Sponsor Name:Merck KGaA | ||
Full Title: A double-blind, placebo-controlled, multicenter, multinational Phase III study to evaluate the safety and efficacy of Sarizotan HCl 1 mg b.i.d. in patients with Parkinson's disease suffering from t... | ||
Medical condition: Treatment-Associated Dyskinesia in Parkinson's Disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) ES (Completed) AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-001403-23 | Sponsor Protocol Number: M15-535 | Start Date*: 2017-02-22 | |||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
Full Title: An Open-label, Randomized 12 Week Study Comparing Efficacy of Levodopa-Carbidopa Intestinal Gel/Carbidopa-Levodopa Enteral Suspension and Optimized Medical Treatment on Dyskinesia in Subjects with ... | |||||||||||||
Medical condition: Dyskinesia in advanced Parkinson's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) SK (Completed) GR (Completed) ES (Completed) HU (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-000444-84 | Sponsor Protocol Number: EMR62225-030 | Start Date*: 2005-06-22 |
Sponsor Name:Merck KGaA | ||
Full Title: An open-label, multicenter, multinational Phase III follow-up study to investigate the long-term safety and efficacy of Sarizotan HCl 1 mg b.i.d. in patients with Parkinson's disease suffering from... | ||
Medical condition: Treatment-Associated Dyskinesia in Parkinson's Disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) FI (Prematurely Ended) GB (Completed) IT (Prematurely Ended) ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-002010-41 | Sponsor Protocol Number: IRL790C005 | Start Date*: 2020-12-22 | |||||||||||
Sponsor Name:Integrative Research Laboratories Sweden AB (IRLAB) | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled phase IIB study evaluating the efficacy of mesdopetam on DAILY on-time without troublesome dyskinesia in patients with Parkinson’s disease | |||||||||||||
Medical condition: Parkinson's disease dyskinesia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
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: 2007-002467-27 | Sponsor Protocol Number: 2007 Neuro 12 | Start Date*: 2008-01-24 | |||||||||||||||||||||
Sponsor Name:Salford Royal NHS Foundation Trust | |||||||||||||||||||||||
Full Title: Antidyskinetic Properties of Topiramate: A Double-Blind, Placebo-Controlled Trial in Patients with Parkinson's Disease and Levodopa-Induced Dyskinesias | |||||||||||||||||||||||
Medical condition: Patients with idiopathic Parkinson's disease and levodopa-induced dyskinesias | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-001890-15 | Sponsor Protocol Number: SD-809-C-18 | Start Date*: 2014-11-12 |
Sponsor Name:Auspex Pharmaceuticals, Inc. | ||
Full Title: A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY OF SD-809 (DEUTETRABENAZINE) FOR THE TREATMENT OF MODERATE TO SEVERE TARDIVE DYSKINESIA | ||
Medical condition: Tardive Dyskinesia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) PL (Completed) SK (Completed) | ||
Trial results: View results |
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