- Trials with a EudraCT protocol (41)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
41 result(s) found for: Apomorphine.
Displaying page 2 of 3.
EudraCT Number: 2006-004582-33 | Sponsor Protocol Number: VR040/2/002 | Start Date*: 2006-11-03 |
Sponsor Name:Vectura Group plc | ||
Full Title: A Randomised, Double-Blind, Placebo-Controlled, Parallel-Group, Dose-Escalating Study Investigating the Efficacy and Safety of VR040 in the Treatment of Unpredictable “Off” or End-of-Dose “Wearing ... | ||
Medical condition: Hypomobility (off or freezing) episodes associated with advanced Parkinson's disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-005476-32 | Sponsor Protocol Number: VR004/008 | Start Date*: 2006-02-02 |
Sponsor Name:Vectura Group plc | ||
Full Title: A Phase IIb, Randomised, Double-Blind, Placebo Controlled, Dose Finding Study Assessing the Haemodynamic Safety and "At Home" Efficacy of Inhaled VR004 in patients with Erectile Dysfunction (ED). | ||
Medical condition: Erectile dysfunction | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-005814-31 | Sponsor Protocol Number: ND0612H-012 | Start Date*: 2016-08-29 | |||||||||||
Sponsor Name:NeuroDerm Ltd. | |||||||||||||
Full Title: A multicenter, international, open-label, safety study of ND0612, a solution of levodopa/carbidopa delivered via a pump system as a continuous subcutaneous infusion in subjects with advanced Parkin... | |||||||||||||
Medical condition: Subjects with advanced Parkinson's disease | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Trial now transitioned) DE (Ongoing) FR (Trial now transitioned) CZ (Completed) PL (Trial now transitioned) HU (Prematurely Ended) ES (Completed) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-000431-22 | Sponsor Protocol Number: CLLLN | Start Date*: 2005-03-10 | |||||||||||
Sponsor Name:AZIENDA SANITARIA OSPEDALIERA "S. GIOVANNI BATTISTA DI TORINO" | |||||||||||||
Full Title: VALUTATION OF PLACEBO EFFECT AFTER CONDITIONING WITH APOMORPHINE AND WITHOUT PHARMACOLOGICAL CONDITIONING ON THE RIGIDITY AND ELECTRICAL ACTIVITY OF NEURONS OF SUBTHALAMIC NUCLEUS IN PARKINSON PATI... | |||||||||||||
Medical condition: THE TOPICAL INVESTIGATION IS THE BASE OF PATOLOGY | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-002321-23 | Sponsor Protocol Number: V1ComplexitDOC | Start Date*: 2022-03-21 |
Sponsor Name:University of Liège | ||
Full Title: Complexity-enhancing drugs to treat disorders of consciousness (DoC): a ketamine study | ||
Medical condition: Disorders of consciousness as Unresponsive Wakefulness Syndrome (UWS) and Minimally Conscious State (MCS) after a coma due to acquired brain injury. Patients who emerged from the minimally consciou... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2021-006486-38 | Sponsor Protocol Number: ComplexitDOC_PSI | Start Date*: 2022-08-17 |
Sponsor Name:University of Liege | ||
Full Title: Complexity-enhancing drugs to treat disorders of consciousness (DoC): a psilocybin study | ||
Medical condition: Disorders of consciousness as unresponsive wakefulness syndrome (UWS) and minimally conscious state (MCS) after a coma due to acquired brain injury. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Prematurely Ended) | ||
Trial results: (No results available) |
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 | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000181-37 | Sponsor Protocol Number: CVT-301-002 | Start Date*: 2012-04-25 | |||||||||||
Sponsor Name:Civitas Therapeutics, Inc. | |||||||||||||
Full Title: A Randomized, Placebo-Controlled Phase 2 Study of the Safety, Pharmacokinetics, and Pharmacodynamics of CVT-301 (Levodopa Inhalation Powder) in Patients with Parkinson’s Disease and Motor Response ... | |||||||||||||
Medical condition: Parkinson's Disease | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005078-39 | Sponsor Protocol Number: ND0612H-006 | Start Date*: 2016-09-21 | |||||||||||
Sponsor Name:NeuroDerm Ltd. | |||||||||||||
Full Title: A multicenter, parallel-group, rater-blinded, randomized clinical study investigating the efficacy, safety, tolerability and pharmacokinetics of 2 dosing regimens of ND0612H, a solution of levodopa... | |||||||||||||
Medical condition: Subjects with advanced Parkinson's disease | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005822-31 | Sponsor Protocol Number: CVT-301-003 | Start Date*: 2013-04-18 | |||||||||||
Sponsor Name:Civitas Therapeutics, Inc. | |||||||||||||
Full Title: A Phase 2b, Randomized, Double-blind, Placebo-controlled Study Investigating the Efficacy and Safety of Inhaled CVT 301 (Levodopa Inhalation Powder) in Parkinson’s Disease Patients With Motor Respo... | |||||||||||||
Medical condition: Parkinson's Disease | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-004464-69 | Sponsor Protocol Number: VR004/003 | Start Date*: 2005-03-22 | |||||||||||
Sponsor Name:vectura group plc | |||||||||||||
Full Title: A Home Based Phase IIb, Multi-centre, Randomised, Double-Blind, Placebo Controlled, Dose Finding Parallel Group Study to explore the Optimal Dose of Inhaled VR004 in Patients with Erectile Dysfunct... | |||||||||||||
Medical condition: erectile dysfunction | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: GB (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 | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-018650-12 | Sponsor Protocol Number: 0930303 | Start Date*: 2010-07-13 | |||||||||||
Sponsor Name:CHU de Toulouse | |||||||||||||
Full Title: Evaluation du système noradrénergique dans l’altération de la perception douloureuse chez le patient Parkinsonien | |||||||||||||
Medical condition: maladie de Parkinson | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001651-31 | Sponsor Protocol Number: 1.0 | Start Date*: 2017-11-30 |
Sponsor Name:Newcastle upon Tyne Hospitals NHS Foundation Trust | ||
Full Title: EMPOWER: EMesis in Pregnancy - Ondansetron With mEtoclopRamide. | ||
Medical condition: Nausea and Vomiting in pregnancy Hyperemesis gravidarum | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
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 | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: RO (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 | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-018137-37 | Sponsor Protocol Number: 09/0391 | Start Date*: 2010-04-14 | |||||||||||
Sponsor Name:University College London | |||||||||||||
Full Title: An open label, single site, 12 month, Phase II, randomised controlled trial evaluating the safety and efficacy of Exendin-4 (Exenatide) in the treatment of patients with moderate severity Parkinson... | |||||||||||||
Medical condition: Parkinson's disease | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
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 | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) DE (Completed) GB (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-008712-98 | Sponsor Protocol Number: CAFQ056A2208 | Start Date*: 2009-05-18 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: 13-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: moderate to severe levodopa induced dyskinesias in patients with Parkinson's disease | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) ES (Completed) FR (Completed) IT (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001929-20 | Sponsor Protocol Number: TEST-APO | Start Date*: 2010-05-18 | |||||||||||||||||||||
Sponsor Name:Servicio de Psiquiatría. Hospital Universitari Vall dHebron | |||||||||||||||||||||||
Full Title: EL TEST DE APOMORFINA COMO MARCADOR BIOLÓGICO DE LAS RECAÍDAS EN PACIENTES DEPENDIENTES DE SUSTANCIAS PSICOTROPAS | |||||||||||||||||||||||
Medical condition: Dependencia de alcohol Dependencia de cocaína Dependencia de heroína | |||||||||||||||||||||||
|
|||||||||||||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here

Download Options: | |
---|---|
Number of Trials to download: | |
Download Content: | |
Download Format: | |
Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. |
