- Trials with a EudraCT protocol (24)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (635)
24 result(s) found for: Amine.
Displaying page 1 of 2.
EudraCT Number: 2018-002474-52 | Sponsor Protocol Number: AM-125-CL-18-01 | Start Date*: 2019-04-01 | |||||||||||
Sponsor Name:Auris Medical AG | |||||||||||||
Full Title: Multicenter randomized controlled phase 2 trial to evaluate AM-125 in the treatment of acute peripheral vertigo following neurosurgery (TRAVERS) | |||||||||||||
Medical condition: Treatment of acute peripheral vertigo | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) CZ (Completed) PL (Completed) DE (Completed) GB (GB - no longer in EU/EEA) SK (Completed) IT (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000752-33 | Sponsor Protocol Number: SPL7013-016 | Start Date*: 2012-06-22 |
Sponsor Name:Starpharma Pty Ltd | ||
Full Title: A phase 3, double-blind, multicenter, randomized, placebo-controlled study to assess the efficacy and safety of SPL7013 Gel (VivaGel®) for the treatment of bacterial vaginosis | ||
Medical condition: Bacterial vaginosis | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Female | |
Trial protocol: DE (Completed) BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-003912-23 | Sponsor Protocol Number: ADX10059-202 | Start Date*: 2006-10-26 |
Sponsor Name:Addex Pharmaceuticals SA | ||
Full Title: A Phase IIa, double-blind, placebo-controlled, randomised, parallel-group study, to investigate the safety, tolerability and anxiolytic effect of the mGluR5 negative allosteric modulator ADX10059 i... | ||
Medical condition: Dental anxiety | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-004292-41 | Sponsor Protocol Number: BECRO/VF/FEMALE | Start Date*: 2017-02-20 | |||||||||||
Sponsor Name:Verisfield (UK) Ltd., Greek branch | |||||||||||||
Full Title: Therapeutic Equivalence (non-inferiority), Randomized, Observer-blind, two Parallel Group, Clinical Trial for Comparing the Efficacy and Tolerability of a Generic Formulation of Vaginal Ovule conta... | |||||||||||||
Medical condition: Bacterial Vaginosis | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002089-74 | Sponsor Protocol Number: Matyus-2008/1 | Start Date*: 2008-08-15 | |||||||||||||||||||||
Sponsor Name:Semmelweis University | |||||||||||||||||||||||
Full Title: The investigation of the effect of dihydralazine (Depressan) on macular edema of type 2 diabetes patients and of inhibition of semicarbazide-sensitive amine oxidase (SSAO). | |||||||||||||||||||||||
Medical condition: Macular edema in patients with type 2 diabetes. | |||||||||||||||||||||||
|
|||||||||||||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: HU (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000587-42 | Sponsor Protocol Number: RVT-101-3002 | Start Date*: 2016-08-17 | |||||||||||
Sponsor Name:Axovant Sciences Limited | |||||||||||||
Full Title: A Long-Term, Open-Label Extension Study of the Safety and Tolerability of RVT-101 in Subjects with Alzheimer’s Disease | |||||||||||||
Medical condition: Alzheimer's Disease | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Prematurely Ended) SK (Prematurely Ended) ES (Prematurely Ended) BG (Prematurely Ended) DE (Prematurely Ended) GB (Prematurely Ended) HR (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-002957-37 | Sponsor Protocol Number: RVT-101-3001 | Start Date*: 2016-04-22 | |||||||||||
Sponsor Name:Axovant Sciences Ltd. | |||||||||||||
Full Title: A Phase 3, double-blind, randomized study of RVT-101 versus placebo when added to existing stable donepezil treatment in subjects with mild to moderate Alzheimer’s disease | |||||||||||||
Medical condition: Alzheimer’s Disease | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) CZ (Completed) SK (Completed) ES (Completed) BG (Completed) HR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-001488-51 | Sponsor Protocol Number: ADX10059-201 | Start Date*: 2006-08-01 | |||||||||||
Sponsor Name:Addex Pharmaceuticals S.A. | |||||||||||||
Full Title: A DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY, TO INVESTIGATE THE EFFICACY, SAFETY AND TOLERABILITY OF THE MGLUR5 NEGATIVE ALLOSTERIC MODULATOR ADX10059 IN THE ACUTE TREATMENT OF MIGRAINE | |||||||||||||
Medical condition: Migraine with or without aura | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-015165-31 | Sponsor Protocol Number: EME-08/43/39 | Start Date*: 2010-07-16 |
Sponsor Name:Northumberland, Tyne and Wear NHS Foundation Trust | ||
Full Title: Antiglucocorticoid augmentation of antiDepressants in Depression: a double-blind, randomised, placebo-controlled, parallel-group trial | ||
Medical condition: depression | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-002393-37 | Sponsor Protocol Number: RG_13-027 | Start Date*: 2015-01-06 | |||||||||||
Sponsor Name:University of Birmingham | |||||||||||||
Full Title: A single arm, two-stage, multi-centre, phase II clinical trial investigating the safety and activity of the use of BTT1023, a human monoclonal antibody targeting vascular adhesion protein (VAP-1), ... | |||||||||||||
Medical condition: Primary Sclerosing Cholangitis (PSC) | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003356-51 | Sponsor Protocol Number: ZEL001 | Start Date*: 2015-10-15 | |||||||||||
Sponsor Name:Zelmic AB | |||||||||||||
Full Title: A single-centre, open-label, single-arm, Phase I/II study to investigate the effect of a hydrogen peroxide foam on clinical signs and symptoms and the vaginal flora in patients with bacterial vagin... | |||||||||||||
Medical condition: Bacterial vaginosis | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-000081-36 | Sponsor Protocol Number: SAT1-05-04 | Start Date*: 2007-05-02 | |||||||||||
Sponsor Name:GPC Biotech AG | |||||||||||||
Full Title: Ensayo en Fase I-II para evaluar la administración de radioterapia concomitante prequirúrgica y quimioterapia con satraplatin más capecitabina en el tratamiento del adenocarcinoma rectal localment... | |||||||||||||
Medical condition: Adenocarcinoma rectal localmente avanzado | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001970-33 | Sponsor Protocol Number: 167700-002CL | Start Date*: 2013-07-19 | |||||||||||
Sponsor Name:Proximagen Limited | |||||||||||||
Full Title: A Double-Blind, Randomised, Exploratory Study to Investigate the Safety, Efficacy and Pharmacokinetics of PRX167700 in Subjects with Knee Osteoarthritis. | |||||||||||||
Medical condition: Osteoarthritis of the knee | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004396-12 | Sponsor Protocol Number: 02 | Start Date*: 2015-02-03 | |||||||||||
Sponsor Name:Azienda Ospedaliero-Universitaria Meyer | |||||||||||||
Full Title: Efficacy of ketamine in refractory convulsive status epilepticus in children: a multicenter, randomized, controlled, open-label, no-profit, with sequential design study. | |||||||||||||
Medical condition: Refractory convulsive status epilepticus, defined as the recurrence of crisis for more than 60 minutes and / or drug-resistant I l and II line. | |||||||||||||
|
|||||||||||||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004563-37 | Sponsor Protocol Number: IPR_GARDEFLORA_15-2 | Start Date*: 2016-12-27 | |||||||||||
Sponsor Name:Laboratoires IPRAD PHARMA | |||||||||||||
Full Title: Study of the efficacy and safety of treatment with completely lyophilised cultures of Lactobacillus crispatus - IP 174178 administered intravaginally in the treatment of bacterial vaginosis. | |||||||||||||
Medical condition: Bacterial vaginosis | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: PL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000499-83 | Sponsor Protocol Number: 1386.4 | Start Date*: 2017-05-04 | |||||||||||
Sponsor Name:Boehringer Ingelheim bv | |||||||||||||
Full Title: A multi-centre, double-blind, parallel-group, randomised, placebo controlled phase II a study to investigate safety, tolerability, pharmacodynamics, and harmacokinetics of different doses of orall... | |||||||||||||
Medical condition: Non-alcoholic steatohepatitis | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) BE (Completed) DE (Completed) IE (Completed) GB (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022054-16 | Sponsor Protocol Number: X-03016-3284 | Start Date*: 2011-09-05 | |||||||||||
Sponsor Name:MEDA Pharma GmbH & Co. KG | |||||||||||||
Full Title: Long-term effects of Aldara® 5% cream and Solaraze® 3% gel in the treatment of actinic keratoses on the face or scalp with respect to the risk of progression to in-situ and invasive squamous cel... | |||||||||||||
Medical condition: This study will compare the long term effects of Aldara® and Solaraze® of the actinic keratoses on the face or scalp. Actinic keratoses (AKs) are defined as keratotic macules, papules or plaques w... | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004884-24 | Sponsor Protocol Number: X-03016-3271 | Start Date*: 2008-08-04 | |||||||||||
Sponsor Name:MEDA Pharma GmbH & Co. KG | |||||||||||||
Full Title: Long-term effects of Aldara® 5% cream and Solaraze® 3% gel in the treatment of actinic keratoses on the face or scalp (LEIDA) | |||||||||||||
Medical condition: This study will investigate the long term effects of Aldara® and Solaraze® on Actinic keratoses (AKs) on the face or scalp. AKs are defined as keratotic macules, papules or plaques with superficia... | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) AT (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000328-42 | Sponsor Protocol Number: CP-104 | Start Date*: 2007-08-03 | |||||||||||
Sponsor Name:Arrow Therapeutics Ltd | |||||||||||||
Full Title: A clinical pharmacology study to determine the pharmacokinetic , safety and tolerability profile and antiviral activity of multiple oral doses of A-831 in otherwise healthy male Hepatitis C carrie... | |||||||||||||
Medical condition: Male Hepatitis C carriers with compensated liver disease | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-017901-12 | Sponsor Protocol Number: LYO_2009-09 | Start Date*: 2010-02-26 | |||||||||||
Sponsor Name:LYOCENTRE | |||||||||||||
Full Title: Etude de l’efficacité et de la tolérance du traitement par la culture totale lyophilisée de lactobacillus casei variété rhamnosus (Lcr35 Lc) administré par voie vaginale dans la prévention de réci... | |||||||||||||
Medical condition: vaginose bactérienne récidivante | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (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 . This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
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. |
Query did not match any studies.