- Trials with a EudraCT protocol (44,394)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (18,700)
44,394 result(s) found.
Displaying page 887 of 2,220.
| EudraCT Number: 2008-007319-33 | Sponsor Protocol Number: OP08/8679 | Start Date*: 2009-02-19 |
| Sponsor Name:Leeds Teaching Hospitals NHS Trust | ||
| Full Title: Do genes predict response to treatment in age-related macular degeneration? | ||
| Medical condition: Choroidal neovascularisation secondary to age-related macular degeneration (ARMD) | ||
| Disease: | ||
| Population Age: Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2010-022772-31 | Sponsor Protocol Number: 20100812v2 | Start Date*: 2011-02-09 | |||||||||||
| Sponsor Name:Medizinische Universität Wien, Universitätsklinik für Psychiatrie und Psychotherapie | |||||||||||||
| Full Title: Brain Network Dysfunction as a Model for Schizophrenia: Connectivity Alterations using Ketamine and pharmacological Magnetic Resonance Imaging | |||||||||||||
| Medical condition: Quantify changes of resting-state functional connectivity in response to Esketamine in healthy volunteers. | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-021793-12 | Sponsor Protocol Number: AC-052-374 | Start Date*: 2011-04-04 | |||||||||||||||||||||
| Sponsor Name:Actelion Pharmaceuticals Ltd. | |||||||||||||||||||||||
| Full Title: A prospective, multicenter, open-label extension of FUTURE 3 to assess the safety, tolerability and efficacy of the pediatric formulation of bosentan two versus three times a day in children with p... | |||||||||||||||||||||||
| Medical condition: Pulmonary arterial hypertension (PAH) in children | |||||||||||||||||||||||
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| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: DE (Completed) HU (Completed) CZ (Completed) FR (Ongoing) NL (Completed) ES (Completed) IT (Completed) PL (Completed) Outside EU/EEA | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2010-019340-40 | Sponsor Protocol Number: MOZ15609-DFI12860 | Start Date*: 2010-08-23 |
| Sponsor Name:Genzyme Europe B.V. | ||
| Full Title: A Phase 1/2 Combined Dose Ranging and Randomised, Open-label, Comparative Study of the Efficacy and Safety of Plerixafor in Addition to Standard Regimens for Mobilisation of Haematopoietic Stem Cel... | ||
| Medical condition: Paediatric cancer patients (aged 1 to <18 years) with Ewing’s sarcoma/soft tissue sarcoma, lymphoma, neuroblastoma and all other malignancies (excluding leukaemia) who are planned to undergo high d... | ||
| Disease: | ||
| Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: GB (Completed) DE (Completed) IT (Completed) ES (Completed) BE (Completed) HU (Completed) CZ (Completed) NL (Completed) DK (Completed) PL (Completed) Outside EU/EEA | ||
| Trial results: View results | ||
| EudraCT Number: 2010-021870-12 | Sponsor Protocol Number: 10TASQ10 | Start Date*: 2011-02-15 | ||||||||||||||||
| Sponsor Name:Active Biotech AB | ||||||||||||||||||
| Full Title: A Phase 3 Randomized, Double-Blind, Placebo-Controlled Study of Tasquinimod in Men with Metastatic Castrate Resistant Prostate Cancer | ||||||||||||||||||
| Medical condition: Metastatic Castrate-Resistant Prostate Cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
| Trial protocol: SE (Completed) GB (Completed) BE (Completed) DE (Completed) LV (Completed) NL (Completed) CZ (Completed) ES (Completed) LT (Completed) IT (Completed) SK (Completed) GR (Completed) EE (Prematurely Ended) BG (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2010-021901-19 | Sponsor Protocol Number: PHANOS | Start Date*: 2011-05-05 | |||||||||||
| Sponsor Name:Med Uni Graz, Univ. Klinik für Anästhesiologie und Intensivmedizin | |||||||||||||
| Full Title: Reduzierter Opioidverbrauch durch Physostigmin als Dauertropf zur postoperativen PCA – PHANOS (PHysostigmine-enhANced Opioid analgeSia). prospektive, doppelblinde, randomisierte, placebokontrollie... | |||||||||||||
| Medical condition: Die Hypothese dieser prospektiven, doppelblinden, randomisierten, placebokontrollierten Studie ist, dass die kontinuierliche i.v. Gabe von Physostigmin während der ersten 24 h postoperativ zu einem... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-023473-18 | Sponsor Protocol Number: FTG_VuA_01 | Start Date*: 2011-04-14 |
| Sponsor Name:Inn-Salzach-Klinikum gGmbH | ||
| Full Title: Verkehrssicherheit unter Agomelatin | ||
| Medical condition: Diagnosis of depression; ICD-10: F32.x, F33.x | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-022202-41 | Sponsor Protocol Number: MRVstudy-10 | Start Date*: 2011-01-27 | |||||||||||
| Sponsor Name:Daniel Podzamczer | |||||||||||||
| Full Title: ESTUDIO PILOTO DEL CAMBIO EN LA ACTIVIDAD ANTIRRETROVIRAL EN SISTEMA NERVIOSO CENTRAL TRAS LA SUSTITUCIÓN DE TDF/FTC/EFV POR ABC/3TC/MVC | |||||||||||||
| Medical condition: Virus de imunodeficiencia humana-1 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-021928-96 | Sponsor Protocol Number: ISD-LAM-2010-01 | Start Date*: 2011-04-01 | |||||||||||
| Sponsor Name:ISDIN S.A. | |||||||||||||
| Full Title: Ensayo clínico multicéntrico, doble ciego, para evaluar la eficacia y seguridad de lambdalina vs placebo como anestésico en fotodepilación con láser | |||||||||||||
| Medical condition: Anestesia en Fotodepilación | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-024096-87 | Sponsor Protocol Number: Ileus_gastro | Start Date*: 2011-07-01 | |||||||||||
| Sponsor Name:Sebastiano Biondo Aglio | |||||||||||||
| Full Title: ESTUDIO CLÍNICO PROSPECTIVO ALEATORIZADO DOBLE CIEGO SOBRE LA UTILIDAD TERAPÉUTICA DEL GASTROGRAFÍN EN ÍLEO PARALÍTICO EN EL POSTOPERATORIO DE CIRUGÍA COLORRECTAL | |||||||||||||
| Medical condition: Ileo paralítico postoperatorio | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-022460-12 | Sponsor Protocol Number: MVH-03 | Start Date*: 2011-03-23 | ||||||||||||||||||||||||||
| Sponsor Name:Herlev Hospital | ||||||||||||||||||||||||||||
| Full Title: The effect of melatonin on depression, anxiety, cogntive function and sleep disturbances in breast cancer patients | ||||||||||||||||||||||||||||
| Medical condition: Depression Anxiety Postoperative cognitive dysfunction Sleep disturbances | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||
| Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2010-023242-69 | Sponsor Protocol Number: GENA-11 | Start Date*: 2011-05-31 | |||||||||||
| Sponsor Name:Octapharma AG | |||||||||||||
| Full Title: Clinical Study to Investigate the Long-Term Efficacy, Safety, and Immunogenicity of human-cl rhFVIII in Previously Treated Patients with Severe Haemophilia A – Extension Study to GENA-01 | |||||||||||||
| Medical condition: Severe haemophilia A (FVIII:C <1%) | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Male | ||||||||||||
| Trial protocol: DE (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-021143-41 | Sponsor Protocol Number: 31-10-270 | Start Date*: 2010-12-22 | |||||||||||
| Sponsor Name:Otsuka Pharmaceutical Development and Commercialization, Inc. | |||||||||||||
| Full Title: An Open-Label, Multicenter, Rollover, Long-term Study of Aripiprazole Intramuscular Depot in Patients with Schizophrenia | |||||||||||||
| Medical condition: Schizophrenia | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Completed) BG (Completed) SK (Completed) HU (Completed) EE (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-023268-42 | Sponsor Protocol Number: NICTDP2012 | Start Date*: 2011-03-25 |
| Sponsor Name:McNeil AB | ||
| Full Title: NICOTINE PHARMACODYNAMICS WITH A NEW ORAL NICOTINE REPLACEMENT PRODUCT AND NICOTINE GUM 4 MG. A STUDY IN HEALTHY SMOKERS. | ||
| Medical condition: Tobacco Dependence | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2010-024515-13 | Sponsor Protocol Number: VU-007 | Start Date*: 2011-03-22 | |||||||||||
| Sponsor Name:VU University Medical Center | |||||||||||||
| Full Title: Phase 1-2 study of everolimus and low-dose oral cyclophosphamide in patients with metastatic renal cell cancer. | |||||||||||||
| Medical condition: Metastatic renal cell cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-012258-19 | Sponsor Protocol Number: F506-CL-0403 | Start Date*: 2011-03-09 | |||||||||||||||||||||
| Sponsor Name:Astellas Pharma Europe Ltd. | |||||||||||||||||||||||
| Full Title: A Multicentre, Open-label, Pharmacokinetic Study of Modigraf® (Tacrolimus granules) in de novo Paediatric Allograft Recipients.Estudio Abierto, Multicéntrico, Farmacocinético de Modigraf® (Tacróli... | |||||||||||||||||||||||
| Medical condition: De novo allograft transplantation (liver, heart, kidney) in paediatric patients. Pacientes pediátricos que reciben un trasplante de aloinjerto de novo ( hígado, corazón y riñón) | |||||||||||||||||||||||
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| Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: ES (Completed) GB (Completed) DE (Completed) BE (Completed) FR (Ongoing) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2010-022364-12 | Sponsor Protocol Number: BAY86-5321/91745 | Start Date*: 2011-03-18 | |||||||||||
| Sponsor Name:Bayer HealthCare AG | |||||||||||||
| Full Title: A randomized, double masked, active controlled, phase III study of the efficacy and safety of repeated doses of intravitreal VEGF Trap-Eye in subjects with diabetic macular edema | |||||||||||||
| Medical condition: Diabetic macular edema with central involvement | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) AT (Completed) CZ (Completed) ES (Completed) DK (Completed) IT (Completed) HU (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-019634-26 | Sponsor Protocol Number: MPEX-209 | Start Date*: 2011-05-24 | ||||||||||||||||
| Sponsor Name:Mpex Pharmaceuticals, Inc. | ||||||||||||||||||
| Full Title: A Phase 3, Open-Label, Randomized Trial to Evaluate the Safety and Efficacy of MP-376 Inhalation Solution (Aeroquin™) versus Tobramycin Inhalation Solution (TIS) in Stable Cystic Fibrosis Patients | ||||||||||||||||||
| Medical condition: Pseudomonas aeruginosa infection in patients suffering from stable Cystic Fibrosis | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) GB (Completed) FR (Ongoing) IE (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2010-023017-65 | Sponsor Protocol Number: B1871019 | Start Date*: 2011-03-17 | |||||||||||
| Sponsor Name:Pfizer Inc., 235 East 42nd Street, New York, NY 10017 | |||||||||||||
| Full Title: A PHASE 2, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY OF THE SAFETY, CLINICAL ACTIVITY AND PHARMACOKINETICS OF BOSUTINIB (PF-05208763) VERSUS PLACEBO IN SUBJECTS WITH AUTOSOMAL... | |||||||||||||
| Medical condition: Autosomal Dominant Polycystic Kidney Disease (ADPKD) | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) ES (Completed) CZ (Completed) HU (Completed) GB (Completed) PL (Completed) SK (Completed) LT (Completed) IT (Completed) BG (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-023482-21 | Sponsor Protocol Number: 01/10/CPT/TP3 | Start Date*: 2011-04-11 | |||||||||||
| Sponsor Name:PLIVA HRVATSKA d.o.o. | |||||||||||||
| Full Title: A Multicentre, Randomised, Double-Blind, Parallel-Group Study of the Efficacy and Safety of a PLIVA Ointment (Calcipotriol + Betamethasone 50 µg/g + 0.5 mg/g ointment) versus Vehicle and Dovobet® i... | |||||||||||||
| Medical condition: mild to severe plaque psoriasis | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) SK (Completed) DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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