- Trials with a EudraCT protocol (9,517)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
9,517 result(s) found for: e.
Displaying page 131 of 476.
| EudraCT Number: 2009-016778-34 | Sponsor Protocol Number: TH09001 | Start Date*: 2010-01-27 | ||||||||||||||||||||||||||
| Sponsor Name:THERABEL LUCIEN PHARMA | ||||||||||||||||||||||||||||
| Full Title: Evaluation de la non-infériorité de l’efficacité d’Helicidine® versus Sirop à base de dextromethorphane sur la toux sèche des patients pris en charge en médecine générale. | ||||||||||||||||||||||||||||
| Medical condition: Patients volontaires présentant un épisode de toux sèche et venant consulter en médecine générale. | ||||||||||||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: FR (Ongoing) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2010-022945-52 | Sponsor Protocol Number: ADVL0516 | Start Date*: 2012-01-26 | ||||||||||||||||
| Sponsor Name:Children’s Oncology Group | ||||||||||||||||||
| Full Title: A Phase 1 Study of BMS-354825 (Dasatinib) in Children with Recurrent/Refractory Solid Tumors or Imatinib Resistant Ph+ Leukemia. | ||||||||||||||||||
| Medical condition: Refractory solid tumors Ph+ leukemia | ||||||||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: Outside EU/EEA | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2016-001875-57 | Sponsor Protocol Number: 106524 | Start Date*: 2017-03-13 | |||||||||||||||||||||
| Sponsor Name:Erasmus University Medical Center Rotterdam | |||||||||||||||||||||||
| Full Title: Desmopressin and FVIII concentrate combination treatment in non-severe hemophilia A patients undergoing minor interventions | |||||||||||||||||||||||
| Medical condition: Hemophilia A | |||||||||||||||||||||||
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| Population Age: Adolescents, Under 18, Elderly | Gender: Male | ||||||||||||||||||||||
| Trial protocol: NL (Ongoing) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2017-001770-42 | Sponsor Protocol Number: 4745 | Start Date*: 2018-10-24 | |||||||||||||||||||||
| Sponsor Name:The Royal Marsden NHS Foundation Trust | |||||||||||||||||||||||
| Full Title: A multicenter phase II non-randomised trial assessing the efficacy of Domatinostat plus avelumab in patients with previously treated advanced mismatch repair proficient oesophagogastric and colore... | |||||||||||||||||||||||
| Medical condition: Advanced gastrooesophageal and colorectal cancer | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2016-000644-34 | Sponsor Protocol Number: 108638 | Start Date*: 2016-06-09 | |||||||||||
| Sponsor Name:GlaxoSmithKline Biologicals | |||||||||||||
| Full Title: A phase III, open, randomised, multicentre study to assess the immunogenicity and safety of GlaxoSmithKline (GSK) Biologicals’ combined reduced antigen content diphtheria-tetanus toxoids and acellu... | |||||||||||||
| Medical condition: Healthy volunteers (Immunisation against diphtheria, tetanus and pertussis) | |||||||||||||
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| Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-001514-97 | Sponsor Protocol Number: 114541 | Start Date*: 2015-05-27 |
| Sponsor Name:GlaxoSmithKline Biologicals | ||
| Full Title: A Phase 3, observer blind, randomized, non-influenza vaccine comparator-controlled, multi-country and multi-centre study of the efficacy of GSK Biologicals’ quadrivalent, inactivated, split virion,... | ||
| Medical condition: Healthy volunteers (Immunization against influenza in male and female subjects 3 to 8 years of age inclusive) | ||
| Disease: | ||
| Population Age: Children, Under 18 | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA | ||
| Trial results: View results | ||
| EudraCT Number: 2005-000162-40 | Sponsor Protocol Number: IFN 001 | Start Date*: 2005-09-06 |
| Sponsor Name:Helix Product Development (Ireland) Limited | ||
| Full Title: Treatment of genital warts with Interferon alpha-2b Cream: a randomized, double blind, placebo-controlled study | ||
| Medical condition: Condylomata acuminata (genital warts) | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: SE (Completed) DE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2007-004574-11 | Sponsor Protocol Number: CS1008-A-E202 | Start Date*: 2009-05-26 | |||||||||||||||||||||
| Sponsor Name:Daiichi Sankyo Development Limited | |||||||||||||||||||||||
| Full Title: RANDOMISED, DOUBLE-BLINDED, PLACEBO- CONTROLLED PHASE 2 STUDY OF CS-1008 IN COMBINATION WITH CARBOPLATIN/PACLITAXEL IN CHEMOTHERAPY NAÏVE SUBJECTS WITH METASTATIC OR UNRESECTABLE NON-SMALL CELL LU... | |||||||||||||||||||||||
| Medical condition: Treatment of metastatic or unresectable non small cell lung cancer (NSCLC) with CS 1008 or placebo first in combination with carboplatin/paclitaxel then as monotherapy in the first line setting | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2008-000330-50 | Sponsor Protocol Number: EC07/90285 | Start Date*: 2008-10-27 | |||||||||||
| Sponsor Name:Organisation name was not entered | |||||||||||||
| Full Title: EFECTO DE SUPLEMENTACIÓN NUTRICIONAL ENRIQUECIDA CON ÁCIDOS GRASOS OMEGA-3 EN EL ESTRÉS OXIDATIVO Y METABOLISMO LIPÍDICO DE PACIENTES CON PROCESOS ONCOLÓGICOS DEL ÁREA OTORRINOLARINGOLÓGICA (ORL) ... | |||||||||||||
| Medical condition: Determinar las modificaciones inducidas por la suplementación especifica de ácidos grasos omega3 en el estrés oxidativo y estado inflamatorio en pacientes oncológicos sometidos a tratamiento radiot... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-002077-12 | Sponsor Protocol Number: MR-2008/001 | Start Date*: 2008-09-24 | |||||||||||||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA DI PERUGIA | |||||||||||||||||||||||
| Full Title: Fenoldopam end Renal failure (FENO-HSR) | |||||||||||||||||||||||
| Medical condition: Renal failure from ipoperfusion post Cardiac surgery | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2010-022762-27 | Sponsor Protocol Number: PEN1011 | Start Date*: 2010-11-09 | |||||||||||
| Sponsor Name:Klinisk Farmakologisk Afdeling, Bispebjerg | |||||||||||||
| Full Title: Studiets formål er, at undersøge hvorvidt v-penicillin og trimethoprim inducerer oxidativt stress i raske frivillige forsøgsdeltagere. En eventuel induktion vurderes ud fra målinger på 8-oxoGuo- og... | |||||||||||||
| Medical condition: Oxidative stress induced by antibiotics | |||||||||||||
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| Population Age: Adults | Gender: Male | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-021399-26 | Sponsor Protocol Number: CUERVO-07 | Start Date*: 2011-01-12 | ||||||||||||||||
| Sponsor Name:Fundación para la Formación y la Investigación de los profesionales de la Salud (FUNDESALUD) | ||||||||||||||||||
| Full Title: ENSAYO CLÍNICO CRUZADO PARA EVALUAR LA EFICACIA DEL TRATAMIENTO CON CITRATO DE FENTANILO ORAL TRANSMUCOSA DE LA DISNEA DE ESFUERZO EN PACIENTES CON CÁNCER AVANZADO | ||||||||||||||||||
| Medical condition: Disnea de esfuerzo en pacientes con cáncer avanzado | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: ES (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2011-005884-25 | Sponsor Protocol Number: 1553-B-211 | Start Date*: 2012-03-13 |
| Sponsor Name:Servicio de Endocrinologia y Nutricion. Hospital Universitari Bellvitge | ||
| Full Title: Study of the effectiveness of bariatric surgery in the treatment of type II Diabetes Mellitus in patients with grade I obesity | ||
| Medical condition: Diabetes mellitus 2 | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2013-001688-22 | Sponsor Protocol Number: 01CCRe-IV | Start Date*: 2013-08-23 | |||||||||||
| Sponsor Name:Servicio de Cirugía General y Digestiva Hospital Universitario de Bellvitge | |||||||||||||
| Full Title: Randomized multicenter trial in colorectal cancer patients with non-resectable metastasis. Impact of tumor resection versus chemotherapy alone in survival. | |||||||||||||
| Medical condition: Cancer colorectal stage IV with synchronous non-resectable metastasis. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-005068-29 | Sponsor Protocol Number: C2006-01 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:A.P. Pharma, Inc. | |||||||||||||
| Full Title: A Pivotal Phase 3 Observer-Blind, Randomized Clinical Trial of the Efficacy and Safety of APF530 Compared to Aloxi® for the Prevention of Acute-Onset and Delayed-Onset Chemotherapy-Induced Nausea a... | |||||||||||||
| Medical condition: Chemotherapy Induced Nausea and Vomiting | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: PL (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-000233-18 | Sponsor Protocol Number: AIO KRK 0205 | Start Date*: 2008-04-09 | |||||||||||
| Sponsor Name:Universität zu Köln | |||||||||||||
| Full Title: Phase I/II Studie zum Einsatz von Capecitabin und Oxaliplatin (XELOX) in Kombination mit Bevacizumab und Imatinib in der Erstlinientherapie von Patienten mit fortgeschrittenem kolorektalem Karzinom | |||||||||||||
| Medical condition: fortgeschrittenes kolorektalen Karzinom mit inoperablen Metastasen | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-007241-12 | Sponsor Protocol Number: PH-L19SIPI131-07/07 | Start Date*: 2008-10-06 | |||||||||||
| Sponsor Name:Philogen S.p.A. | |||||||||||||
| Full Title: A PHASE I/II DOSE FINDING AND EFFICACY STUDY OF THE TUMOUR TARGETING HUMAN 131I-L19SIP MONOCLONAL ANTIBODY IN PATIENTS WITH CANCER | |||||||||||||
| Medical condition: Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-005327-41 | Sponsor Protocol Number: INT0211 | Start Date*: 2012-04-05 | |||||||||||
| Sponsor Name:ISTITUTO NAZIONALE PER LA CURA TUMORI | |||||||||||||
| Full Title: Clinical trial randomized and controlled to compare the analgesic efficacy of the association zoledronic acid and 153Sm-lexidronam vs zoledronic acid in patients with skeletal metastases from hormo... | |||||||||||||
| Medical condition: Population enrolled in the study is represented by patients bearing advanced prostatic cancer with skeletal metastases and bone pain cancer-associated and treated with analgesic drugs | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-001905-42 | Sponsor Protocol Number: LDLL600.201 | Start Date*: 2014-10-23 | |||||||||||
| Sponsor Name:AOP Oprhan Pharmaceuticals AG | |||||||||||||
| Full Title: Open-label Two-arm PD and PK Study of Landiolol in Patients with Tachycardic Atrial Fibrillation or Atrial Flutter | |||||||||||||
| Medical condition: 20 Caucasian patients with tachycardic atrial fibrillation (AF) or atrial flutter (AFL) | |||||||||||||
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-001056-35 | Sponsor Protocol Number: TXA | Start Date*: 2014-11-24 | |||||||||||
| Sponsor Name:IRCCS Istituto Giannina Gaslini | |||||||||||||
| Full Title: The Effectiveness and Population Pharmacokinetics and Pharmacogenomics of a Reduced Dose of Tranexamic Acid for Craniosynostosis Surgery: A multicenter study. The TXA Study. | |||||||||||||
| Medical condition: craniosynostosis | |||||||||||||
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| Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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