- Trials with a EudraCT protocol (44,395)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
44,395 result(s) found.
Displaying page 1,071 of 2,220.
| EudraCT Number: 2017-004686-28 | Sponsor Protocol Number: 14143JK-AS | Start Date*: 2018-07-16 |
| Sponsor Name:Belfast Health and Social Care Trust (BHSCT) | ||
| Full Title: A randomised, double-blind, placebo-controlled trial to evaluate the effect of Epstein-Barr virus suppression in chronic obstructive pulmonary disease (EViSCO trial). | ||
| Medical condition: Epstein-Barr virus infection in patients with chronic obstructive pulmonary disease. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-017101-11 | Sponsor Protocol Number: Tem/Erlo in NSCLC-Pilotstudy | Start Date*: 2010-09-08 |
| Sponsor Name:MUW, Klinik für Innere Medizin I, Onkologie | ||
| Full Title: A Pilot Study of Erlotinib and Temsirolimus in Patients with Advanced Non-small Cell Lung Cancer After Failure of at Least 1 Prior Platinum-based Treatment | ||
| Medical condition: NSCLC | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2010-019423-61 | Sponsor Protocol Number: GENRAS | Start Date*: 2010-10-28 |
| Sponsor Name:Medizinische Universität Wien,Univ.Klinik f.Psychiatrie und Psychotherapie | ||
| Full Title: GENRAS (GENetics of Response to Agomelatine vs. EScitalopram) | ||
| Medical condition: depressive disorder | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2013-001656-35 | Sponsor Protocol Number: 109MS408 | Start Date*: 2014-04-07 | ||||||||||||||||
| Sponsor Name:Biogen Idec Research Limited | ||||||||||||||||||
| Full Title: A Multicenter, Open-Label Study Evaluating the Effectiveness of Oral Tecfidera™ (Dimethyl Fumarate) on MS Disease Activity and Patient-Reported Outcomes in Subjects with Relapsing-Remitting Multipl... | ||||||||||||||||||
| Medical condition: Relapsing-Remitting Multiple Sclerosis | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: AT (Completed) HU (Completed) BE (Completed) PT (Completed) IT (Completed) CZ (Completed) SK (Completed) ES (Completed) SI (Completed) FR (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2014-001463-12 | Sponsor Protocol Number: P130936 | Start Date*: 2015-03-13 | |||||||||||
| Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
| 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: 2011-002408-34 | Sponsor Protocol Number: Nosponsor | Start Date*: 2011-10-05 | |||||||||||
| Sponsor Name:Matti Ristikankare | |||||||||||||
| Full Title: | |||||||||||||
| Medical condition: | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-003284-38 | Sponsor Protocol Number: EVG001SAH | Start Date*: 2016-02-15 | |||||||||||
| Sponsor Name:Evgen Pharma plc | |||||||||||||
| Full Title: SFX-01 AFTER SUBARACHNOID HAEMORRHAGE | |||||||||||||
| Medical condition: Subarachnoid Haemorrhage | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-005774-37 | Sponsor Protocol Number: GETNE-2016-01 | Start Date*: 2016-04-29 | |||||||||||
| Sponsor Name:Grupo Español de Tumores Neuroendocrinos. SECRETARÍA TÉCNICA GETNE (GETNE) | |||||||||||||
| Full Title: Phase II study to evaluate efficacy of rechallenge with Sunitinib in Patients with Metastatic Pancreatic Neuroendocrine Tumor (pNETs) well differentiated G1/2 advanced or metastatic who previously ... | |||||||||||||
| Medical condition: Metastatic Pancreatic Neuroendocrine Tumor (pNETs) well differentiated G1/2 advanced or metastatic | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-003378-28 | Sponsor Protocol Number: 2013071339 | Start Date*: 2014-04-09 | |||||||||||
| Sponsor Name:Department of Medicine, Køge University Hospital [...] | |||||||||||||
| Full Title: THE ROLE OF PHAGES IN MICROBIAL GUT ECOLOGY A STUDY OF INTERACTIONS BETWEEN ANTIBIOTICS AND THE GUT MICROBIOTA IN HEALTHY VOLUNTEERS A PARALLEL, SINGLE-BLIND, RANDOMIZED, CONTROLLED STUDY | |||||||||||||
| Medical condition: Resistance to anitbiotics | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-000383-28 | Sponsor Protocol Number: CLI/016P | Start Date*: 2015-01-12 |
| Sponsor Name:Dexcel Pharma Technologies Ltd. | ||
| Full Title: The Efficacy and Safety of Chlorhexidine Gluconate Chip (PerioChip®) in Therapy of Peri-implantitis | ||
| Medical condition: Peri-implantitis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-003539-56 | Sponsor Protocol Number: 1.01 | Start Date*: 2006-11-10 |
| Sponsor Name:Medical University of Vienna, Department of Internal Medicine IV | ||
| Full Title: Simvastatin in patients with septic shock | ||
| Medical condition: Septic shock | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2016-003852-60 | Sponsor Protocol Number: NSR-RPGR-01 | Start Date*: 2017-01-09 | |||||||||||
| Sponsor Name:NightstaRx Limited | |||||||||||||
| Full Title: A Dose Escalation (Phase 1), and Dose Expansion (Phase 2/3) Clinical Trial of Retinal Gene Therapy for X-linked Retinitis Pigmentosa Using an Adeno-Associated Viral Vector (AAV8) Encoding Retinitis... | |||||||||||||
| Medical condition: X-Linked retinitis pigmentosa (XLRP) | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-019236-12 | Sponsor Protocol Number: GEMCAD-1002 | Start Date*: 2010-10-13 | ||||||||||||||||
| Sponsor Name:Grupo Español Multidisciplinar en Cáncer Digestivo (GEMCAD) | ||||||||||||||||||
| Full Title: Ensayo clínico fase II de un solo brazo, multicéntrico y prospectivo para la validación de biomarcadores en pacientes con cáncer colorrectal avanzado y/o metastásico con gen KRAS no mutado tratados... | ||||||||||||||||||
| Medical condition: Cancer colorrectal avanzado y/o metastásico | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: ES (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2012-004707-12 | Sponsor Protocol Number: CRAD001C2X01B | Start Date*: 2013-05-16 |
| Sponsor Name:Novartis Pharma Services AG | ||
| Full Title: An open-label, multi-center everolimus roll-over protocol for patients who have completed a previous Novartis-sponsored everolimus study and are judged by the investigator to benefit from continued... | ||
| Medical condition: Disease corresponding to the Novartis-sponsored study the patient will be transitioning from | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: CZ (Completed) NL (Prematurely Ended) IT (Completed) ES (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2004-002834-20 | Sponsor Protocol Number: HCC-Rap-001 | Start Date*: 2008-01-23 |
| Sponsor Name:Universitätsklinik für Innere Medizin IV, Klinische Abteilung Gastroenterologie und Hepatologie | ||
| Full Title: Behandlung des fortgeschrittenen hepatozellulären Karzinoms mit dem mTOR-Inhibitor Rapamycin (HCC-Rap-001) Treatment of advanced hepatocellular carcinoma with the mTOR-inhibitor rapamycin (HCC-Ra... | ||
| Medical condition: Advanced hepatocellular carcinoma (HCC) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-005184-29 | Sponsor Protocol Number: P305-R-EG04 | Start Date*: 2006-02-21 |
| Sponsor Name:GABA GmbH | ||
| Full Title: Prevention of incipient carious lesions (white spot lesions) in patients with fixed orthodontic appliances following the application of elmex® gelée | ||
| Medical condition: incipient carious lesions (white spot lesions) | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2014-004509-34 | Sponsor Protocol Number: CUDC-907-201 | Start Date*: 2016-10-13 | ||||||||||||||||
| Sponsor Name:Curis, Inc. | ||||||||||||||||||
| Full Title: Open-Label, Phase 2 Study to Evaluate the Efficacy and Safety of CUDC-907 in Patients With Relapsed/Refractory Diffuse Large B-Cell Lymphoma, Including Patients With MYC Alterations | ||||||||||||||||||
| Medical condition: Patients With Relapsed/Refractory Diffuse Large B-Cell Lymphoma including patients with MYC alterations | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) NL (Completed) ES (Completed) HU (Completed) FR (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2013-003352-20 | Sponsor Protocol Number: 469055 | Start Date*: 2016-07-18 | |||||||||||
| Sponsor Name:University Medical Center of Johannes -Gutenberg University Mainz | |||||||||||||
| Full Title: Correlation of functional and structural outcomes with serum antibody profiles in patients with neovascular age-related macular degeneration treated with ranibizumab and healthy subjects: a prospec... | |||||||||||||
| Medical condition: Neovascular age-related macular degeneration (AMD) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-000833-40 | Sponsor Protocol Number: CCR4502 | Start Date*: 2016-10-07 |
| Sponsor Name:The Institute of Cancer Research | ||
| Full Title: Phase I ’run in’ study followed by randomised phase II trial testing intra-tumoural hydrogen peroxide as a radiation sensitizer in patients with locally advanced/recurrent breast cancer in terms of... | ||
| Medical condition: Women with locally advanced/recurrent breast cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2018-003257-16 | Sponsor Protocol Number: CitraFleet_H-2018 | Start Date*: 2018-11-07 | |||||||||||
| Sponsor Name:Goodwill Pharma Kft. | |||||||||||||
| Full Title: Efficacy, Safety and Tolerability of CitraFleet, a New Bowel Cleansing Agent – a Prospective, Single-Center, Single-Group Phase IV Study | |||||||||||||
| Medical condition: Colonoscopy bowel preparation | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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