- Trials with a EudraCT protocol (1,703)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
		
	   		
	   		    
                    
                   	
                   	    1,703 result(s) found for: Benign neoplasm.
                    
                
			
   			
		
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	| EudraCT Number: 2008-004893-42 | Sponsor Protocol Number: 1.0 | Start Date*: 2008-10-15 | ||||||||||||||||
| Sponsor Name:Medizinische Universität Wien, Universitätsklinik für dermatologie | ||||||||||||||||||
| Full Title: | ||||||||||||||||||
| Medical condition: Condyloma accuminata, Vulvar Intraepithelial Neoplasia | ||||||||||||||||||
| 
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| Population Age: Adults | Gender: Female | |||||||||||||||||
| Trial protocol: AT (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2012-002053-29 | Sponsor Protocol Number: 03042012 | Start Date*: 2012-08-10 | |||||||||||
| Sponsor Name:Karolinska Institutet and University Hospital | |||||||||||||
| Full Title: PET/CT-biopsi study A PET/CT biopsy sub study in patients who have given informed consent to participate in a randomized, dubbel blind, placebo controlled phase III trial with Capecitabine +/- So... | |||||||||||||
| Medical condition: Morphological verifications of metastatic lesions, PET Ribonucleic Acid (RNA)-expression study in subjects with locally advance or metastatic HER2-negative breast cancer. | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: SE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-004749-41 | Sponsor Protocol Number: NEO-ONE | Start Date*: 2011-12-13 | |||||||||||
| Sponsor Name:TweeSteden hospital | |||||||||||||
| Full Title: The effects of neoadjuvant hormonal therapy on the course of PSA and testosterone in patients with low and intermediate-risk prostate carcinoma (NEO-ONE); A randomized controlled trial | |||||||||||||
| Medical condition: Localized prostate cancer | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: NL (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2004-000329-31 | Sponsor Protocol Number: EORTC 22011- 40014 | Start Date*: 2004-09-15 | |||||||||||
| Sponsor Name:E.O.R.T.C. - EUROPEAN ORGANIZATION FOR RESEARCH AND TREATMENT OF CANCER | |||||||||||||
| Full Title: Continuous fluorouracil plus mitomycin C versus mitomycin C plus Cisplatin as chemotherapy combination in combined radiochemotherapy for locally advanced anal cancer. A phase II-III study | |||||||||||||
| Medical condition: Locally Advanced Anal Cancer | |||||||||||||
| 
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-000466-33 | Sponsor Protocol Number: PT/11/2015 | Start Date*: 2016-03-22 | |||||||||||
| Sponsor Name:Department of Pediatric oncology, Aarhus University hospital | |||||||||||||
| Full Title: Pharmacokinetics and pharmacodynamics of Piperacillin-Tazobactam (PT) in pediatric oncology patients with fever and neutropenia. | |||||||||||||
| Medical condition: Pediatric oncology patients with fever and neutropenia | |||||||||||||
| 
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| 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: 2008-006796-80 | Sponsor Protocol Number: TES10897 | Start Date*: 2009-04-23 | |||||||||||
| Sponsor Name:Sanofi-Aventis Recherche & Développement | |||||||||||||
| Full Title: The QUTIE Study: A Randomized, Double-Blind, Placebo-controlled Study Comparing Aflibercept Versus Placebo on the QTc interval in Cancer Patients treated with Docetaxel | |||||||||||||
| Medical condition: Cancer | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) BE (Completed) DK (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-005238-19 | Sponsor Protocol Number: CD-2007-01 | Start Date*: 2007-07-26 | |||||||||||
| Sponsor Name:Instituto Cientifico y Tecnologico de Navarra | |||||||||||||
| Full Title: Estudio fase II con inmunoterapia mediante células dendríticas y linfocitos infiltrantes de tumor en tumores sólidos | |||||||||||||
| Medical condition: Melanoma, renal cell carcinoma, hepatocarcinoma | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-001359-60 | Sponsor Protocol Number: Vasobrain01 | Start Date*: 2015-06-16 | |||||||||||
| Sponsor Name:Aarhus University Hospital | |||||||||||||
| Full Title: Influence of vasopressors on brain oxygenation and microcirculation in anesthetized patients with cerebral tumors | |||||||||||||
| Medical condition: Brain oxygenation and microcirculation under administration of Efedrin and Metaoxedrin in patients with cerebral tumor. | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-022270-14 | Sponsor Protocol Number: 20101116 | Start Date*: 2011-02-11 | |||||||||||
| Sponsor Name:Amgen Inc | |||||||||||||
| Full Title: Estudio abierto de extensión de fase 2 con conatumumab . A Phase 2 Open Label Extension Study of Conatumumab. | |||||||||||||
| Medical condition: diferentes tumores sólidos, incluyendo, entre otros, cáncer colorrectal (CCR), cáncer de pulmón de células no pequeñas (CPCNP), sarcoma de tejidos blandos (STB), linfoma no Hodgkin (LNH), cáncer de... | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-006449-14 | Sponsor Protocol Number: CHUBX2008/31 | Start Date*: 2009-02-13 | |||||||||||
| Sponsor Name:CHU de Bordeaux | |||||||||||||
| Full Title: Evaluation méthodologique de la tomographie par émission de positons couplée au scanner (TEP-TDM) au Fluoromisonidazole marqué au fluor 18 ([18F]-FMISO) dans l’évaluation de la réponse au traitemen... | |||||||||||||
| Medical condition: Glioblastome | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-006411-20 | Sponsor Protocol Number: CHUBX 2008/20 | Start Date*: 2009-02-13 | |||||||||||
| Sponsor Name:CHU de Bordeaux | |||||||||||||
| Full Title: EVALUATION PRONOSTIQUE DE LA TOMOGRAPHIE PAR EMISSION DE POSITONS COUPLEE AU SCANNER (TEP-TDM) AU FLUOROMISONIDAZOLE MARQUE AU FLUOR 18 (18F-FMISO) DANS LES CANCERS EPIDERMOIDES DES VOIES AERODIGES... | |||||||||||||
| Medical condition: CANCERS EPIDERMOIDES DES VOIES AERODIGESTIVES SUPERIEURES | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-005042-42 | Sponsor Protocol Number: CURF18PSM0001 | Start Date*: 2021-06-27 | |||||||||||||||||||||||||||||||
| Sponsor Name:CURIUM Austria GmbH | |||||||||||||||||||||||||||||||||
| Full Title: Prospective study of added value of florastamin (18F) PET/CT in localisation of clinically significant prostate cancer in patients with PI-RADS≤3 report of multi-parametric MRI, elevated serum PSA ... | |||||||||||||||||||||||||||||||||
| Medical condition: Prostate cancer suspected clinically and on the basis of elevated serum Prostate Specific Antigen (PSA) levels and PSA density and with result of multiparametric Magnetic Resonance Imaging (mpMRI) ... | |||||||||||||||||||||||||||||||||
| 
 | |||||||||||||||||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male | ||||||||||||||||||||||||||||||||
| Trial protocol: AT (Trial now transitioned) | |||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2007-007059-14 | Sponsor Protocol Number: GlutOxa2007 | Start Date*: 2007-11-15 | |||||||||||
| Sponsor Name:AZIENDA DI RILIEVO NAZIONALE E DI ALTA SPECIALIZZAZIONE OSPEDALE CIVICO E BENFRATELLI, G.DI CRISTINA E M.ASCOLI | |||||||||||||
| Full Title: Role of the Glutatione reduced in the prevention of neuro-toxicity from Oxaliplatino. | |||||||||||||
| Medical condition: Patients with neoplasia malignant. | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2004-001456-36 | Sponsor Protocol Number: EGF100151 | Start Date*: 2004-09-06 | |||||||||||
| Sponsor Name:GLAXO SMITHKLINE | |||||||||||||
| Full Title: A phase III, randomized, open-label, multicenter study comparing GW572016 and Capecitabile (Xeloda) versus Capecitabile in women with refractory advanced or metastatic breast cancer. | |||||||||||||
| Medical condition: Solid tumor treatment | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-000045-12 | Sponsor Protocol Number: PEVERENAL | Start Date*: 2013-07-06 | |||||||||||
| Sponsor Name:Centre François Baclesse | |||||||||||||
| Full Title: | |||||||||||||
| Medical condition: | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-005967-33 | Sponsor Protocol Number: lung1 | Start Date*: 2009-02-20 | ||||||||||||||||
| Sponsor Name:AZIENDA OSPEDALIERO UNIVERSITARIA OSPEDALI RIUNITI UMBERTO I - G.M.LANCISI - G.SALESI | ||||||||||||||||||
| Full Title: randomized phase II trial of two different sequences in first line chemotherapy of advanced non small cell lung cancer | ||||||||||||||||||
| Medical condition: non small cell lung cancer | ||||||||||||||||||
| 
 | ||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2014-005486-75 | Sponsor Protocol Number: I3Y-MC-JPBY | Start Date*: 2015-07-24 | |||||||||||
| Sponsor Name:Lilly S.A. | |||||||||||||
| Full Title: neoMONARCH: A Phase 2 Neoadjuvant Trial Comparing the Biological Effects of 2 Weeks of Abemaciclib (LY2835219) in Combination with Anastrozole to those of Abemaciclib Monotherapy and Anastrozole Mo... | |||||||||||||
| Medical condition: Postmenopausal Women with Hormone Receptor Postive, HER2 Negative Breast Cancer | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: ES (Completed) AT (Completed) DE (Completed) NL (Completed) BE (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-020402-15 | Sponsor Protocol Number: 1651/YE | Start Date*: 2010-09-03 | |||||||||||
| Sponsor Name:Develco Pharma Schweiz AG | |||||||||||||
| Full Title: Randomised, double-blind, cross-over Phase III study to investigate the efficacy and safety of oxycodone after once daily administration of Oxycodone HCl XL tablets in comparison to twice daily adm... | |||||||||||||
| Medical condition: Chronic cancer pain | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) HU (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-000563-25 | Sponsor Protocol Number: 2011/119/HP | Start Date*: 2012-07-27 | |||||||||||
| Sponsor Name:CHU-Hôpitaux de Rouen | |||||||||||||
| Full Title: Randomized phase III study of gemcitabine and cisplatin (GC) versus high dose intensity methotrexate, vinblastine, doxorubicin and cisplatin (HD-MVAC) in the perioperative setting for patients with... | |||||||||||||
| Medical condition: locally advanced transitional cell cancer of the bladder | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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