- Trials with a EudraCT protocol (511)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
		
	   		
	   		    
                    
                   	
                   	    511 result(s) found for: Translational research.
                    
                
			
   			
		
		Displaying page 1 of 26.
	
	
	| EudraCT Number: 2010-018837-23 | Sponsor Protocol Number: SPON-804-10 | Start Date*: 2010-12-06 | 
| Sponsor Name:Cardiff University | ||
| Full Title: A randomised Phase II study of carboplatin with or without the addition of the ETAR inhibitor ZD4054 as treatment for patients with metastatic breast cancer. | ||
| Medical condition: Metastatic Breast Cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-012151-23 | Sponsor Protocol Number: SPON 671-09 | Start Date*: 2009-11-11 | 
| Sponsor Name:Cardiff University | ||
| Full Title: A randomised phase II study of Irinotecan, 5-Fluorouracil and Folinic Acid (FOLFIRI) with or without the addition of an endothelin receptor antagonist in patients with metastatic colorectal cancer ... | ||
| Medical condition: Metastatic Colorectal Cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2008-000746-32 | Sponsor Protocol Number: 5-HT_CFM | Start Date*: 2008-04-23 | 
| Sponsor Name:Karolinska Institutet | ||
| Full Title: Validation of experimental pain models as translational for craniofacial myalgia with respect to the influence of 5-HT, glutamate, cortisol and estradiol level | ||
| Medical condition: Patients with craniomandibular myalgia (CM), i.e. with pain in the masster muscle and a diagnosis of myofascial pain according to the RDC/TMD criteria, and healthy subjects of both sexes, over 18 y... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2022-002134-14 | Sponsor Protocol Number: 1.0 | Start Date*: 2022-09-02 | 
| Sponsor Name:Catharina Hospital Eindhoven | ||
| Full Title: Intraperitoneal irinotecan with concomitant FOLFOX and bevacizumab for patients with unresectable colorectal peritoneal metastases – a phase II study | ||
| Medical condition: Patients with peritoneal carcinomatosis of colorectal origin | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-003104-12 | Sponsor Protocol Number: M19VLC | Start Date*: 2020-01-14 | |||||||||||
| Sponsor Name:NKI-AVL | |||||||||||||
| Full Title: Treatment of locally advanced VULvar CArcinoma in a Neoadjuvant setting with Carboplatin and Paclitaxel chemotherapy | |||||||||||||
| Medical condition: vulvar carcinoma | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: NL (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-001992-30 | Sponsor Protocol Number: | Start Date*: 2015-04-20 | |||||||||||
| Sponsor Name:University of Leicester | |||||||||||||
| Full Title: A randomised controlled phase II trial of oral vinorelbine as second line therapy for patients with malignant pleural mesothelioma | |||||||||||||
| Medical condition: Histologically confirmed malignant pleural mesothelioma | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-002295-18 | Sponsor Protocol Number: ML 19033 | Start Date*: 2007-01-24 | 
| Sponsor Name:University Hospital, Dept of Oncology, clinical trial unit | ||
| Full Title: ACT: Avastin and Chemotherapy followed by Avastin alone or in combination with Tarceva for the treatment of metastatic colorectal cancer | ||
| Medical condition: Patients with previously untreated metastatic colorectal carcinoma | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DK (Completed) SE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-005050-35 | Sponsor Protocol Number: 30102012 | Start Date*: 2014-12-01 | ||||||||||||||||
| Sponsor Name:University Medical Center Groningen | ||||||||||||||||||
| Full Title: Phase Ib/II study of metformin in combination with carboplatin/paclitaxel chemotherapy in patients with advanced ovarian cancer | ||||||||||||||||||
| Medical condition: advanced ovarian cancer | ||||||||||||||||||
| 
 | ||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
| Trial protocol: NL (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2010-022010-32 | Sponsor Protocol Number: PR201005 | Start Date*: 2011-08-15 | 
| Sponsor Name:Barts and The London NHS Trust | ||
| Full Title: A phase II single arm, multi-centre trial of triamcinolone with a GnRH analog for castration resistant prostate cancer | ||
| Medical condition: Castration Resistent Prostate cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2020-002821-28 | Sponsor Protocol Number: ET20-128 | Start Date*: 2020-12-24 | 
| Sponsor Name:Centre Léon Bérard | ||
| Full Title: RAR-Immune: A randomised, comparative, prospective, multicentre study of the efficacy of nivolumab + ipilimumab versus pazopanib alone in patients with metastatic or unresectable advanced sarcoma o... | ||
| Medical condition: Metastatic or unresectable advanced rare sarcomas | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2004-002371-16 | Sponsor Protocol Number: D6997C00002 (9238IL/0064) | Start Date*: 2004-11-18 | 
| Sponsor Name:AstraZeneca AB | ||
| Full Title: A Randomised, Double-Blind, Parallel-group, Multicentre, Phase III Study Comparing the Efficacy and Tolerability of Fulvestrant (FASLODEX™) 500 mg with Fulvestrant (FASLODEX™) 250 mg in Postmenopau... | ||
| Medical condition: Postmenopausal women with advanced breast cancer, progressing or relapsing after previous endocrine therapy | ||
| Disease: | ||
| Population Age: Elderly | Gender: Female | |
| Trial protocol: SK (Completed) CZ (Completed) HU (Completed) ES (Completed) IT (Completed) MT (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2011-005820-17 | Sponsor Protocol Number: 90111-24111 | Start Date*: 2012-06-07 | |||||||||||
| Sponsor Name:European Organisation for Research and Treatment of Cancer | |||||||||||||
| Full Title: Neoadjuvant BIBW 2992 followed by surgery in squamous cell carcinoma of the head and neck: an EORTC NOCI-HNCG window study. | |||||||||||||
| Medical condition: Squamous cell carcinoma of the head and neck (SCCHN) | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: | ||||||||||||
| Trial protocol: BE (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-004644-28 | Sponsor Protocol Number: 13-129 | Start Date*: Information not available in EudraCT | 
| Sponsor Name:RWTH Aachen University, represented by the Rector, himself, represented by the Dean of the Medical Faculty | ||
| Full Title: Administration of Rifaximin to improve Liver Regeneration and Outcome following Major Liver Resection | ||
| Medical condition: Patients undergoing major liver resection will be included into the study | ||
| Disease: | ||
| Population Age: Elderly | Gender: Male, Female | |
| Trial protocol: DE (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-011884-35 | Sponsor Protocol Number: SAKK 77/08 and SASL 29 | Start Date*: 2009-12-19 | 
| Sponsor Name:Swiss Group for Clinical Cancer Research | ||
| Full Title: Sorafenib alone or in combination with everolimus in patients with unresectable hepatocellular carcinoma. A randomized multicenter phase II trial. | ||
| Medical condition: Patients with unresectable hepatocellular carcinoma. | ||
| Disease: | ||
| Population Age: | Gender: Male, Female | |
| Trial protocol: HU (Completed) AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2010-018850-11 | Sponsor Protocol Number: MHH_CCA_AG54 | Start Date*: 2011-04-15 | ||||||||||||||||
| Sponsor Name:Medizinische Hochschule Hannover (MHH) | ||||||||||||||||||
| Full Title: Panitumumab in combination with cisplatin/gemcitabine chemotherapy in patients with cholangiocarcinomas - a randomized clinical phase II study - PiCCA Study | ||||||||||||||||||
| Medical condition: cholangiocarcinoma / gall bladder carcinoma | ||||||||||||||||||
| 
 | ||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
| Trial protocol: DE (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2013-002466-39 | Sponsor Protocol Number: CFTSp032 | Start Date*: 2014-01-24 | |||||||||||
| Sponsor Name:The Christie NHS Foundation Trust | |||||||||||||
| Full Title: A randomised placebo-controlled trial of synchronous NIMorazole versus RADiotherapy alone in patients with locally advanced head and neck squamous cell carcinoma not suitable for synchronous chemot... | |||||||||||||
| Medical condition: Locally advanced head and neck squamous cell carcinoma (HNSCC) | |||||||||||||
| 
 | |||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-004420-39 | Sponsor Protocol Number: 05-10 | Start Date*: 2006-05-18 | 
| Sponsor Name:All-Ireland Co-operative Oncology Research Group (ICORG) | ||
| Full Title: An Open Label Phase II Multicentre Clinical Trial of Single Agent VELCADE (Bortezomib) in Patients with Malignant Pleural Mesothelioma | ||
| Medical condition: Malignant Pleural Mesothelioma (in first line, and second line treatment settings) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: IE (Prematurely Ended) GB (Completed) BE (Completed) NL (Ongoing) | ||
| Trial results: View results | ||
| EudraCT Number: 2015-001361-27 | Sponsor Protocol Number: ICR-CTSU/2015/10054 | Start Date*: 2016-09-21 | |||||||||||
| Sponsor Name:The Institute of Cancer Research | |||||||||||||
| Full Title: CTC-STOP: Utilising Circulating Tumour Cell (CTC) Counts to Optimize Systemic Therapy of Metastatic Prostate Cancer. | |||||||||||||
| Medical condition: Advanced Castration Resistant Prostate Cancer | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: GB (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-006958-31 | Sponsor Protocol Number: 2021/3401 | Start Date*: 2022-05-24 | 
| Sponsor Name:Gustave Roussy | ||
| Full Title: An Interventional and Translational Study investigating Sotorasib in Previously Treated Locally Advanced or Metastatic NSCLC Subjects With Mutated KRAS p.G12C | ||
| Medical condition: Locally-advanced and unresectable or metastatic non-small-cell lung cancer with KRAS G12C mutation | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-006372-17 | Sponsor Protocol Number: Field-Cancerization | Start Date*: 2022-02-15 | |||||||||||
| Sponsor Name:Muehlenkreiskliniken AoeR | |||||||||||||
| Full Title: Evaluation of clinical and immunological effects of PD-1 inhibition on actinic keratoses in patients with advanced or metastatic cutaneous squamous cell carcinoma in combination with a pronounced f... | |||||||||||||
| Medical condition: advanced or metastatic cutaneous squamous cell carcinoma | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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