- Trials with a EudraCT protocol (368)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
368 result(s) found for: Urine dipstick.
Displaying page 1 of 19.
EudraCT Number: 2007-003894-18 | Sponsor Protocol Number: M07CCL | Start Date*: 2008-01-30 |
Sponsor Name:NKI-AVL | ||
Full Title: Open-label, randomised, multi-center study investigating Cetuximab, in combination with concurrent chemo- / radiotherapy in locally advanced non-small cell lung carcinoma | ||
Medical condition: Non-small cell lung cancer locally advanced | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-004824-19 | Sponsor Protocol Number: ML21206 | Start Date*: 2008-08-08 |
Sponsor Name:Roche Austria GmbH | ||
Full Title: Bevacizumab in Chronic Lymphocytic Leukemia: a proof of concept study | ||
Medical condition: Chronic Lymphocytic Leukemia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2008-002902-20 | Sponsor Protocol Number: ML21901 | Start Date*: 2008-10-15 |
Sponsor Name:Onkološki inštitut Ljubljana | ||
Full Title: Preoperative Radiotherapy with Capecitabine and Bevacizumab in locally advanced rectal cancer: CRAB Phase II study | ||
Medical condition: Locally advanced rectal cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: | |
Trial protocol: SI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-006161-13 | Sponsor Protocol Number: ML19983 | Start Date*: 2007-06-22 |
Sponsor Name:Roche Pharma AG | ||
Full Title: A single arm Phase II study to assess efficacy and safety of bevacizumab in combination with the standard therapy (interferon alfa-2a and vinblastine) as first-line treatment for patients with meta... | ||
Medical condition: Metastatic renal cell cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-005887-97 | Sponsor Protocol Number: MO19390 | Start Date*: 2006-07-06 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: Open-label study of bevacizumab (AVASTIN®) in combination with platinum-containing chemotherapy as first-line treatment of patients with advanced or recurrent non-squamous non-small cell lung cancer | |||||||||||||
Medical condition: Advanced or recurrent non-squamous non-small cell lung cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SI (Completed) FI (Completed) SE (Completed) ES (Completed) NL (Completed) AT (Completed) CZ (Completed) EE (Completed) DE (Completed) LT (Completed) HU (Completed) SK (Completed) GB (Completed) PT (Completed) DK (Completed) LV (Completed) IS (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001443-39 | Sponsor Protocol Number: 167700-004CL | Start Date*: 2016-09-23 | |||||||||||
Sponsor Name:Proximagen Ltd. | |||||||||||||
Full Title: A Randomised, Parallel Arm, Placebo-Controlled, Double-Blind, Study of the Safety and Efficacy of PRX167700 Added to Existing Non-steroidal Anti-inflammatory Therapy in Adults with Moderate-to-Seve... | |||||||||||||
Medical condition: Osteoarthritis of the knee | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) HU (Completed) CZ (Completed) PL (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000026-31 | Sponsor Protocol Number: ML18704 | Start Date*: 2006-06-20 |
Sponsor Name:Roche Austria GmbH | ||
Full Title: Bevacizumab as treatment for patients with relapsed/refractory multiple myeloma | ||
Medical condition: Multiple myeloma, relapsed/refractory after at least 2 lines of prior therapy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2007-002886-11 | Sponsor Protocol Number: BEBYP | Start Date*: 2008-01-14 | |||||||||||
Sponsor Name:G.O.N.O. - GRUPPO ONCOLOGICO NORD OVEST | |||||||||||||
Full Title: AN OPEN-LABEL, MULTICENTER, RANDOMIZED PHASE III STUDY OF SECOND-LINE CHEMOTHERAPY WITH OR WITHOUT BEVACIZUMAB IN METASTATIC COLORECTAL CANCER PATIENTS WHO HAVE RECEIVED FIRST-LINE CHEMOTHERAPY PLU... | |||||||||||||
Medical condition: METASTATIC COLORECTAL CANCER PATIENTS | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-006051-40 | Sponsor Protocol Number: Beva2007 | Start Date*: 2008-09-09 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA SENESE | |||||||||||||
Full Title: A PHASE II STUDY: UNOPERABLE NON NON SQUAMOUS NON SMALL CELL LUNG CANCER METRONOMIC BIOCHEMOTHERAPY WITH WEEKLY CISPLATIN, DAILY ORAL ETOPOSIDE AND BEVACIZUMAB (mPEBev regimen) | |||||||||||||
Medical condition: Patients with UNOPERABLE NON NON SQUAMOUS NON SMALL CELL LUNG CANCER | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-003006-34 | Sponsor Protocol Number: ML21744 | Start Date*: 2008-07-03 |
Sponsor Name:Oslo Universitetssykehus | ||
Full Title: A multicenter, randomized, phase II clinical trial to evaluate the effect of Avastin in combination with neoadjuvant treatment regimens on the molecular and metabolic characteristics and changes in... | ||
Medical condition: HER2 negative breast cancer | ||
Disease: | ||
Population Age: | Gender: Male, Female | |
Trial protocol: NO (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-002529-21 | Sponsor Protocol Number: MO19391 | Start Date*: 2006-09-05 |
Sponsor Name:F.Hoffmann-La Roche Ltd | ||
Full Title: Open-label study of bevacizumab (Avastin®) plus taxane monotherapy or in combination for the first-line treatment of patients with locally recurrent or metastatic breast cancer | ||
Medical condition: Locally recurrent or metastatic breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) NL (Completed) ES (Completed) EE (Completed) AT (Completed) CZ (Completed) DE (Completed) LT (Completed) LV (Completed) SI (Completed) HU (Completed) SE (Completed) SK (Completed) PT (Completed) IT (Completed) GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-002716-27 | Sponsor Protocol Number: ALN-CC5-005 | Start Date*: 2019-06-11 |
Sponsor Name:Alnylam Pharmaceuticals Inc | ||
Full Title: A Phase 2, Randomized, Double-blind, Placebo-controlled Study of Cemdisiran in Adult Patients with IgA Nephropathy | ||
Medical condition: Immunoglobulin A nephropathy (IgAN) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) SE (Prematurely Ended) ES (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2010-022520-73 | Sponsor Protocol Number: CT/10.15 | Start Date*: 2011-07-12 |
Sponsor Name:Hellenic Oncology Research Group | ||
Full Title: Phase II, open-label non-randomized trial to investigate the efficacy of Bevacizumab in combination with dose dense sequential chemotherapy in the neo-adjuvant setting for HER2 negative breast canc... | ||
Medical condition: Early breast cancer (primary operable HER2-negative breast cancer) | ||
Disease: | ||
Population Age: | Gender: Female | |
Trial protocol: GR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-004833-70 | Sponsor Protocol Number: BUSAL-III-08-1 | Start Date*: 2009-01-16 | |||||||||||
Sponsor Name:Laboratoires SMB S.A. | |||||||||||||
Full Title: A phase III, randomized, parallel group, open study to compare the therapeutic efficacy and safety of SMB BUDESONIDE-SALMETEROL DPI capsule 150/25μg BID delivered by the AXAHALER® versus SYMBICORT®... | |||||||||||||
Medical condition: Patients with moderate to severe persistent asthma. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-001537-10 | Sponsor Protocol Number: ASL608LIOM04 | Start Date*: 2008-05-14 | |||||||||||
Sponsor Name:G.O.N.O. - GRUPPO ONCOLOGICO NORD OVEST | |||||||||||||
Full Title: A PHASE III RANDOMIZED TRIAL OF FOLFOXIRI + BEVACIZUMAB VERSUS FOLFIRI + BEVACIZUMAB AS FIRST-LINE TREATMENT FOR METASTATIC COLORECTAL CANCER | |||||||||||||
Medical condition: colorectal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004983-30 | Sponsor Protocol Number: ACO-ASSO LM1 | Start Date*: 2006-11-03 |
Sponsor Name:ACO-ASSO | ||
Full Title: Pre- and postoperative chemotherapy including Bevacizumab in potentially curable metastatic colorectal Cancer (mCRC). A multicenter, prospective Phase I/II academic trial. | ||
Medical condition: Patients with histologically confirmed diagnosis of metastatic Colorectal Cancer (CRC) including potentially resectable liver metastases, untreated yet with chemotherapy for metastatic disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-004748-22 | Sponsor Protocol Number: ML20058 | Start Date*: 2006-12-14 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA S. LUIGI GONZAGA | |||||||||||||
Full Title: phase II study of the combination of bevacizumab plus somatostatin analogue and metronomic capecitabine as first-line therapy in patients with advanced inoperable well-differentiated neuroendrocri... | |||||||||||||
Medical condition: Patients with Advanced Inoperable Well-Differentiated Neuroendocrine Tumors | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011377-33 | Sponsor Protocol Number: 08_CLPHA_55 | Start Date*: 2009-06-25 | |||||||||||
Sponsor Name:The Christie NHS Foundation Trust | |||||||||||||
Full Title: AN ASSESSMENT OF IMAGING AND CIRCULATING BIOMARKERS IN PATIENTS WITH METASTATIC COLORECTAL CARCINOMA TREATED WITH THE ANTI-VEGF MONOCLONAL ANTIBODY BEVACIZUMAB | |||||||||||||
Medical condition: Metastatic colorectal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001517-15 | Sponsor Protocol Number: ML 19309 | Start Date*: 2006-10-26 | |||||||||||
Sponsor Name:ROCHE | |||||||||||||
Full Title: Italian multicenter phase II trial using Fotemustine plus Bevacizumab as first-line therapy in metastatic melanoma. | |||||||||||||
Medical condition: Patients with stage IV melanoma, previously untreated with chemo- or immuno-therapy for metastatic disease, will be eligible for the study. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004429-27 | Sponsor Protocol Number: ONC-2006-003 | Start Date*: 2007-05-25 | |||||||||||
Sponsor Name:ISTITUTO CLINICO HUMANITAS | |||||||||||||
Full Title: Phase II study of the combination of bevacizumab plus pemetrexed and carboplatin as first-line therapy in patients with malignant pleural mesothelioma | |||||||||||||
Medical condition: Histologically proven diagnosis of malignant pleural mesothelioma. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
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