- Trials with a EudraCT protocol (113)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
113 result(s) found for: Malignant Hypertension.
Displaying page 1 of 6.
EudraCT Number: 2012-002927-14 | Sponsor Protocol Number: AGO/2012/004 | Start Date*: 2013-07-10 | |||||||||||
Sponsor Name:University Ghent | |||||||||||||
Full Title: Dosistitratie van lisinopril bij kinderen van 1 tot 18 jaar met primaire of secundaire hypertensie | |||||||||||||
Medical condition: Hypertensie | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001863-35 | Sponsor Protocol Number: THAM | Start Date*: 2016-06-21 |
Sponsor Name:Universitätsklinik für Klinische Pharmakologie, Medizinische Universität Wien | ||
Full Title: Effects of Tromethamine on Cerebral Oxygenation and Metabolism in Patients Suffering Intractable Intracranial Hypertension – an exploratory study. | ||
Medical condition: Critically ill patients (SAH, ICB, AVM bleedings, malignant MCA infarcts) under sedation and mechanical ventilation in need of multimodality monitoring, including brain tissue oxygen monitoring and... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2012-001020-35 | Sponsor Protocol Number: 94070C | Start Date*: 2012-12-05 | |||||||||||
Sponsor Name:Helse Bergen HF, Haukeland University Hospital | |||||||||||||
Full Title: A randomized phase II trial comparing bevacizumab monotherapy with dacarbazine (DTIC) in treatment of malignant melanoma, focusing on angiogenic markers and prevention of hypertension. | |||||||||||||
Medical condition: Previously treated or untreated histologically confirmed metastatic and unresectable melanoma with radiological (RECIST), clinical or biochemical progressive disease. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001861-40 | Sponsor Protocol Number: BRTA-0100-015 (EORTC 62061) | Start Date*: 2006-09-21 | |||||||||||
Sponsor Name:SYSTEMS MEDICINE, LLC | |||||||||||||
Full Title: Randomized phase II study of brostallicin (PNU-166196A) versus doxorubicin as first line chemotherapy in patients with advanced or metastatic soft tissue sarcoma | |||||||||||||
Medical condition: Advanced or metastatic soft tissue sarcoma. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) GB (Completed) NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002695-34 | Sponsor Protocol Number: CS-201 | Start Date*: 2009-01-23 | |||||||||||
Sponsor Name:Kringle Pharma Europe AB | |||||||||||||
Full Title: A Phase I/II Double-Blind, Dose Ranging, Vehicle Controlled, Randomized, Parallel Groups, Safety, Tolerability and Efficacy Study of ChronSeal® (5-amino-acid deleted recombinant human Hepatocyte Gr... | |||||||||||||
Medical condition: Non-malignant full skin chronic venous leg ulcers of an area 3 - 20 cm2. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-000053-30 | Sponsor Protocol Number: A4061016 | Start Date*: 2005-07-21 | |||||||||||
Sponsor Name:Pfizer Inc. - La Jolla laboratories | |||||||||||||
Full Title: A randomized phase 2 study of the anti-angiogenesis agent AG-013736 in combination with gemcitabine in patients with chemotherapy-naïve advanced pancreatic cancer preceded by a phase 1 portion | |||||||||||||
Medical condition: Treatment of patients with chemotherapy-naïve, locally advanced or metastatic epithelial cancer of the exocrine pancreas | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) BE (Completed) DE (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005993-39 | Sponsor Protocol Number: IPR/16 | Start Date*: 2007-04-26 | |||||||||||
Sponsor Name:MOLMED | |||||||||||||
Full Title: NGR010: A phase II study of NGR-hTNF administered as single agent every 3 weeks in patients affected by advanced or metastatic malignant pleural mesothelioma previously treated with no more than on... | |||||||||||||
Medical condition: patients affected by advanced or metastatic malignant pleural mesothelioma previously treated with no more than one systemic therapeutic | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004909-33 | Sponsor Protocol Number: LCTU122 | Start Date*: 2015-09-21 | ||||||||||||||||
Sponsor Name:Manchester University NHS Foundation Trust | ||||||||||||||||||
Full Title: Thrombin Inhibition Preoperatively in Early Breast Cancer | ||||||||||||||||||
Medical condition: Breast Cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002525-29 | Sponsor Protocol Number: UC-0140/1206 | Start Date*: 2013-03-08 | |||||||||||
Sponsor Name:UNICANCER | |||||||||||||
Full Title: A phase II trial evaluating the Activity of Abiraterone Acetate plus Prednisone in Patients with a Molecular Apocrine HER2-negative locally advanced or metastatic Breast Cancer. | |||||||||||||
Medical condition: Molecular apocrine locally advanced or metastatic breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000774-58 | Sponsor Protocol Number: E7050-703 | Start Date*: 2012-01-30 | ||||||||||||||||
Sponsor Name:Eisai Inc. | ||||||||||||||||||
Full Title: An Open-Label, Multicenter, Randomized, Phase Ib/II Study of E7050 in Combination with Cisplatin and Capecitabine versus Cisplatin and Capecitabine Alone in Patients with Advanced or Metastatic Sol... | ||||||||||||||||||
Medical condition: Advanced or metastatic solid tumors and previously untreated gastric cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-003043-29 | Sponsor Protocol Number: MITO-16/MaNGO-OV2 | Start Date*: 2012-09-24 | |||||||||||
Sponsor Name:ISTITUTO NAZIONALE PER LO STUDIO E LA CURA DEI TUMORI - FONDAZIONE "G. PASCALE" | |||||||||||||
Full Title: A multicenter study in patients with stage III-IV epithelial ovarian cancer treated with carboplatin/paclitaxel with bevacizumab: clinical and biological prognostic factors | |||||||||||||
Medical condition: advanced ovarian cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001770-19 | Sponsor Protocol Number: TUD-SplusL-061 | Start Date*: 2014-09-01 | |||||||||||
Sponsor Name:Technische Universität Dresden | |||||||||||||
Full Title: 6 month, multi-center, open-label, prospective, randomized trial, investigating a standard regimen of an advagraf based immunosuppressive regimen in de-novo renal transplant patients versus a sl... | |||||||||||||
Medical condition: patients, waiting for first or second renal transplantation de novo kidney transplant patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-007792-24 | Sponsor Protocol Number: 1.1 | Start Date*: 2009-03-13 |
Sponsor Name:Medical University of Graz, Department of Internal Medicine, Div. Endocrinology and Nuclear Medicine | ||
Full Title: Effects of vitamin D supplementation in healthy women and men on immunological, endocrine and metabolic parameters | ||
Medical condition: Healthy volunteers. The intended indication for the product under development is prevention and treatment of immunological (e.g. type 1 diabetes), endocrine (e.g. endocrine hypertension) metabolic ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-005732-27 | Sponsor Protocol Number: UCSC-OM-SU-01 | Start Date*: 2006-12-21 | |||||||||||
Sponsor Name:Policlinico Universitario Agustino Gemelli | |||||||||||||
Full Title: EFFICACY AND SAFETY OF THE MULTITARGET INHIBITOR AGENT SU11248 IN PATIENTS WITH LOCALLY ADVANCED OR METASTATIC HEPATOCELLULAR CARCINOMA | |||||||||||||
Medical condition: Advanced (localized disease but surgically unresectable or metastatic) histologically/cytologically proven hepatocellular carcinoma (or hepatic lesion and aFP ³ 400 ng/ml). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) IT (Completed) | |||||||||||||
Trial results: (No results available) |
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: 2009-017485-23 | Sponsor Protocol Number: EORTC90091-10093 | Start Date*: 2013-04-24 | |||||||||||
Sponsor Name:EORTC | |||||||||||||
Full Title: TRastuzumab in HER2-negative Early breast cancer as Adjuvant Treatment for Circulating Tumor Cells (CTC) ("Treat CTC" trial) | |||||||||||||
Medical condition: HER2-Negative Early Breast Cancer | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) FR (Completed) GB (Completed) DE (Completed) GR (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002069-22 | Sponsor Protocol Number: ET17-057 | Start Date*: 2018-04-18 | |||||||||||
Sponsor Name:CENTRE LEON BERARD | |||||||||||||
Full Title: BREASTIMMUNE02 - A multicenter, randomized, open-label, Phase II trial aiming to evaluate the impact of pegfilgrastim on trastuzumab anti-tumor effect and antibody-dependent cell-mediated cytotoxic... | |||||||||||||
Medical condition: Operable HER2 positive breast cancer | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001568-66 | Sponsor Protocol Number: A4061028 | Start Date*: 2007-08-27 | ||||||||||||||||
Sponsor Name:Pfizer Inc, 235 East 42nd Street, New York, NY 10017, USA | ||||||||||||||||||
Full Title: A randomized, double-blind phase 3 study of gemcitabine plus AG-013736 versus gemcitabine plus placebo for the first-line treatment of patients with locally advanced, unresectable or metastatic pan... | ||||||||||||||||||
Medical condition: Unresectable or metastatic pancreatic cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IE (Prematurely Ended) SE (Completed) GB (Prematurely Ended) FR (Completed) PT (Completed) AT (Prematurely Ended) HU (Completed) BE (Completed) ES (Completed) CZ (Completed) IT (Prematurely Ended) DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-000961-10 | Sponsor Protocol Number: NITRO Protocol | Start Date*: 2011-12-07 | |||||||||||
Sponsor Name:Royal Liverpool and Broadgreen University Hospitals Trust | |||||||||||||
Full Title: Neoadjuvant IntraviTreal Ranibizumab treatment in high risk Ocular melanoma patients: A two stage single centre Phase II single arm study (NITRO Trial) | |||||||||||||
Medical condition: Uveal Melanoma (requiring enucleation) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020385-13 | Sponsor Protocol Number: 52702928 | Start Date*: 2010-06-21 | |||||||||||
Sponsor Name:Vejle Hospital | |||||||||||||
Full Title: Randomized phase II trial of combination chemotherapy with panitumumab or bevacizumab for patients with inoperable cholangiocarcinoma without KRAS mutations | |||||||||||||
Medical condition: Inoperable cholangiocarcinoma without KRAS mutations | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) SE (Completed) | |||||||||||||
Trial results: View results |
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