- Trials with a EudraCT protocol (34)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
34 result(s) found for: Proportional hazards model.
Displaying page 1 of 2.
EudraCT Number: 2013-001033-40 | Sponsor Protocol Number: VS-6063-202 | Start Date*: 2013-07-26 | |||||||||||
Sponsor Name:Verastem Inc | |||||||||||||
Full Title: A Phase II Randomized, Double-Blind, Placebo-Controlled, Multicenter Study of VS 6063 in Subjects with Malignant Pleural Mesothelioma | |||||||||||||
Medical condition: MPM is a rare but aggressive tumor of the serosal surfaces (specifically the pleura and peritoneum) that is highly invasive and progresses rapidly. The main risk factor is exposure to carcinogeni... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) BE (Completed) ES (Prematurely Ended) SE (Prematurely Ended) NL (Completed) NO (Completed) PL (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-003238-35 | Sponsor Protocol Number: 4_141221 | Start Date*: 2021-09-15 | |||||||||||
Sponsor Name:Oslo University Hospital | |||||||||||||
Full Title: Effects of supplemental oxygen on systemic and cerebral hemodynamics in experimental hypovolemia: A randomized, phase IV, crossover study to study the effect of supplemental oxygen vs. room air on ... | |||||||||||||
Medical condition: Hypovolemia is the condition under investigation. Hypovolemia is induced by the "lower body negative pressure" (LBNP)-model. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-004496-10 | Sponsor Protocol Number: NRL011-01/2004 | Start Date*: 2005-04-05 |
Sponsor Name:Norgine International Limited | ||
Full Title: A Phase 2a double blind, randomised, placebo controlled, two dose study to determine the effect of orally administered methylnaltrexone (MNTX) in preventing post-operative opiate induced constipati... | ||
Medical condition: Coated MNTX is being developed for the prevention of constipation in patients taking opioids for hip and knee replacement surgery for analgesia (pain relief). This drug is as yet unlicensed for use... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-002852-17 | Sponsor Protocol Number: GOG-0277 | Start Date*: 2013-03-13 | |||||||||||
Sponsor Name:EORTC | |||||||||||||
Full Title: A Phase III Randomised Trial of Gemcitabine plus Docetaxel followed by Doxorubicin versus observation for uterus-limited, high grade uterine leiomyosarcoma | |||||||||||||
Medical condition: Patients with high risk uterine LMS, FIGO stage I (confined to corpus +/- cervix). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) FR (Prematurely Ended) BE (Prematurely Ended) ES (Prematurely Ended) NL (Prematurely Ended) DE (Prematurely Ended) DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-002541-39 | Sponsor Protocol Number: 3005011 | Start Date*: 2005-08-24 | |||||||||||
Sponsor Name:Orion Corporation | |||||||||||||
Full Title: A Prospective, Multi-Centre, Randomised, Double-Blind Comparison of intravenous Dexmedetomidine with Propofol/Midazolam for continous sedation (24 hours to 14 days) of ventilated Patients in Intens... | |||||||||||||
Medical condition: Patients requiring mechanical ventilation and sedation in ICU. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000266-11 | Sponsor Protocol Number: 2012-772 | Start Date*: 2014-05-27 |
Sponsor Name:HOSPICES CIVILS DE LYON | ||
Full Title: Multicenter, randomized trial of carboplatin +/- paclitaxel in vulnerable elderly patients with stage III-IV advanced ovarian cancer. | ||
Medical condition: Vulnerable elderly women with newly diagnosed stage III-IV ovarian cancer after an initial debulking surgery or with a planned interval debulking surgery. | ||
Disease: | ||
Population Age: Elderly | Gender: Female | |
Trial protocol: IT (Completed) IE (Completed) DK (Prematurely Ended) FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-005601-37 | Sponsor Protocol Number: RBHP2015PICKERING4 | Start Date*: 2016-02-24 | |||||||||||
Sponsor Name:CHU Clermont-Ferrand | |||||||||||||
Full Title: IMPACT OF 5% LIDOCAINE MEDICATED PLASTER ON ALLODYNIC SYMPTOMS OF LOCALIZED NEUROPATHIC PAIN AFTER KNEE SURGERY. A prospective, randomized, placebo controlled study in parallel groups. | |||||||||||||
Medical condition: Post operative neuropathic pain (PONP) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003437-15 | Sponsor Protocol Number: P170922J | Start Date*: 2019-04-03 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS | |||||||||||||
Full Title: Rituximab from the FIRst Episode of Idiopathic Nephrotic Syndrome | |||||||||||||
Medical condition: Minimal Change Nephrotic Syndrome (MCNS) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001246-13 | Sponsor Protocol Number: TV3/001/06 | Start Date*: 2007-01-22 |
Sponsor Name:Oxford BioMedica UK Ltd. | ||
Full Title: Estudio internacional, aleatorizado, doble ciego, controlado con placebo y de grupos paralelos, para investigar si Trovax, añadido al tratamiento estándar de primera linea, prolonga la supervivenci... | ||
Medical condition: Locally advanced or metastatic renal clear cell adenocarcinoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) DE (Prematurely Ended) GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-000880-42 | Sponsor Protocol Number: HM14/10152 | Start Date*: 2014-11-12 | |||||||||||
Sponsor Name:University of Leeds | |||||||||||||
Full Title: GALACTIC: GA-101 (obinutuzumab) monocLonal Antibody as Consolidation Therapy In CLL | |||||||||||||
Medical condition: Chronic Lymphocytic Leukaemia (CLL). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003724-23 | Sponsor Protocol Number: GI-AU-NMH-2016-01 | Start Date*: 2017-12-28 | |||||||||||
Sponsor Name:The George Institute for Global Health, University of New South Wales | |||||||||||||
Full Title: Triple therapy prevention of Recurrent Intracerebral Disease EveNts Trial | |||||||||||||
Medical condition: Patients with a history of acute stroke due to Intracranial Haemorrhage with mild to moderately high blood pressure. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-005030-38 | Sponsor Protocol Number: PAT-CR-302 | Start Date*: 2019-08-10 | |||||||||||
Sponsor Name:Vifor Pharma, Inc. | |||||||||||||
Full Title: A Multicenter, Double-blind, Placebo-controlled, Randomized Withdrawal, Parallel Group Study of Patiromer for the Management of Hyperkalemia in Subjects Receiving Renin-Angiotensin-Aldosterone Syst... | |||||||||||||
Medical condition: Management of hyperkalemia due to renin-angiotension-aldosterone system medications in patients treated for heart failure. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) CZ (Completed) NL (Completed) ES (Ongoing) HU (Completed) DE (Completed) BG (Completed) GB (GB - no longer in EU/EEA) BE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000917-34 | Sponsor Protocol Number: 20-214-29/CA045-022 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Nektar Therapeutics | |||||||||||||
Full Title: A Phase 3, Randomized, Open-label Study to Compare Adjuvant Immunotherapy of Bempegaldesleukin Combined with Nivolumab Versus Nivolumab After Complete Resection of Melanoma in Patients at High Risk... | |||||||||||||
Medical condition: Resected Stage IIIA (lymph node metastasis > 1 mm)/B/C/D and IV melanoma with no evidence of disease | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) FR (Completed) GR (Completed) PL (Completed) AT (Completed) PT (Prematurely Ended) DE (Completed) NL (Completed) GB (GB - no longer in EU/EEA) IT (Prematurely Ended) RO (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001628-35 | Sponsor Protocol Number: X05140 | Start Date*: 2006-01-31 |
Sponsor Name:EBMT - CLWP | ||
Full Title: A randomized controlled study of Velcade (Bortezomib) plus Thalidomide plus Dexamethasone compared to Thalidomide plus Dexamethasone for the treatment of myeloma patients progressing or relapsing a... | ||
Medical condition: multiple myeloma patients in progression or relapse after autologous transplantation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) DE (Completed) GB (Completed) CZ (Completed) AT (Completed) HU (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-006713-16 | Sponsor Protocol Number: CP12-0604 | Start Date*: 2008-09-02 | |||||||||||
Sponsor Name:ImClone Systems Incorporated | |||||||||||||
Full Title: Phase II Randomized, Open-Label Study of IMC-1121B With or Without Dacarbazine in Patients with Metastatic Malignant Melanoma | |||||||||||||
Medical condition: Metastatic Malignant Melanoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006769-17 | Sponsor Protocol Number: TH0612 | Start Date*: 2007-04-18 | |||||||||||
Sponsor Name:Reckitt Benckiser Healthcare International Ltd | |||||||||||||
Full Title: A randomised, controlled, open-label, single-centre, parallel group, pilot study to investigate the onset of action of a lozenge compared with a caplet in patients with sore throat. | |||||||||||||
Medical condition: patients with sore throat | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002887-42 | Sponsor Protocol Number: EORTC-1612-MG | Start Date*: 2018-06-28 | |||||||||||
Sponsor Name:European Organisation for Research and Treatment of Cancer | |||||||||||||
Full Title: Combination of targeted therapy (encorafenib and binimetinib) followed by combination of immunotherapy (ipilimumab and nivolumab) vs immediate combination of immunotherapy in patients with unresect... | |||||||||||||
Medical condition: BRAF V600 mutation–positive unresectable or metastatic melanoma. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) GB (GB - no longer in EU/EEA) DE (Trial now transitioned) PL (Trial now transitioned) NL (Trial now transitioned) DK (Completed) ES (Ongoing) IT (Trial now transitioned) FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-005684-32 | Sponsor Protocol Number: | Start Date*: 2015-12-30 | |||||||||||
Sponsor Name:The Royal Marsden NHS Foundation Trust | |||||||||||||
Full Title: [18F] DIHYDRO-TESTOSTERONE PET IMAGING IN PATIENTS WITH PROGRESSIVE PROSTATE CANCER | |||||||||||||
Medical condition: Progressive Prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003916-29 | Sponsor Protocol Number: TREASURE | Start Date*: 2020-06-25 | |||||||||||
Sponsor Name:Frankfurter Institut für Klinische Krebsforschung IKF GmbH at Krankenhaus Nordwest | |||||||||||||
Full Title: - TREASURE- Thoracic RadiothErapy with Atezolizumab in Small cell lUng canceR Extensive disease: a randomized, open-label, multicenter phase II study | |||||||||||||
Medical condition: Small cell lung cancer extensive disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-020452-64 | Sponsor Protocol Number: version2.0 | Start Date*: 2010-10-05 | |||||||||||
Sponsor Name:Hull and East Yorkshire Hospitals NHS Trust | |||||||||||||
Full Title: A prospective randomisd open label study to determine the effects of intravenous iron administration on markers of acute kidney injury in chronic kidney disease (CKD) | |||||||||||||
Medical condition: patients with known chonic kidney disease with functional or absolute Iron deficiency Anaemia, and are greater than 18 years will be given repleacement iron therapy accoring to current local protoc... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
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