- Trials with a EudraCT protocol (127)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
127 result(s) found for: Malignant ascites.
Displaying page 4 of 7.
EudraCT Number: 2007-007633-39 | Sponsor Protocol Number: MORAb-009-002 | Start Date*: 2008-04-03 | |||||||||||
Sponsor Name:Morphotek, Inc. | |||||||||||||
Full Title: Estudio fase 2 aleatorizado, controlado con placebo, de doble ciego sobre la eficacia de MORAb-009 en combinación con gemcitabina en pacientes con cáncer de páncreas avanzado | |||||||||||||
Medical condition: Español: Cáncer de páncreas avanzado en pacientes con enfermedad no extirpable que no han recibido quimioterapia o radioterapia previa para el cáncer de páncreas. Ingles : Advanced pancreatic can... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DE (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001149-14 | Sponsor Protocol Number: A6181034 | Start Date*: 2004-09-27 | |||||||||||
Sponsor Name:PFIZER | |||||||||||||
Full Title: A Phase 3, Randomized Study of SU011248 versus Interferon-a as First-Line Systemic Therapy for Patients with Metastatic Renal Cell Carcinoma. | |||||||||||||
Medical condition: metastatic renal cell carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) ES (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003118-26 | Sponsor Protocol Number: RAMSES/FLOT7 | Start Date*: 2016-04-26 | |||||||||||
Sponsor Name:Institut für Klinische Krebsforschung IKF GmbH at Krankenhaus Nordwest | |||||||||||||
Full Title: RAMSES / FLOT7 Perioperative RAMucirumab in combination with FLOT versus FLOT alone for reSEctable eSophagogastric adenocarcinoma RAMSES - a phase II/III trial of the AIO | |||||||||||||
Medical condition: locally advanced resectable adenocarcinoma of the esophagogastric junction or the stomach | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-001087-36 | Sponsor Protocol Number: Bay43-9006/12414 | Start Date*: 2008-08-18 | |||||||||||
Sponsor Name:Bayer Healthcare AG | |||||||||||||
Full Title: A Phase III randomized, double-blind, placebo-controlled study of sorafenib as adjuvant treatment for hepatocellular carcinoma after surgical resection or local ablation. | |||||||||||||
Medical condition: To evaluate the clinical benefit of sorafenib vs placebo as adjuvant treatment in subjects with HCC who received potentially curative treatment (surgical resection or local ablation). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) GB (Completed) ES (Completed) AT (Completed) BE (Completed) FR (Completed) IT (Completed) PT (Completed) DE (Completed) GR (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002041-36 | Sponsor Protocol Number: POLARIS2009-001 | Start Date*: 2011-11-15 | |||||||||||
Sponsor Name:Polaris Group | |||||||||||||
Full Title: A Randomized, Double-Blind, Multi-Center Phase 3 Study of ADI-PEG 20 Plus Best Supportive Care (BSC) Versus Placebo Plus BSC in Subjects With Advanced Hepatocellular Carcinoma (HCC) Who Have Fai... | |||||||||||||
Medical condition: Advanced Hepatocellular Carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) IT (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-001451-21 | Sponsor Protocol Number: A4061032 | Start Date*: 2008-06-18 | |||||||||||
Sponsor Name:Pfizer Inc.,235 East 42nd Street,New York,NY 10017 | |||||||||||||
Full Title: AXITINIB (AG-013736) AS SECOND LINE THERAPY FOR METASTATIC RENAL CELL CANCER: AXIS TRIAL | |||||||||||||
Medical condition: Renal cell carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) ES (Completed) AT (Completed) FR (Completed) GB (Completed) IE (Completed) DE (Completed) IT (Completed) PL (Completed) GR (Completed) SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000934-53 | Sponsor Protocol Number: 104-13-302 | Start Date*: 2014-11-11 | |||||||||||
Sponsor Name:Celsion Corporation | |||||||||||||
Full Title: A Phase III, Randomized, Double Blind, Dummy-Controlled Study of ThermoDox® (Lyso-Thermosensitive Liposomal Doxorubicin-LTLD) in Hepatocellular Carcinoma (HCC) using standardized Radiofrequency Abl... | |||||||||||||
Medical condition: Hepatocellular Carcinoma (HCC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003847-66 | Sponsor Protocol Number: H6Q-MC-S061 | Start Date*: 2008-03-28 |
Sponsor Name:Eli Lilly and company | ||
Full Title: Dose Finding and Randomized, Multicenter, Placebo-Controlled, Phase 2 Study of Enzastaurin and Sunitinib versus Placebo and Sunitinib in Patients with Metastatic Renal Cell Carcinoma | ||
Medical condition: Renal cell carcinoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) AT (Completed) PL (Completed) IT (Completed) ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-002929-35 | Sponsor Protocol Number: CFGF401X2101 | Start Date*: 2015-01-02 | ||||||||||||||||
Sponsor Name:Novartis Farmacéutica, S.A. | ||||||||||||||||||
Full Title: A phase I/II, multicenter, open-label study of oral FGF401 in adult patients with hepatocellular carcinoma or solid malignancies characterized by positive FGFR4 and KLB expression | ||||||||||||||||||
Medical condition: Hepatocellular carcinoma or other solid tumors characterized by positive FGFR4 and KLB expression | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) DE (Prematurely Ended) FR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-011305-17 | Sponsor Protocol Number: CA046 | Start Date*: 2011-08-18 | |||||||||||
Sponsor Name:Abraxis BioScience, LLC, a wholly-owned subsidiary of Celgene Corporation | |||||||||||||
Full Title: A Randomized Phase III Study of Weekly ABI-007 plus Gemcitabine versus Gemcitabine Alone in Patients with Metastatic Adenocarcinoma of the Pancreas | |||||||||||||
Medical condition: Metastatic Adenocarcinoma of the Pancreas | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) ES (Completed) BE (Completed) AT (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-004273-28 | Sponsor Protocol Number: EORTC 08031 | Start Date*: 2005-11-15 | |||||||||||
Sponsor Name:European Organisation for Research and Treatment of Cancer | |||||||||||||
Full Title: A phase II feasibility trial of induction chemotherapy followed by extrapleural pneumonectomy and postoperative radiotherapy in patients with malignant pleural mesothelioma. | |||||||||||||
Medical condition: malignant pleural mesothelioma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-016725-34 | Sponsor Protocol Number: C18083/2048 | Start Date*: 2010-05-21 | |||||||||||
Sponsor Name:Cephalon, Inc. | |||||||||||||
Full Title: An Open-Label Study to Evaluate the Efficacy and Safety of Treatment With Bendamustine in Combination With Ofatumumab in Previously Untreated Patients With Indolent B-Cell Non-Hodgkin’s Lymphoma (NHL) | |||||||||||||
Medical condition: Non-Hodgkin’s Lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005473-29 | Sponsor Protocol Number: FL-OSHO/GLSG-M3-2005-01 | Start Date*: 2007-03-28 | |||||||||||
Sponsor Name:Klinikum der Ludwig-Maximilians-Universität München, Klinikum Großhadern | |||||||||||||
Full Title: Randomisierte Phase III-Studie zur Primärtherapie von fortgeschrittenen follikulären Lymphomen bei älteren Patienten (>65 J.) und jüngeren Patienten, die nicht für eine Hochdosistherapie mit autolo... | |||||||||||||
Medical condition: Fortgeschrittene follikuläre Lymphome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001276-38 | Sponsor Protocol Number: ColoAd1-2001 | Start Date*: 2015-10-15 | |||||||||||
Sponsor Name:PsiOxus Therapeutics Ltd | |||||||||||||
Full Title: A Clinical Study Of ColoAd1 Administered Intraperitoneally: Dose Finding and Proof of Concept in Platinum-Resistant Epithelial Ovarian Cancer | |||||||||||||
Medical condition: Epithelial ovarian cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000736-21 | Sponsor Protocol Number: HLX01-FL03 | Start Date*: 2020-07-02 | |||||||||||
Sponsor Name:Shanghai Henlius Biotech Inc. | |||||||||||||
Full Title: A Phase 3 Multi-Centre, Randomised, Double-Blind, Parallel-Arm Study to Evaluate the Efficacy and Safety of HLX01 Versus Rituximab (Mabthera®) as First Line Treatment in Patients With Low Tumour Bu... | |||||||||||||
Medical condition: Low tumour burden follicular lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000004-33 | Sponsor Protocol Number: IPR/18 | Start Date*: 2008-10-13 | |||||||||||
Sponsor Name:MOLMED | |||||||||||||
Full Title: NGR012: A phase II study of NGR-hTNF administered in combination with doxorubicin every 3 weeks in patients affected by advanced or metastatic ovarian cancer | |||||||||||||
Medical condition: Patients affected by advanced or metastatic ovarian cancer previously treated with platinum regimens (cis or carboplatin) plus paclitaxel | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002531-29 | Sponsor Protocol Number: NaturalDCformCRPC | Start Date*: 2014-10-30 |
Sponsor Name:Radboud University Medical Centre Nijmegen | ||
Full Title: A randomized phase IIa study: natural dendritic cells for immunotherapy of chemo-naive metastatic castration-resistant prostate cancer patients | ||
Medical condition: Asymptomatic or minimally symptomatic, chemo-naive mCRPC patients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-000591-42 | Sponsor Protocol Number: JX594-IV-HEP021 | Start Date*: 2012-09-21 | |||||||||||
Sponsor Name:Jennerex, Inc | |||||||||||||
Full Title: A Single-Arm, Open-Label Phase 2 Study of JX 594 (Thymidine Kinase-Deactivated Vaccinia Virus plus GM-CSF) Administered by Weekly Intravenous (IV) Infusions in Sorafenib-naïve Patients with Advance... | |||||||||||||
Medical condition: Advanced Hepatocellular Carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000193-35 | Sponsor Protocol Number: MONAVI-1 | Start Date*: 2015-10-01 | |||||||||||
Sponsor Name:Centre François Baclesse | |||||||||||||
Full Title: A phase II study of ABT-263 as single agent in women with platinum resistant/refractory recurrent ovarian cancer | |||||||||||||
Medical condition: Platinum-resistant or refractory ovarian cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004299-38 | Sponsor Protocol Number: ESPAC-4Version:7Date:21/07/2011 | Start Date*: 2008-09-17 | ||||||||||||||||
Sponsor Name:The University of Liverpool [...] | ||||||||||||||||||
Full Title: European Study Group for Pancreatic Cancer - Trial 4. Combination versus single agent chemotherapy in resectable pancreatic ductal and peri-ampullary cancers. | ||||||||||||||||||
Medical condition: Resectable pancreatic or peri-ampullary cancers | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) SE (Restarted) FI (Prematurely Ended) DE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
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