- 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 1 of 7.
EudraCT Number: 2004-000723-15 | Sponsor Protocol Number: IP-REM-AC-01 inc. A1,D1,2,3,4,5; | Start Date*: 2004-11-15 | |||||||||||
Sponsor Name:Fresenius Biotech GmbH | |||||||||||||
Full Title: Two-arm, randomized (2:1), open-label phase II/III study in EpCAM positive cancer patients with symptomatic malignant ascites using paracentesis plus the tri-functional antibody removab (anti-EpCAM... | |||||||||||||
Medical condition: Cancer : Malignant Ascites | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) LT (Completed) GB (Completed) EE (Completed) LV (Completed) AT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-001700-39 | Sponsor Protocol Number: IP-REM-PK-01-EU | Start Date*: 2005-09-14 | |||||||||||
Sponsor Name:Fresenius Biotech GmbH | |||||||||||||
Full Title: Determination of systemic exposure and characterization of pharmacokinetics of the tri-functional antibody catumaxomab (anti-EpCAM X anti-CD3) administered intraperitoneally in EpCAM positive cance... | |||||||||||||
Medical condition: epithelial cell adhesion molecule (EpCAM) expressing tumors in patients with malignant ascites requiring therapeutic ascites puncture | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-018275-20 | Sponsor Protocol Number: UMCNONCO201001 | Start Date*: 2010-03-24 | ||||||||||||||||
Sponsor Name:University Medical Centre Nijmegen St Radboud | ||||||||||||||||||
Full Title: A phase II study of cediranib as palliative treatment in patients with symptomatic malignant ascites or pleural effusion | ||||||||||||||||||
Medical condition: symptomatic malignant ascites or pleural effusion | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-014076-22 | Sponsor Protocol Number: IP-CAT-AC-04 | Start Date*: 2009-09-23 | |||||||||||
Sponsor Name:Fresenius Biotech GmbH | |||||||||||||
Full Title: Phase II open label study to evaluate the safety of a second i.p. infusion cycle of catumaxomab in patients with malignant ascites due to carcinoma, requiring their first therapeutic puncture after... | |||||||||||||
Medical condition: Malignant Ascites | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FR (Ongoing) ES (Ongoing) IT (Completed) BE (Completed) SE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-001557-17 | Sponsor Protocol Number: IP-CAT-AC-03 | Start Date*: 2008-12-16 | |||||||||||
Sponsor Name:Fresenius Biotech GmbH | |||||||||||||
Full Title: Two-arm, randomized, open-label, phase IIIb study investigating the safety of a 3 hour i.p. infusion of catumaxomab with and without prednisolone premedication in patients with malignant ascites du... | |||||||||||||
Medical condition: malignant ascites | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) IT (Completed) FR (Ongoing) BE (Ongoing) GB (Completed) SE (Completed) NL (Ongoing) DK (Completed) PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-000604-16 | Sponsor Protocol Number: ARD6772 | Start Date*: 2006-08-30 |
Sponsor Name:sanofi-aventis recherche & développement | ||
Full Title: A Multicenter, Open-Label, Single-Arm Study of Intravenous AVE0005 (VEGF Trap) Administered Every 2 Weeks in Advanced Ovarian Cancer Patients with Recurrent Symptomatic Malignant Ascites. | ||
Medical condition: Advanced ovarian cancer patients with recurrent symptomatic malignant ascites. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: SE (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-005026-31 | Sponsor Protocol Number: EFC6125 [AVE0005A/3001] | Start Date*: 2006-04-24 |
Sponsor Name:Sanofi-Synthelabo Recherche, a subsidiary of sanofi-aventis group | ||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Arm Study of the Effect of Intravenous AVE0005 (VEGF Trap) Administered Every 2 Weeks in Advanced Ovarian Cancer Patients with ... | ||
Medical condition: pacientes con cáncer de ovario avanzado con ascitis maligna sintomática recurrente | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: ES (Completed) GB (Completed) HU (Completed) AT (Prematurely Ended) BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-014725-16 | Sponsor Protocol Number: AIO-SUP-0108 | Start Date*: 2010-01-14 | ||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:AIO Studien gGmbH | ||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Double-blind, placebo-controlled, randomized phase II-study investigating the efficacy of Bevacizumab for symptom control in patients with malignant ascites due to advanced-stage gastrointestinal c... | ||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: patients with malignant ascites due to advanced-stage gastro-intestinal cancers | ||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-003492-29 | Sponsor Protocol Number: 391402 | Start Date*: 2016-03-02 | |||||||||||
Sponsor Name:Baxalta Innovations GmbH | |||||||||||||
Full Title: A Phase 1/2a, Open-Label, Parallel, Two-Arm, Dose-Escalation Study to Assess the Safety, Tolerability, Efficacy, Pharmacokinetics, and Pharmacodynamics of BAX69 in Subjects with Refractory Ovarian... | |||||||||||||
Medical condition: Refractory Ovarian Cancer with Malignant Ascites | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: HU (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-005282-39 | Sponsor Protocol Number: AIRC-2013-144445 | Start Date*: 2014-05-22 | ||||||||||||||||
Sponsor Name:Fondazione IRCCS Istituto Nazionale dei Tumori di Milano | ||||||||||||||||||
Full Title: Effects of high Intra-abdominal pressure on tissue diffusion and pharmacokinectics of cisplatin during HIPEC | ||||||||||||||||||
Medical condition: patients affected by peritoneal carcinomatosis from colorectal cancer or pseudomyxoma peritonei | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004585-15 | Sponsor Protocol Number: Cat-Ovar_2011 | Start Date*: 2012-11-29 | |||||||||||
Sponsor Name:Charité - Universitätsmedizin Berlin | |||||||||||||
Full Title: Single –arm, multicenter phase-II trial for catumaxomab and chemotherapy in patients with recurrent ovarian cancer to investigate the feasibility and clinical activity of initial intraperitoneal ca... | |||||||||||||
Medical condition: This is an international, explorative, open-label, prospective, non-randomized multicenter phase II study to assess the feasibility and clinical activity of initial intraperitoneal catumaxomab foll... | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001429-25 | Sponsor Protocol Number: 2011.0704 | Start Date*: 2011-08-23 |
Sponsor Name:University Medical Center Groningen | ||
Full Title: Feasibility Study: FES-PET to determine ER-expression in epithelial ovarian cancer | ||
Medical condition: epithelial ovarian cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-022810-26 | Sponsor Protocol Number: PERCAT01 Version 10, 31.01.2011 | Start Date*: 2011-03-16 | |||||||||||||||||||||
Sponsor Name:University Witten/Herdecke | |||||||||||||||||||||||
Full Title: MULTICENTER, OPEN-LABEL PHASE II STUDY TO EVALUATE THE EFFICACY OF A 2-CYCLE IMMUNOTHERAPY WITH THE TRI FUNCTIONAL BISPECIFIC ANTIBODY CATUMAXOMAB (ANTI EPCAM X ANTI-CD3) IN ADDITION TO SYSTEMIC CH... | |||||||||||||||||||||||
Medical condition: PERITONEAL CARCINOMATOSIS FROM GASTRIC OR COLORECTAL ADENOCARCINOMA | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-001552-44 | Sponsor Protocol Number: TRIO 015 | Start Date*: 2008-09-29 | |||||||||||
Sponsor Name:Cancer International research Group | |||||||||||||
Full Title: A MULTICENTER OPEN LABEL PHASE II STUDY OF THE EFFICACY AND SAFETY OF AMG 479, A FULLY HUMAN MONOCLONAL ANTIBODY AGAINST INSULIN-LIKE GROWTH FACTOR TYPE 1 RECEPTOR (IGF-1R) AS SECOND LINE THERAPY I... | |||||||||||||
Medical condition: Recurrent Platinum-sensitive ovarian cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Completed) DE (Completed) ES (Prematurely Ended) IE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020787-37 | Sponsor Protocol Number: 8159 | Start Date*: 2013-01-28 |
Sponsor Name:Universitair Medisch Centrum Groningen | ||
Full Title: Neo-adjuvant chemotherapy, cytoreductive surgery with hyperthermic intra-peritoneal chemotherapy for peritoneal carcinomatosis of colorectal origin (NACHO-trial) | ||
Medical condition: peritoneal carcinomatosis of colorectal origin | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-001660-29 | Sponsor Protocol Number: FAB18 | Start Date*: 2019-01-16 | |||||||||||
Sponsor Name:Leiden University Medical Center | |||||||||||||
Full Title: FAB: Functional Analysis of BRCAness | |||||||||||||
Medical condition: Recurrent epithelial ovarian cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-003460-24 | Sponsor Protocol Number: 82914 | Start Date*: 2023-02-23 | |||||||||||
Sponsor Name:Radboud University Medical Center | |||||||||||||
Full Title: Pilot study to determine the intraTUMORal OsImertinib concentration in patients with peritoneal metastasizeD colorectal cancer (TUMOROID study) | |||||||||||||
Medical condition: Colorectal cancer | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-003427-36 | Sponsor Protocol Number: M10-898 | Start Date*: 2012-04-12 | |||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
Full Title: Randomized, Double-Blind, Multicenter, Phase 2 Trial Comparing Veliparib Plus Carboplatin and Paclitaxel Versus Placebo Plus Carboplatin and Paclitaxel in Previously Untreated Metastatic or Advance... | |||||||||||||
Medical condition: Metastatic or Advanced Non-Small-Cell Lung Cancer (NSCLC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) HU (Completed) SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000517-20 | Sponsor Protocol Number: CO-338-017 | Start Date*: 2013-11-26 | |||||||||||||||||||||
Sponsor Name:Clovis Oncology, Inc. | |||||||||||||||||||||||
Full Title: A Phase 2, Open-Label Study of Rucaparib in Patients with Platinum-Sensitive, Relapsed, High-Grade Epithelial Ovarian, Fallopian Tube, or Primary Peritoneal Cancer | |||||||||||||||||||||||
Medical condition: Platinum-Sensitive, Relapsed, High-Grade Epithelial Ovarian, Fallopian Tube, or Primary Peritoneal Cancer | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) ES (Completed) FR (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-003340-30 | Sponsor Protocol Number: GM307 | Start Date*: 2008-08-21 | |||||||||||
Sponsor Name:Genta Incorporated | |||||||||||||
Full Title: A multicenter, randomized, double-blind study of dacarbazine with or without Genasense in chemotherapy naïve subjects with advanced melanoma and low LDH (The AGENDA Trial) | |||||||||||||
Medical condition: Advanced Melanoma. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) FR (Ongoing) DE (Completed) CZ (Completed) ES (Ongoing) AT (Completed) IT (Ongoing) PL (Ongoing) | |||||||||||||
Trial results: (No results available) |
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