- Trials with a EudraCT protocol (13)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
13 result(s) found for: Catumaxomab.
Displaying page 1 of 1.
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: 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: 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: 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 (Completed) GB (Completed) SE (Completed) NL (Ongoing) DK (Completed) PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-018478-19 | Sponsor Protocol Number: GEICO-1001 | Start Date*: 2010-06-07 |
Sponsor Name:Grupo Español de Investigación en Cáncer de Ovario - GEICO | ||
Full Title: Ensayo fase II para evaluar la eficacia y seguridad de catumaxomab como tratamiento de consolidación en pacientes con un cáncer epitelial de ovario en una segunda o tercera remisión completa | ||
Medical condition: eficacia y seguridad de catumaxomab como tratamiento de consolidación en pacientes con un cáncer epitelial de ovario en una segunda o tercera remisión completa | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-002727-16 | Sponsor Protocol Number: IP-CAT-GC-03 | Start Date*: 2007-03-06 | |||||||||||
Sponsor Name:Fresenius Biotech GmbH | |||||||||||||
Full Title: Multicenter, open-label phase II study to evaluate the safety and efficacy of the tri-functional bispecific antibody catumaxomab (anti-EpCAM x anti-CD3) in patients with gastric adenocarcinoma afte... | |||||||||||||
Medical condition: Gastric Neoplasm malignant | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-005945-20 | Sponsor Protocol Number: IP-REM-GC-02 | Start Date*: 2006-06-08 | |||||||||||
Sponsor Name:Fresenius Biotech GmbH | |||||||||||||
Full Title: Multicenter, open-label and randomized phase II study to evaluate safety and efficacy of the tri-functional bispecific antibody catumaxomab(anti-EpCAM x anti-CD3) in patients after curative resecti... | |||||||||||||
Medical condition: Advanced gastric adenocarcinoma and intended curative gastrectomy (R0 resection). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
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 (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004484-54 | Sponsor Protocol Number: IP-CAT-OC-02 | Start Date*: 2007-08-30 | ||||||||||||||||||||||||||
Sponsor Name:Fresenius Biotech GmbH | ||||||||||||||||||||||||||||
Full Title: Multicenter, single-arm, phase II study of the tri functional antibody catumaxomab (anti EpCAM x anti-CD3) administered intra- and postoperatively in patients with epithelial ovarian cancer | ||||||||||||||||||||||||||||
Medical condition: Epithelial Ovarian Cancer | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) AT (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-024111-13 | Sponsor Protocol Number: AIO-STO-0110 | Start Date*: 2011-04-15 | |||||||||||||||||||||
Sponsor Name:AIO-Studien-gGmbH | |||||||||||||||||||||||
Full Title: Explorative trial to investigate catumaxomab (anti-EpCAM x anti-CD3) for treatment of peritoneal carcinomatosis in patients with gastric adenocarcinomas prior to gastrectomy | |||||||||||||||||||||||
Medical condition: Gastric adenocarcinoma and carcinoma of the esophago-gastric junction (type II and type III according to Siewert’s classification) prior to gastrectomy, with peritoneal carcinomatosis. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) | |||||||||||||||||||||||
Trial results: View results |
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: 2009-015082-31 | Sponsor Protocol Number: M10-757 | Start Date*: 2010-04-07 | |||||||||||
Sponsor Name:Abbott GmbH & Co. KG | |||||||||||||
Full Title: A Phase 2 Randomized Clinical Trial of ABT-888 in Combination with Temozolomide Versus Pegylated Liposomal Doxorubicin Alone in Subjects with Recurrent High Grade Serous Ovarian Cancer | |||||||||||||
Medical condition: Recurrent high grade serous ovarian cancer. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: HU (Completed) GB (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 |
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