All clinical trials on the European Union Clinical Trials Register (EUCTR) must report their results in the registry within a year of completion. This site tracks who's doing this and who isn't. Learn more »
These trials completed more than 12 months ago and should have reported results. Some have, some have not.
These trials are not yet due to report results: some are ongoing, some completed within the past 12 months.
These trials have problematic data on the registry. Details why »
Status | Trial ID | Title | Completion date | Category |
---|---|---|---|---|
Not reported | 2004-000232-91 | EICH Profilaxis con ATeGe-FRESENIUS en trasplante alogénico de progenitores hematopoyéticos procedente de donantes no emparentados | 2015-02-26 | due-trials |
Not reported | 2004-000723-15 | 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 x ... | 2006-11-02 | due-trials |
Completed, but no date | 2004-001349-14 | A Study Extension to Evaluate the Safety and Tolerability of Liposome Entrapped Paclitaxel Easy to Use (LEP-ETU) in Patients that Completed Study LEP-ETU-102A | bad-data | |
Not reported | 2005-001131-30 | A Double-Blind, Placebo-Controlled, Multicenter, Dose-ranging Study of an Anti-T-lymphocyte Immunglobuline (EZ-2053) in the Prophylaxis of Acute Pulmonary Allograft Rejection in Adult Recipients of Pr... | 2011-01-25 | due-trials |
Not reported | 2005-001700-39 | Determination of systemic exposure and characterization of pharmacokinetics of the tri-functional antibody catumaxomab (anti-EpCAM X anti-CD3) administered intraperitoneally in EpCAM positive cancer p... | 2006-11-07 | due-trials |
Not reported | 2005-004294-21 | Estudio de fase II del anticuerpo trifuncional anti-HER-2/neu x anti-CD3 ertumaxomab en pacientes con cáncer de mama avanzado o metastásico resistente al tratamiento hormonal que expresa HER2/neu 1+ ... | 2009-02-03 | due-trials |
Not reported | 2005-004431-21 | Estudio abierto, multicéntrico, aleatorio, con el objetivo de evaluar la eficacia y la seguridad de la inmunosupresión tras un primer trasplante renal cadavérico a corazón latiente basado la utilizaci... | 2010-04-29 | due-trials |
Not reported | 2005-005945-20 | 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 resection ... | 2009-06-22 | due-trials |
Not reported | 2006-002727-16 | 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 after n... | 2013-04-26 | due-trials |
Not reported | 2006-004484-54 | 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 | 2008-08-08 | due-trials |
Listed as ongoing, but also has a completion date | 2006-005017-36 | Phase II Study for repeated dosing of the trifunctional bispecific anti-HER-2/neu x anti-CD3 antibody ertumaxomab in patients with HER-2/neu 1+ or 2+/FISH negative expressing advanced or metastatic br... | 2009-02-03 | bad-data |
Exempt Terminated | 2006-006694-24 | Phase I/II dose-escalation study of the investigational trifunctional bispecific anti-CD20 x anti-CD3 antibody FBTA05 in relapsed or refractory chronic lymphocytic leukemia | 2009-02-03 | not-yet-due |
Completed, but no date Terminated | 2007-005261-35 | Treatment of Graves’ Orbitopathy (GO) with ATG-Fresenius: A prospective, randomized, open, controlled phase II study to assess the efficacy and safety of an add-on ATG-Fresenius treatment versus a sta... | bad-data | |
Listed as ongoing, but also has a completion date | 2008-001557-17 | 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 due t... | 2011-04-26 | bad-data |
Listed as ongoing, but also has a completion date | 2009-014076-22 | 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 tr... | 2011-05-10 | bad-data |