E7389
Sponsors
Eisai Inc., Eisai Co., Ltd.
Conditions
Advanced Solid TumorsBladder CancerBreast CancerBreast NeoplasmsCancerProstate CancerSoft Tissue SarcomaUnspecified Adult Solid Tumor, Protocol Specific
Phase 1
Study of E7389 in Patients With Advanced Solid Tumors
CompletedNCT00069264
Start: 2003-09-30End: 2005-07-31Updated: 2011-12-20
Study of E7389 Administered Once Every 3 Weeks In Patients With Advanced Solid Tumors
CompletedNCT00069277
Start: 2003-08-31End: 2005-04-30Updated: 2012-04-11
Phase I Clinical Study of E7389
CompletedNCT00326950
Start: 2006-06-30End: 2008-02-29Updated: 2012-03-08
Study Of Eribulin (E7389) In Patients With Advanced Solid Tumors And Normal Or Reduced Hepatic Function As Per Child-Pugh System
CompletedNCT00706095
Start: 2008-02-29End: 2010-04-30Updated: 2012-03-27
Eribulin Mesylate Administered in Combination With Gemcitabine Plus Cisplatin Versus Gemcitabine Plus Cisplatin Alone as First-Line Therapy for Locally Advanced or Metastatic Bladder Cancer
TerminatedNCT01126749
Start: 2010-04-16End: 2016-07-20Updated: 2022-02-28
An Open-Label Study to Assess the Pharmacokinetics and Safety of HALAVEN in Subjects With Cancer Who Also Have Impaired Renal Function
CompletedNCT01418677
Start: 2011-10-31End: 2015-05-31Updated: 2016-05-17
A Study of Eribulin Mesylate With Trastuzumab for Advanced or Recurrent Human Epidermal Growth Factor Receptor 2-Positive (HER2+) Breast Cancer
CompletedNCT01432886
Start: 2011-10-31End: 2013-12-31Updated: 2016-10-07
Phase 2
A Study of E7389 in Advanced/Metastatic Breast Cancer Patients
CompletedNCT00097721
Start: 2004-09-30End: 2006-11-30Updated: 2013-04-22
A Phase II Study of E7389 in Patients With Breast Cancer, Previously Treated With Anthracycline, Taxane and Capecitabine
CompletedNCT00246090
Start: 2005-10-31End: 2007-09-30Updated: 2014-07-14
Evaluating E7389 in Patients With Hormone Refractory Prostate Cancer With Advanced and/or Metastatic Disease Stratified by Prior Chemotherapy
CompletedNCT00278993
Start: 2006-01-31End: 2008-01-31Updated: 2014-07-14
E7389 Administered as an IV Bolus Infusion Day 1 and Day 8 Every 3 Weeks in Pre-Treated Patients With Advanced and/or Metastatic Soft Tissue Sarcoma
CompletedNCT00413192
Start: 2007-01-31End: 2013-02-28Updated: 2017-04-26