Evaluating E7389 in Patients With Hormone Refractory Prostate Cancer With Advanced and/or Metastatic Disease Stratified by Prior Chemotherapy

PHASE2CompletedINTERVENTIONAL
Enrollment

108

Participants

Timeline

Start Date

January 31, 2006

Primary Completion Date

January 31, 2008

Study Completion Date

January 31, 2008

Conditions
Prostate Cancer
Interventions
DRUG

E7389

Intravenous 1.4 mg/m2 on a 3-week course.

Trial Locations (18)

10019

St. Luke's Roosevelt Hospital Center, New York

10032

Columbia University Medical Center, New York

12208

New York Oncology Hematology, P.C., Albany

23505

Virginia Oncology Associates, Norfolk

27607

Raleigh Hematology Oncology Associates PL, Raleigh

32901

Melbourne Internal Medicine Associates, Melbourne

33557

Minnesota Hematology Oncology, Burnsville

34474

Ocala Oncology Center PL, Ocala

46227

Central Indiana Cancer Centers, Indianapolis

65201

Missouri Cancer Associates, Columbia

75204

US Oncology, Dallas

75246

Mary Crowley Medical Research Center, Dallas

75702

Texas Oncology PA, Tyler

Tyler Cancer Center, Tyler

76104

Texas Oncology PA, Fort Worth

77598

Deke Slayton Cancer Center, Webster

79915

El Paso Cancer Treatment Center, El Paso

80218

Dr. Robert Jotte, Denver

All Listed Sponsors
lead

Eisai Inc.

INDUSTRY

NCT00278993 - Evaluating E7389 in Patients With Hormone Refractory Prostate Cancer With Advanced and/or Metastatic Disease Stratified by Prior Chemotherapy | Biotech Hunter | Biotech Hunter