Safety Study of TAK-700 in Subjects With Prostate Cancer.

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

123

Participants

Timeline

Start Date

April 30, 2008

Primary Completion Date

January 31, 2013

Study Completion Date

February 28, 2013

Conditions
Prostatic Neoplasms
Interventions
DRUG

TAK-700

"Phase 1 portion of study:~TAK-700 dose escalation. Tablets administered orally, twice daily until disease progression or occurrence of an unacceptable adverse event.~Phase 2 portion of study:~Patients will receive one of 4 treatments:~* TAK-700 at 300 mg twice/day~* TAK-700 at 400 mg and 5 mg prednisone twice/day~* TAK-700 at 600 mg and 5 mg prednisone twice/day~* TAK-700 at 600 mg once/day in the morning"

Trial Locations (19)

44195

Cleveland Clinic, Cleveland

60611

Northwestern University Medical Center, Chicago

60637

University of Chicago, Chicago

90048

University of Southern California, Los Angeles

Unknown

USC Westside Prostate Cancer Center, Beverly Hills

The Angeles Clinic and Research Institute, Los Angeles

USC Norris Comprehensive Cancer Center, Los Angeles

South Florida Medical Research, Aventura

Florida Cancer Specialists, Fort Myers

University of Chicago Comprehensive Cancer Center, Chicago

University of Chicago Pharmacy, Chicago

Evanston Hospital, Evanston

Kellogg Pharmacy - Evanston Hospital, Evanston

NorthShore University HealthSystem, Evanston

Kellogg Cancer Care Center, Glenview

Hematology/Oncology Associates of Central New York, East Syracuse

Gabrail Cancer Center, Canton

Taussig Cancer Institute, Cleveland

Tennessee Oncology, Nashville

All Listed Sponsors
lead

Millennium Pharmaceuticals, Inc.

INDUSTRY

NCT00569153 - Safety Study of TAK-700 in Subjects With Prostate Cancer. | Biotech Hunter | Biotech Hunter