Clinical Study of Ixabepilone Administered as a 24 Hour Infusion in Patients With Solid Malignancies.

PHASE1CompletedINTERVENTIONAL
Enrollment

35

Participants

Timeline

Start Date

September 30, 2005

Primary Completion Date

July 31, 2008

Study Completion Date

July 31, 2008

Conditions
Solid Malignancies
Interventions
DRUG

Ixabepilone

Intravenous (IV) Infusion; 10, 20, 30, 35, 40 \& 45 mg/m2, once every 21 days (1 cycle), up to 9 cycles

Trial Locations (3)

21201

University Of Maryland, Baltimore

44195

Cleveland Clinic Foundation, Cleveland

08901

The Cancer Institute Of New Jersey, New Brunswick

Sponsors

Lead Sponsor

All Listed Sponsors
lead

R-Pharm

INDUSTRY

NCT00162136 - Clinical Study of Ixabepilone Administered as a 24 Hour Infusion in Patients With Solid Malignancies. | Biotech Hunter | Biotech Hunter