Study Of SU011248 In Combination With Paclitaxel In Patients With Metastatic Breast Cancer

PHASE1CompletedINTERVENTIONAL
Enrollment

22

Participants

Timeline

Start Date

September 30, 2005

Primary Completion Date

August 31, 2007

Study Completion Date

August 31, 2007

Conditions
Breast Neoplasms
Interventions
DRUG

SU011248

SU011248 provided as capsules. The starting dose is 25 mg orally, daily in a continuous regimen beginning on day 2. Dose rest for 1 week is allowed. Dose escalation to 37.5 mg po OD is allowed within the constraints of acceptable toxicity parameters. Dosing will continue for 1 year or until disease progression or unacceptable toxicity, whichever comes first.

DRUG

Paclitaxel

Paclitaxel is provided as an intravenous infusion for 1 hour weekly for 3 weeks followed by a 1-week rest. The starting dose is 90 mg/m2. The weekly dose may be decreased to 65 mg/m2 in subsequent cycles based on tolerability. Dosing will continue for 1 year or until maximum benefit, disease progression or unacceptable toxicity, whichever comes first.

Trial Locations (6)

10021

Pfizer Investigational Site, New York

46202

Pfizer Investigational Site, Indianapolis

46290

Pfizer Investigational Site, Indianapolis

46321

Pfizer Investigational Site, Munster

60426

Pfizer Investigational Site, Harvey

60426-4265

Pfizer Investigational Site, Harvey

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Pfizer

INDUSTRY

NCT00174434 - Study Of SU011248 In Combination With Paclitaxel In Patients With Metastatic Breast Cancer | Biotech Hunter | Biotech Hunter