Study Of Bosutinib With Capecitabine In Solid Tumors And Locally Advanced Or Metastatic Breast Cancer

PHASE1/PHASE2TerminatedINTERVENTIONAL
Enrollment

32

Participants

Timeline

Start Date

September 30, 2009

Primary Completion Date

March 31, 2011

Study Completion Date

March 31, 2011

Conditions
Advanced Breast Cancer (Parts 1 and 2)Advanced Pancreatic Cancer (Part 1)Advanced Colorectal Cancer (Part 1)Advanced Cholangiocarcinoma (Part 1)Advanced Glioblastoma Multiforme (Part 1)
Interventions
DRUG

Bosutinib

Doses in part 1 include bosutinib 200 mg QD; bosutinib 300 mg QD. Depending on safety bosutinib can be administered at 200 mg/m2 QD. The MTD of the combination treatment determined from part 1, will be administered in part 2 (phase 2).

DRUG

Capecitabine

Doses in part 1 include capecitabine 750 mg/m2 BID on days 1-14; capecitabine 625 mg/m2 BID on days 1-14. Depending on safety, capecitabine can also be administered at 1000 mg/m2 BID. The MTD of the combination treatment determined from part 1, will be administered in part 2 (phase 2).

Trial Locations (7)

2650

Pfizer Investigational Site, Edegem

5037

Pfizer Investigational Site, Adelaide

28050

Pfizer Investigational Site, Madrid

44805

Pfizer Investigational Site, Saint-Herblain

84202

Pfizer Investigational Site, Detroit

02114

Pfizer Investigational Site, Boston

Unknown

Pfizer Investigational Site, Hong Kong

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Pfizer

INDUSTRY