Study Evaluating SKI-606 (Bosutinib) In Advanced Malignant Solid Tumors

PHASE1CompletedINTERVENTIONAL
Enrollment

151

Participants

Timeline

Start Date

October 31, 2004

Primary Completion Date

November 30, 2007

Study Completion Date

November 30, 2007

Conditions
Neoplasms
Interventions
DRUG

bosutinib

Dose levels evaluated 50mg, 100mg, 200mg, 300mg, 400mg, 500mg and 600mg. 500mg was identified as MTD, however due to GI toxicities at that dose, 400mg was selected as the RP2D. Drug was administered as long as tolerable and disease under study did not worsen.

DRUG

bosutinib

400mg QD bosutinib, as long as tolerated and disease under study does not worsen.

DRUG

bosutinib

400mg QD bosutinib, as long as tolerated and disease under study does not worsen.

DRUG

bosutinib

400mg QD bosutinib, as long as tolerated and disease under study does not worsen.

Trial Locations (19)

10016

Pfizer Investigational Site, New York

10032

Pfizer Investigational Site, New York

21287

Pfizer Investigational Site, Baltimore

27514

Pfizer Investigational Site, UNC Chapel Hill

27759

Pfizer Investigational Site, UNC Chapel Hill

28203

Pfizer Investigational Site, Charlotte

28211

Pfizer Investigational Site, Charlotte

30341

Pfizer Investigational Site, Atlanta

33612

Pfizer Investigational Site, Tampa

35233

Pfizer Investigational Site, Birmington

46202

Pfizer Investigational Site, Indianpolis

48202

Pfizer Investigational Site, Detroit

48910

Pfizer Investigational Site, Lansing

75702

Pfizer Investigational Site, Tyler

78258

Pfizer Investigational Site, San Antonio

85258

Pfizer Investigational Site, Scottsdale

90033

Pfizer Investigational Site, Los Angeles

98104

Pfizer Investigational Site, Seattle

44106-1736

Pfizer Investigational Site, Cleveland

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Pfizer

INDUSTRY

NCT00195260 - Study Evaluating SKI-606 (Bosutinib) In Advanced Malignant Solid Tumors | Biotech Hunter | Biotech Hunter