A Study of BBI608 and BBI503 Administered in Combination to Adult Patients With Advanced Solid Tumors

PHASE1CompletedINTERVENTIONAL
Enrollment

147

Participants

Timeline

Start Date

April 30, 2015

Primary Completion Date

December 31, 2019

Study Completion Date

April 30, 2020

Conditions
CancerAdvanced Solid Tumors
Interventions
DRUG

BBI608

The BBI608 starting dose is 240 mg twice daily (480 mg total daily). Dose will be decreased to 160 mg twice daily (320 mg total daily) at modification level 2 and 80 mg twice daily (160 mg total daily) at modification level 3. For BBI608 once daily dosing, doses at starting level and modification level 1 are 240 mg once daily, and 480 mg once daily at escalated levels. Dose will be decreased to 160 mg once daily at modification level 2 and 80 mg once daily at modification level 3.

DRUG

BBI503

The BBI503 starting dose is 200 mg once daily. Dose at modification level 1 to 3 will be 100 mg once daily.

Trial Locations (11)

10065

Weill Cornell Medical College, New York

22031

Virginia Cancer Specialists, PC, Fairfax

46202

Indiana University Simon Cancer Center, Indianapolis

60637

University of Chicago Medicine Comprehensive Cancer Center, Chicago

75246

Texas Oncology - Baylor Charles A. Sammons Cancer Center, Dallas

75702

Texas Oncology - Tyler, Tyler

76104

Texas Oncology - Austin Midtown, Austin

Texas Oncology - Fort Worth 12th Ave, Fort Worth

78217

Texas Oncology, P.A., San Antonio

78229

Texas Oncology, P.A., San Antonio

98684

Northwest Cancer Specialists, PC, Vancouver

All Listed Sponsors
lead

Sumitomo Pharma America, Inc.

INDUSTRY

NCT02432326 - A Study of BBI608 and BBI503 Administered in Combination to Adult Patients With Advanced Solid Tumors | Biotech Hunter | Biotech Hunter