Safety and Efficacy Study of BMS-908662 Alone or in Combination With Cetuximab in Subjects With K-RAS or B-RAF Mutation Positive Advanced or Metastatic Colorectal Cancer

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

17

Participants

Timeline

Start Date

July 31, 2010

Primary Completion Date

August 31, 2011

Study Completion Date

August 31, 2011

Conditions
Colorectal Cancer
Interventions
DRUG

BMS-908662

Capsules, Oral, escalating doses starting at 25 mg, every 12 hours (Q 12 h), Continuously

DRUG

BMS-908662

Capsules, Oral, (TBD) mg, Q 12 h, Continuously

DRUG

Cetuximab

Vial, IV, 400 mg/m² loading dose followed by 250 mg/m² maintenance dose, Weekly, Continuously

Trial Locations (3)

85258

Oncology Research Associates D/B/A, Scottsdale

90033

Usc Norris Comprehensive Cancer Center, Los Angeles

K1H 1C3

Local Institution, Ottawa

Sponsors
All Listed Sponsors
lead

Bristol-Myers Squibb

INDUSTRY