Efficacy and Safety Study of Imprime PGG With Cetuximab in Subjects With Stage IV KRAS-Mutated Colorectal Cancer

CompletedOBSERVATIONAL
Enrollment

18

Participants

Timeline

Start Date

June 30, 2009

Primary Completion Date

February 29, 2012

Study Completion Date

February 29, 2012

Conditions
Colorectal Cancer
Interventions
BIOLOGICAL

Imprime PGG

Imprime PGG, 4 mg/kg, i.v. over 2 hr, weekly in 6 week cycles and Cetuximab, initial dose will be 400 mg/m2 via i.v., and subsequent doses will be 250 mg/m2 via i.v., weekly in 6 week cycles

Trial Locations (3)

Unknown

University of Minnesota, Minneapolis

Memorial Sloane-Kettering Cancer Research Center, New York

Mary Crowley Medical Research Center, Dallas

Sponsors

Lead Sponsor

All Listed Sponsors
lead

HiberCell, Inc.

INDUSTRY

NCT00912327 - Efficacy and Safety Study of Imprime PGG With Cetuximab in Subjects With Stage IV KRAS-Mutated Colorectal Cancer | Biotech Hunter | Biotech Hunter