Study of IMC-11F8 in Patients With Tumors Who Have Not Responded to Standard Therapy

PHASE1CompletedINTERVENTIONAL
Enrollment

60

Participants

Timeline

Start Date

November 30, 2004

Primary Completion Date

February 28, 2007

Study Completion Date

February 28, 2007

Conditions
Solid Tumors
Interventions
BIOLOGICAL

IMC-11F8

"Cohort 1~100 mg I.V."

BIOLOGICAL

IMC-11F8

"Cohort 2~200 mg I.V."

BIOLOGICAL

IMC-11F8

"Cohort 3~400 mg I.V."

BIOLOGICAL

IMC-11F8 I.V.

"Cohort 4~600 mg I.V."

BIOLOGICAL

IMC-11F8

"Cohort 5~800 mg I.V."

BIOLOGICAL

IMC-11F8

"Cohort 6~1000 mg I.V."

BIOLOGICAL

IMC-11F8

"Cohort 1~100 mg I.V."

BIOLOGICAL

IMC-11F8

"Cohort 2~200 mg I.V."

BIOLOGICAL

IMC-11F8

"Cohort 3~400 mg I.V."

BIOLOGICAL

IMC-11F8

"Cohort 4~600 mg I.V."

BIOLOGICAL

IMC-11F8

"Cohort 5~800 mg I.V."

BIOLOGICAL

IMC-11F8

"Cohort 6~1000 mg I.V."

Trial Locations (2)

1081 HV

ImClone Investigational Site, Amsterdam

3508 GA

ImClone Investigational Site, Utrecht

All Listed Sponsors
lead

Eli Lilly and Company

INDUSTRY

NCT00801177 - Study of IMC-11F8 in Patients With Tumors Who Have Not Responded to Standard Therapy | Biotech Hunter | Biotech Hunter