A Study of IMC-A12 in Participants With Tumors Who No Longer Respond to Treatment or For Whom No Treatment is Available

PHASE1CompletedINTERVENTIONAL
Enrollment

24

Participants

Timeline

Start Date

October 31, 2005

Primary Completion Date

January 31, 2011

Study Completion Date

January 31, 2011

Conditions
Advanced Solid Tumors
Interventions
BIOLOGICAL

IMC-A12

"Cohort 1~3 milligrams/kilogram (mg/kg), I.V. once a week, for 4 weeks, followed by a 2-week observation period."

BIOLOGICAL

IMC-A12

"Cohort 2~6 mg/kg, I.V. once a week, for 4 weeks, followed by a 2-week observation period."

BIOLOGICAL

IMC-A12

"Cohort 3~10 mg/kg, I.V. once a week, for 4 weeks, followed by a 2-week observation period."

BIOLOGICAL

IMC-A12

"Cohort 4~15 mg/kg, I.V. once a week, for 4 weeks, followed by a 2-week observation period."

BIOLOGICAL

IMC-A12

"Cohort 5~21 mg/kg, I.V. once a week, for 4 weeks, followed by a 2-week observation period."

BIOLOGICAL

IMC-A12

"Cohort 6~27 mg/kg, I.V. once a week, for 4 weeks, followed by a 2-week observation period."

Trial Locations (3)

48201

ImClone Investigational Site, Detroit

85258

ImClone Investigational Site, Scottsdale

98109

ImClone Investigational Site, Seattle

All Listed Sponsors
lead

Eli Lilly and Company

INDUSTRY

NCT00785538 - A Study of IMC-A12 in Participants With Tumors Who No Longer Respond to Treatment or For Whom No Treatment is Available | Biotech Hunter | Biotech Hunter