test

E7208: A Randomized Phase II Study of Irinotecan and Cetuximab with or without the Anti-Angiogenic Antibody, Ramucirumab (IMC-1121B), in Advanced, K-ras Wild-type Colorectal Cancer Following Progression on Bevacizumab-Containing Chemotherapy

Conditions

Colon

What is the purpose of this trial?

- To evaluate the Progression Free Survival (PFS) for the addition of the anti-angiogenic antibody, Ramucirumab, in combination with irinotecan and cetuximab as second line therapy for patients with K-ras wild-type colorectal cancer, as compared to the patients without the antibody. - To evaluate the Response Rate for irinotecan, cetuximab and Ramucirumab in this patient population. - To evaluate the Grade 3-4 toxicity rates for the combination in this patient population. - To evaluate Overall Survival for irinotecan, cetuximab, and ramucirumab in this patient population.

Participation Guidelines

Age:
Gender:

Click here for detailed information about who can participate in this trial.


Sponsor:
Eastern Cooperative Oncology Group
Dates:
01/15/2011
Last Updated:
Study HIC#:
1010007561