A Study of Ramucirumab or Icrucumab in Colorectal Cancer

Completed · Phase 2

Conditions studied: Colon Cancer, Rectal Cancer

In brief

The purpose of this study is to determine if participants with metastatic colorectal cancer live longer without their cancer progressing when treated with standard chemotherapy, standard chemotherapy plus ramucirumab, or standard chemotherapy plus icrucumab.

Key facts

Study ID

NCT01111604

Run by

Eli Lilly and Company

People needed

158

Starts

2010-08-01

Expected to finish

2013-12-01

Last updated by the study team

2019-08-06

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Disease progression on an irinotecan-based first-line chemotherapy regimen (ie FOLFIRI or CAPIRI [capecitabine + irinotecan], with or without bevacizumab)
• Age ≥ 18 years
• Life expectancy of ≥ 6 months
• Eastern Cooperative Oncology Group Performance Status (ECOG PS) 0-1 at study entry
• Agrees to adequate contraception during the study period and for 12 weeks after the last dose of study medication
• Provided signed informed consent

You may not qualify if…

• Has received prior oxaliplatin-based chemotherapy for locally advanced unresectable or metastatic Colorectal Cancer (CRC) (Prior oxaliplatin-based adjuvant chemotherapy is allowed if the last dose of oxaliplatin was administered > 12 months prior to randomization)
• Has documented and/or symptomatic brain or leptomeningeal metastases
• Has an ongoing or active infection, symptomatic or poorly controlled cardiac arrhythmia, psychiatric illness/social situations, or any other serious uncontrolled medical disorders
• On chronic non-topical corticosteroid treatment. A participant discontinuing such treatment > 3 months prior to randomization is eligible
• Has uncontrolled or poorly controlled hypertension on a standard regimen of antihypertensive therapy
• Has a concurrent active malignancy. A participant with previous history of malignancy is eligible, provided that he/she has been disease free for > 3 years
• If female, is pregnant (confirmed by serum beta human chorionic gonadotropin [βHCG] test) or lactating
• Has received a prior autologous or allogeneic organ or tissue transplantation
• Has undergone major surgery within 28 days prior to randomization
• Has had a serious nonhealing wound, ulcer, or bone fracture within 28 days prior to randomization
• Has an elective or planned major surgery to be performed during the course of the trial
• Has a history of inflammatory bowel disease requiring pharmacological and/or surgical intervention in the 12 months prior to randomization

Where it is running

• ImClone Investigational Site — Cincinnati, Ohio, United States
• ImClone Investigational Site — Columbia, South Carolina, United States
• ImClone Investigational Site — Nashville, Tennessee, United States
• ImClone Investigational Site — Calgary, Alberta, Canada
• ImClone Investigational Site — Edmonton, Alberta, Canada
• ImClone Investigational Site — Kelowna, British Columbia, Canada
• ImClone Investigational Site — Surrey, British Columbia, Canada
• ImClone Investigational Site — Vancouver, British Columbia, Canada
• ImClone Investigational Site — Halifax, Nova Scotia, Canada
• ImClone Investigational Site — Hamilton, Ontario, Canada
• ImClone Investigational Site — London, Ontario, Canada
• ImClone Investigational Site — Mississauga, Ontario, Canada
• ImClone Investigational Site — Oshawa, Ontario, Canada
• ImClone Investigational Site — Ottawa, Ontario, Canada
• ImClone Investigational Site — Toronto, Ontario, Canada
• ImClone Investigational Site — Windsor, Ontario, Canada
• ImClone Investigational Site — Montreal, Quebec, Canada

Full record on ClinicalTrials.gov

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