A Study of EZN-2208 Administered With or Without Cetuximab in Patients With Metastatic Colorectal Carcinoma

Status unconfirmed · Phase 2

Conditions studied: Metastatic Colorectal Cancer

In brief

This is a Phase 2, multicenter, multiple-arm, open-label study to evaluate the efficacy, safety, and tolerability of EZN-2208. EZN-2208 will be administered as a single agent in patients with K-RAS mutations in the tumors. Patients with wild type K-RAS in tumors will be randomized to EZN-2208 + cetuximab or to standard of care (Camptosar® + cetuximab), patients must have failed regimens containing irinotecan (Camptosar®, CPT-11), oxaliplatin (Eloxatin®), and fluoropyrimidine. After discontinuation of study treatment, patients will receive care as considered appropriate by the investigator. Patients will continue to be followed for disease progression, subsequent anticancer therapy, and survival.

Key facts

Study ID

NCT00931840

Run by

Enzon Pharmaceuticals, Inc.

People needed

220

Starts

2009-06-01

Expected to finish

2012-01-01

Last updated by the study team

2011-09-20

Who can join

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

You may qualify if…

• Patients must meet all of the following criteria to be eligible for enrollment in the study.
• Histologically confirmed CRC adenocarcinoma that is metastatic or locally recurrent CRC that is nonresectable
• Patients must agree to genetic testing of the original or metastatic CRC tumor biopsy tissue for K-RAS mutational status.
• Disease progression
• Previous therapy with irinotecan, oxaliplatin, and fluoropyrimidine either alone or in any combination(s). Patients must have radiographically documented progressive disease while receiving, or within 3 months of receiving, these agents alone or in combination.
• No more than 2 prior cytotoxic chemotherapy regimens.
• Age 18 years or older
• Measurable disease by RECIST Version 1.1
• ECOG performance status of 0 or 1
• Adequate bone marrow, renal, and hepatic function

You may not qualify if…

• Patients meeting any of the following exclusion criteria will not be eligible for enrollment.
• Known chronic infectious disease
• Major surgery within 3 weeks before study start
• Known or suspected brain metastases requiring intervention with steroids and/or radiation therapy.
• Prior chemotherapy, immunotherapy, non-investigational agent, or other therapy used to treat the cancer within 3 weeks before the scheduled administration of EZN-2208
• History of other primary cancer within 5 years of enrollment, unless
• Curatively resected non-melanomatous skin cancer, or
• Curatively resected cervical cancer
• Lack of recovery to Grade 1 from any reversible side effects related to the administration of an investigational agent, or other prior treatments for the cancer
• Any condition such as uncontrollable diabetes, uncontrollable hypertension, or active infection.
• Current participation in another clinical study with an investigational agent and/or use of an investigational drug (not including investigational use of an approved drug) in the 30 days before the first administration of EZN-2208

Where it is running

• Location# 074 — Montreal, Quebec, Canada
• Location# 055 — Rimouski, Quebec, Canada
• Location# 066 — Tel-Aviv, Central District, Israel
• Location# 071 — Kfar Saba, Sharon, Israel
• Location# 072 — Beersheba, South District, Israel
• Location# 068 — Be’er Ya‘aqov, Israel
• Location# 067 — Haifa, Israel
• Location# 073 — Jerusalem District, Israel
• Location# 070 — Tel Aviv, Israel
• Location# 069 — Tel Litwinsky, Israel
• Location# 041 — Leiden, NL, Netherlands
• Location # 040 — Rotterdam, The Netherlands, Netherlands
• Location #065 — Dorchester, Dorset, United Kingdom
• Location # 083 — London, England, United Kingdom
• Location# 057 — London, Greater London, United Kingdom
• Location# 054-2 — London, Greater London, United Kingdom
• Location #061 — London, Greater London, United Kingdom
• Location# 064 — Manchester, Greater Manchester, United Kingdom
• Location# 056 — Edinburgh, Scotland, United Kingdom
• Location# 062 — Glasgow, Scotland, United Kingdom
• Location# 054 — Sutton, Surrey, United Kingdom
• Location# 063 — Leeds, West Yorkshire, United Kingdom
• Location #033 — Tucson, Arizona, United States
• Location# 042 — Alhambra, California, United States
• Location# 077 — Montreal, Quebec, Canada

Full record on ClinicalTrials.gov

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