Know Cancer

forgot password

A Single Arm Phase II Study of the Efficacy, Safety, and Biomarkers of Activity of E7820 Plus Cetuximab in Advanced Solid Tumors Preceded by a Run-In Study to Determine Safety of the Combination

Phase 2
18 Years
Not Enrolling
Advanced Colorectal Cancer

Thank you

Trial Information

A Single Arm Phase II Study of the Efficacy, Safety, and Biomarkers of Activity of E7820 Plus Cetuximab in Advanced Solid Tumors Preceded by a Run-In Study to Determine Safety of the Combination

Inclusion Criteria:

- For Phase Ib, patients must have a histologically or cytologically confirmed
malignant solid tumor for which no effective therapy is available or the patient must
not be a candidate for standard therapy.

- For Phase II, patients must have a pathologically and histologically documented
colorectal carcinoma that is inoperable and/or metastatic. These patients must also
have at least one unidimensional measurable lesion according to the RECIST

- Patients must have an ECOG Performance Status of 0-1.

- Patients must have a life expectancy of >= 3 months.

- Patients must be aged >= 18 years.

- Patients must have adequate renal function as evidenced by serum creatinine < 2 mg/dL
and creatinine clearance > 40 mL/minute.

- Patients must have adequate bone marrow function as evidenced by ANC >= 1,500 /mm3
and platelets >= 100,000 /mm3.

- Patients must have adequate hepatic function as evidenced by liver function test
abnormalities no greater than CTC grade 1 (bilirubin, alanine transaminase [ALT], and
aspartate transaminase [AST]) unless increased LFTs are related to liver metastases
in which case CTC grade 2 abnormalities acceptable.

- Patients must be willing and able to comply with the study protocol for the duration
of the study.

- Patients must give written informed consent prior to any study-specific screening
procedures with the understanding that the patient may withdraw consent at any time
without prejudice.

- Patients may have received prior bevacizumab therapy as long as therapy has been
discontinued for 4 weeks or longer.

Exclusion Criteria:

- Patients who have a history of previous Grade 2 or higher hypersensitivity to
sulfonamide derivatives.

- Patients previously treated with cetuximab, or who have received prior treatment with
any EGFR-related cancer therapy, either an approved or investigational agent.

- Patients with known sensitivity to murine monoclonal antibodies.

- Patients who have had radiation to >= 25% of their bone marrow (e.g., pelvic
radiation) within 4 weeks prior to E7820 treatment.

- Patients who have not recovered from any clinically significant (Grade 3 or 4)
chemotherapy, immunotherapy, or radiotherapy related toxicity at study entry
(excluding neuropathy, infertility, or alopecia).

- Patients who have received investigational drugs or any other anti-neoplastic therapy
within 28 days of E7820 treatment.

- Patients who have had major surgery within 4 weeks of study drug administration.

- Women who are pregnant or breast-feeding. Women of childbearing potential with
either a positive pregnancy test at screening or no pregnancy test. Women of
childbearing potential unless using adequate measures of contraception in the opinion
of the Investigator (postmenopausal women must be amenorrheic for at least 12 months
to be considered of non-childbearing potential).

- Fertile men and fertile women who are not willing to use contraception or fertile men
or fertile women with a partner who is not willing to use contraception.

- Patients with brain or subdural metastases are not eligible except if they have
completed local therapy and have discontinued the use of corticosteroids for this
indication for at least one month before starting treatment with E7820. Any signs
(eg, radiologic) and/or symptoms from their brain metastases must be stable for at
least one month.

- Patients who have a positive history of human immunodeficiency virus, hepatitis B or
active hepatitis C.

- Patients with severe uncontrolled intercurrent illness/infection (excluding

- Patients with a history of unstable ischemic cardiac disease or more than Class II
NYHA heart failure.

- Patients with a history of clinically significant arterial thrombosis or who have
taken therapeutic doses of anticoagulants within the last 7 days.

- Patients who have pulmonary disease that puts them at risk of hemoptysis or bleeding
diathesis. Head and neck cancer patients at risk for major vessel bleeding.

- Patients receiving therapeutics doses of anticoagulants.

- Patients with poorly controlled type I insulin-dependent diabetes or
poorly-controlled type II insulin-dependent diabetes or a fasting blood glucose >10
mmol/L (200 mg/dL).

- Patients with significant comorbid disease or condition, which in the Investigator's
opinion would exclude the patient from the study.

Type of Study:


Study Design:

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Outcome Measure:

Objective tumor response (CR or PR) and disease control (CR, PR or SD) rates will be evaluated in this study based on RECIST criteria and modified WHO criteria.

Outcome Time Frame:

The timing will be based on RECIST criteria and modified WHO criteria.

Safety Issue:


Principal Investigator

Eisai Medical Services

Investigator Role:

Study Director

Investigator Affiliation:

Eisai Inc.


United States: Food and Drug Administration

Study ID:




Start Date:

August 2006

Completion Date:

Related Keywords:

  • Advanced Colorectal Cancer
  • Advanced colorectal cancer
  • Colorectal Neoplasms



Fountain Valley, California  92708
Miami, Florida  33176