Study of IMC-11F8 in Patients With Tumors Who Have Not Responded to Standard Therapy

Lilly

Status and phase

Completed

Phase 1

Conditions

Solid Tumors

Treatments

Biological: IMC-11F8

Biological: IMC-11F8 I.V.

Study type

Interventional

Funder types

Industry

Identifiers

NCT00801177

CP11-0401 (Other Identifier)

2004-002072-42 (EudraCT Number)

14088

Details and patient eligibility

About

The purpose of this study is to determine if IMC-11F8 is safe for patients, and also to determine the best dose of IMC-11F8 to give to patients.

Full description

The purpose of this study is to establish the safety profile and the maximum tolerated dose (MTD) of the fully human anti-EGFR monoclonal antibody IMC-11F8 in patients with solid tumors who have filed standard therapy or for whom no standard therapy is available.

Enrollment

60 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Histologically-confirmed, EGFR-detectable or EGFR-undetectable, unidimensionally-measurable and/or evaluable solid tumors who failed standard therapy or for whom no standard therapy is available. Patients who do not have tissue available for EGFR testing will undergo a biopsy of an accessible tumor.
ECOG performance status score of ≤ 2 at study entry.
Able to provide written informed consent.
White blood cell (WBC) count ≥ 3 x 109/L; an absolute neutrophil count ≥ 1.5 x 109/L; a hemoglobin level > 90 g/L; and a platelet count ≥ 100 x 109/L.
Adequate hepatic function as defined by:
- an alkaline phosphatase level ≤ 5.0 x the ULN
- a bilirubin level ≤ 1.5 x the ULN
- aspartate transaminase (AST) and alanine transaminase (ALT) levels ≤ 2.5 x the ULN or ≤ 5 x the ULN for patients with liver metastases
Adequate renal function as defined by a serum creatinine level within normal limits.
Use of effective contraception if procreative potential exists.
Life expectancy of approximately 3 months in the opinion the opinion of the investigator.

Exclusion criteria

Chemotherapy, radiation, and/or hormonal therapy (except palliative radiation therapy for disease-related pain and chronic hormonal therapy for prostate carcinoma) within 4 weeks of study entry.
Concurrent unstable or uncontrolled medical disease (e.g., active uncontrolled systemic infection, poorly controlled hypertension or history of poor compliance with an anti-hypertensive regimen, unstable angina, congestive heart failure, uncontrolled diabetes) or other chronic disease, which, in the opinion of the investigator, could compromise the patient or the study.
Newly-diagnosed or symptomatic brain metastases (patients with a history of brain metastases must have received definitive surgery or radiotherapy, be clinically stable, and not taking steroids; anticonvulsants are allowed).
Any concurrent malignancy other than basal cell carcinoma or carcinoma in situ of the cervix. Patients with a previous malignancy but without evidence of disease for ≥ 3 years will be allowed to enter the trial.
Any condition that prevents the patient from providing informed consent.
Pregnancy (confirmed by serum beta human chorionic gonadotropin [ßHCG]) or breast-feeding.
Any investigational agent(s) or device(s) within 4 weeks of study entry.
Prior treatment with cetuximab, or any other epidermal growth factor receptor inhibitors, including tyrosine kinase inhibitors, such as gefitinib or erlotinib. Prior treatment with other monoclonal antibodies targeting receptors other than the EGFR is permitted ≥ 4 weeks prior to study entry.
Any prior therapy that targeted the EGFR or EGFR pathway.
Known history of human immunodeficiency virus.
Employees of the investigator or study center with direct involvement in this study or other studies under the direction of the investigator or study center, as well as family members of the employees.