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COMPLETED

NCT02395068

PHASE1

Pharmacokinetics Study of Nimotuzumab in Patients With Solid Tumors

Sponsor: Biotech Pharmaceutical Co., Ltd.

View on ClinicalTrials.gov

Summary

Nimotuzumab is an IgG1 humanized monoclonal antibody that recognized an epitope located in the extra cellular domain of the human epidermal growth factor receptor (EGFR), inhibiting tyrosine kinase activation. It has been approved to treat squamous cell carcinoma of head and neck (SCCHN), glioma and nasopharyngeal carcinoma in different countries. Currently, the registered clinical trials of Nimotuzumab combined with chemotherapy in advanced non-small cell lung cancer, colorectal cancer, esophageal cancer and glioma have been approved and are ongoing all over the investigators' country. The main purpose of this study is to evaluate the pharmacokinetic characteristics of Nimotuzumab combined with Irinotecan in patients with solid tumors.

Official title: Pharmacokinetics Study of Nimotuzumab Single-dose and Multiple-dose in Combination With Irinotecan in Patients With Solid Tumors

Key Details

Gender

All

Age Range

18 Years - 70 Years

Study Type

INTERVENTIONAL

Enrollment

Start Date

2012-12

Completion Date

2014-10

Last Updated

2026-10-15

Healthy Volunteers

Conditions

Solid Tumors

Interventions

DRUG

Nimotuzumab

In period 1: Participants were administered single dose of nimotuzumab, via intravenous catheter (IV), with 3 weeks observation. In period 2: Participants were administered nimotuzumab (four dose levels: 100mg, 200mg, 400mg, 600mg) weekly, for 6 weeks.

DRUG

Irinotecan

In period 2: Participants were administered irinotecan (180mg/m\^2) biweekly, for 6 weeks.

Inclusion criteria: 1. Confirmed by pathology and / or cytology diagnosis in patients with advanced solid tumors 2. Failure of first-line or multi-line chemotherapy and be suitable for irinotecan therapy 3. Age 18-70 years, both genders at enrollment 4. ECOG 0 to 1 5. Adequate bone marrow function 6. Recover from the toxicity of previous treatment 7. At least one measurable site of disease as defined by at least 20mm in greatest dimension by CT or 10mm in greatest dimension by SCT/MRI 8. Male or female with fertility in the trial are willing to take contraceptive measures 9. Estimated life expectancy of 3 months or greater 10. All patients signed written informed consent Exclusion criteria: 1. Have previously received EGFR-targeted therapy 2. Current treatment on other effective programs 3. Participated in other clinical trial within 4 weeks after enrollment 4. Nervous system symptoms caused by brain metastases need to apply steroidal anti-edema medications to control 5. Persistent uncontrollable diarrhea CTCAE 2 level and above (4-6 times daily) 6. Complete or incomplete intestinal obstruction 7. Need to drainage pleural effusion and ascites 8. Drug addiction and other adverse long-term alcoholics, as well as AIDS patients 9. Occurred myocardial infarction within 6 months 10. Diagnosed with severe interstitial pneumonitis or pulmonary fibrosis by Chest CT 11. Severe or uncontrolled complications, such as infection required systemic treatment，fever（≥38℃），congestive heart failure，diabetes or hypertension that can not be controlled by drugs and other complications that may interfere with drug efficacy 12. Drug allergy（≥CTCAE 3.0）, such as shock or allergy symptoms, especially allergic to similar drugs in the past and severe hypersensitivity to polysorbate eighty-containing drugs 13. Uncontrollable seizures or loss of insight because of psychosis 14. Female patient is pregnant, breastfeeding, or of childbearing potential but not take contraceptive measures 15. Male patient who want his spouse to be pregnant during the trial 16. Researchers believe that should not participate in this trial

Locations (1)

Cancer Institute & Hospital, Chinese Academy of Medical Sciences

Beijing, Beijing Municipality, China