Panitumumab in Children With Solid Tumors

Completed · Phase 1

Conditions studied: Solid Tumors

In brief

The primary objective of this study was to evaluate the safety and pharmacokinetics of up to 3 different dose schedules of panitumumab in pediatric patients with solid tumors.

Key facts

Study ID

NCT00658658

Run by

Amgen

People needed

31

Starts

2008-03-01

Expected to finish

2015-03-01

Last updated by the study team

2016-05-18

Who can join

Age: 1 and older, up to 17. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Parents or legal guardian signed-written informed consent
• 1 to < 18 years of age
• Histologically or cytologically confirmed solid tumor that has recurred after standard therapy, or for which there is no standard therapy. Subjects with brainstem glioma DO NOT need histologic proof of the diagnosis.
• Paraffin-embedded tumor tissue from primary tumor or metastasis for determination of epidermal growth factor receptor expression and biomarker testing
• Central nervous system tumors are allowed
• Presence of measurable or non-measurable disease.
• Life expectancy of ≥ 12 weeks.
• Performance status: Karnofsky ≥ 60% for 12 to <18 years of age; Lansky play scale ≥ 60% for 1 to < 12 years of age.
• Adequate hematologic function.
• Adequate renal function.
• Adequate hepatic function.
• Magnesium ≥ lower limit of normal (LLN)
• Adequate pulmonary function
• All previous therapy-related toxicities must have resolved or return to baseline.

You may not qualify if…

• Diagnosis of leukemia, non-Hodgkin's lymphoma, Hodgkin's disease or other hematologic malignancy.
• Any prior allogeneic transplant.
• Prior autologous bone marrow or peripheral stem cell transplant less than 3 months prior to enrollment.
• Substantial radiotherapy to the bone marrow within 6 weeks prior to enrollment.
• Prior use of any monoclonal antibodies directly targeting the epidermal growth factor receptor (EGFr). Subjects who have received prior tyrosine kinase inhibitors such as gefitinib or erlotinib are eligible.
• Immunotherapy, radiotherapy, or chemotherapy ≤ 2 weeks prior to enrollment. (≤ 6 weeks for nitrosoureas, mitomycin-C, and liposomal doxorubicin, and ≤ 6 weeks from prior antibody therapy).
• Requirement to receive concurrent chemotherapy, immunotherapy, radiotherapy (except for pain control) or any other investigational drug while on this study.
• Prior seizures < 3 months prior to enrollment. Subjects with a history of seizure disorders ≥ 3 months prior to enrollment must be seizure free and on stable anticonvulsant medication(s) for ≥ 3 months prior to enrollment).
• Presence of a serious uncontrolled medical disorder.
• Dementia, altered mental status, or any other medical condition or disorder that would prohibit the understanding or rendering of assent (if applicable), or ability to comply with study procedures.
• Major surgery ≤ 28 days prior to enrollment.
• Known or suspected history of interstitial lung disease.
• Active inflammatory bowel disease or other bowel disease causing chronic diarrhea.
• Known positive test for human immunodeficiency virus infection, hepatitis C virus, acute or chronic hepatitis B infection, or any co-morbid disease that would increase risk of toxicity.
• Females of childbearing potential not using adequate contraception precautions for the duration of the study treatment and for 2 months after the last administration of investigational product.
• Pregnant or breast-feeding, or planning to become pregnant during study treatment and within 2 months after the last administration of investigational product.
• Received investigational therapy or procedure ≤ 30 days prior to enrollment.

Where it is running

• Research Site — Los Angeles, California, United States
• Research Site — San Francisco, California, United States
• Research Site — Washington D.C., District of Columbia, United States
• Research Site — Chicago, Illinois, United States
• Research Site — Minneapolis, Minnesota, United States
• Research Site — Kansas City, Missouri, United States
• Research Site — New York, New York, United States
• Research Site — Cleveland, Ohio, United States
• Research Site — Portland, Oregon, United States
• Research Site — Nashville, Tennessee, United States
• Research Site — Houston, Texas, United States

Full record on ClinicalTrials.gov

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