Status:
COMPLETED
A Phase II Study to Treat Subjects With Advanced Renal Cell Carcinoma
Lead Sponsor:
Amgen
Conditions:
Advanced Renal Cell Carcinoma
Eligibility:
All Genders
18+ years
Phase:
PHASE2
Brief Summary
The purpose of this study is to evaluate the effectiveness and safety of AMG 102 in patients with Advanced Renal Cancer.
Eligibility Criteria
Inclusion
- documented histologically confirmed advanced or metastatic renal cell carcinoma with the primary tumor in place or following nephrectomy
- measurable disease, defined as ≥ 1 unidimensionally measurable lesion ≥ 20 mm by conventional techniques (CT or MRI) or ≥ 10 mm by spiral CT scan
- no more than 3 relapses (or prior systemic treatments)
- unable to receive or failed prior therapy with vascular endothelial growth factor (VEGF) binding agents or VEGF receptor tyrosine kinase inhibitors or other multi-kinase inhibitors
- tissue blocks or tissue sections from initial or upon diagnosis of advanced metastatic disease are available for submission to the central laboratory within approximately 4 weeks after enrollment or approval is granted by the sponsor (upon receipt of justification why the sample is not available)
- age ≥ 18 years
- ECOG performance status of 0-2
- hemoglobin concentration ≥ 9 g/dL
- absolute neutrophil count ≥ 1.5 x 10(9th)/L
- corrected serum calcium ≤ 10 mg/dL
- either serum creatinine \< 2.0 x upper limit of normal OR creatinine clearance \> 40 mL/min
- alanine aminotransferase ≤ 2.5 times upper limit of normal or \< 5.0 x ULN if the subject has documented liver metastasis or primary hepatic neoplasm
- serum total bilirubin ≤ 2.5 times upper limit of normal
- before any study-specific procedure, the appropriate written informed consent must be obtained
Exclusion
- active brain metastases; brain metastases allowed provided they have been treated with surgery and/or radiation therapy and show no evidence of progression on cerebral CT or MRI scan 2 months following surgery and/or radiation therapy
- concurrent severe and/or uncontrolled medical disease (e.g., uncontrolled diabetes, congestive cardiac failure, myocardial infarction within 6 months before enrollment) that could compromise participation in the study
- documented history of human immunodeficiency virus infection
- documented history of viral chronic hepatitis
- received biologic, small molecule, immunotherapy, chemotherapy, radiotherapy or other agents to treat renal cancer within 28 days before enrollment
- treated previously with c-Met or HGF targeted therapy
- concurrent or prior (within 7 days before enrollment) anticoagulation therapy, except:
- Use of low-dose warfarin (\< 2 mg/day) for prophylaxis against central venous catheter thrombosis or
- Use of low molecular weight heparins (LMWH, e.g., enoxaparin sodium \[Lovenox\] and unfractionated heparin for prophylaxis against central venous catheter thrombosis is allowed
- concurrent use of hormones or other chemotherapeutic agents except for steroids given for adrenal failure and hormones administered for non-disease-related conditions (eg, insulin for diabetes); except for non-cancer reasons
- concurrent palliative or therapeutic radiation therapy
- currently enrolled in or has not yet completed at least 30 days since ending other investigational device or therapy, or subject is receiving other investigational agent(s)
- active infection requiring treatment within 1 week before enrollment
- undergone major surgery within 4 weeks before enrollment or recovering from prior surgery
- past or current history of another neoplasm, except for curatively treated non-melanoma skin cancer, carcinoma in situ of the cervix and other primary solid cancer with no known active disease present and no curative treatment administered for the last 3 years
- known allergy or sensitivity to any of the excipients in the investigational product to be administered
- pregnant or is breast feeding
- not consenting to use adequate contraceptive precautions during the course of the study and for 6 months after the last administration of investigational product:
- female subjects who are not post-menopausal (no menstrual period for a minimum of 12 months at study entry) or documented surgically sterile will not be bound to this exclusion
- previously treated with AMG 102
- previously enrolled into this study
- will not be available for follow-up assessments
- has other disorders that compromises the ability of the subject to give written informed consent and/or comply with study procedures
- unable to begin protocol specified treatment within 3 days after enrollment
Key Trial Info
Start Date :
January 1 2007
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 1 2009
Estimated Enrollment :
61 Patients enrolled
Trial Details
Trial ID
NCT00422019
Start Date
January 1 2007
End Date
March 1 2009
Last Update
April 10 2015
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