Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 2:34 AM
Ignite Modification Date:
2025-12-25 @ 2:34 AM
NCT ID:
NCT02089334
Eligibility Criteria:
Inclusion Criteria:
* Males and females ≥ 18 years of age at screening
* Histological or cytological diagnosis of renal cell cancer with a clear-cell component
* Measurable or evaluable disease defined by Response Evaluation Criteria for Solid Tumors (RECIST) ver. 1.1
* Must have received at least one course of therapy with a VEGFR-targeting tyrosine kinase inhibitor (eg, sorafenib, sunitinib, axitinib, pazopanib or tivozanib) and progressed within 6 months of planned first dose of study treatment
* ECOG performance status of 0,1 or 2
* Life expectancy \> 3 months
* Provide written informed consent
Exclusion Criteria:
* Brain metastases or cranial epidural disease unless adequately treated with radiotherapy and/or surgery and stable for at least 3 months before planned first dose of study drug
* Radiation therapy for bone metastasis within 2 weeks, any other external radiation therapy within 4 weeks before planned first dose of study drug. Systemic treatment with radionuclides within 6 weeks before planned first dose of study drug. Subjects with clinically relevant ongoing complications from prior radiation therapy are not eligible
* Prior treatment with everolimus, or any other specific or selective TORC1/PI3K/AKT inhibitor (eg, temsirolimus)
* Receipt of any type of small molecule kinase inhibitor (including investigational kinase inhibitor) within 2 weeks before planned first dose of study drug
* Receipt of any type of anticancer antibody (including investigational antibody) within 4 weeks before planned first dose of study drug
* Taking strong inducers or inhibitors of CYP450s for subjects receiving everolimus
* Chronic treatment with corticosteroids or other immunosuppressive agents
* Concomitant anticoagulation at therapeutic doses with oral anticoagulants or platelet inhibitors
* Subjects with a known hypersensitivity to everolimus or other rapamycins (sirolimus, temsirolimus) or to its excipients
* Major surgery within 2 months before planned first dose of study drug
* Myocardial infarction within the previous 6 months before planned first dose of study drug
* Active infection requiring parenteral antibiotics within 2 weeks before planned first dose of study drug
* Diagnosis of another malignancy within 2 years before planned first dose of study drug, except for superficial skin cancers, or localized, low grade tumors
* Prior or current history of hepatitis B, hepatitis C or human immunodeficiency virus
* Sexually active fertile subjects (male and female) must agree to use medically accepted methods of contraception during the course of the study and for 30 days after the last dose of study treatment
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT02089334
Study Brief:
Protocol Section:
NCT02089334