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:
2025-12-24 @ 10:06 PM
Ignite Modification Date:
2025-12-24 @ 10:06 PM
NCT ID:
NCT01715935
Eligibility Criteria:
Inclusion Criteria:
* Advanced RCC or a resectable renal tumor and at least one measurable inoperable metastasis (at least 1 cm), in whom anti-angiogenic therapy is indicated
* Patients without target lesions, with bone metastasis
* Histologically confirmed clear cells RCC and possibility of adequate tumor sampling prior to treatment
* No prior systemic treatment for RCC
* Male or female, at least 18 years
* PS ECOG 0-1
* Life expectancy at least 3 months
* Adequate organ function with the following criteria:
* Total serum bilirubin equal or less than 2 x ULN (Gilbert's disease exempted)
* Serum transaminases and alkaline phosphatases equal or less than 2.5 x ULN, or in case of liver or bone metastasis equal or less than 5x ULN
* Serum creatinine equal or less than 2 x ULN, creatinine clearance at least 50 ml/min
* Absolute neutrophil count (ANC) at least 1500/mm3
* Platelets at least 100,000/mm3
* Hemoglobin at least 10.0 g/dL
* INR equal or less than 1.7 or prothrombin time (PT) equal or less than 6 sec
* Blood glucose less than 1.5x ULN
* Fasting cholesterol equal or less than 5 mmol/L, triglycerides equal or less than 200 mg/dl,
* Negative pregnancy test within 7 days prior to enrollment
* Signed and dated IRB/ICE-approved informed consent form
* Willingness and ability to comply with scheduled visits, treatment plans, laboratory tests and other study procedures.
* Patient covered by the national health system
Exclusion Criteria:
* Previous nephrectomy
* Histology: any histologic type different than ccRCC
* Treatment in a clinical trial in the last 30 days
* Previous treatment with everolimus or other mTOR-inhibitors and anti-angiogenic drugs
* Any of the following within 12 months prior to treatment initiation: severe/unstable angina, myocardial infarction, coronary artery bypass graft, symptomatic congestive heart failure, ischemic or hemorrhagic stroke including transient ischemic attack, abnormal lung function.
* Uncontrolled hypertension defined as systolic blood pressure \>150 mmHg or diastolic pressure \>90 mmHg, despite optimal medical treatment
* Abnormal ECG (Clinically significant)
* Treatment with vitamin K antagonists. Ongoing treatment with therapeutic doses of coumarin derivative anticoagulants (e.g. warfarin) or treatment within the 2 weeks before the first day of everolimus administration. Prophylaxis with low dose warfarin for deep vein thrombosis is permitted (up to 2 mg/day). Low molecular weight heparin is allowed.
* Brain metastasis. (Brain scan or MRI is mandatory). Note: Previous treated brain metastasis (surgery ± radiotherapy, radiotherapy, radiosurgery or gammaknife) and satisfying the following three criteria are allowed:
* Asymptomatic;
* No evidence of any active brain metastasis 3 months prior inclusion;
* No necessity of corticoid or antiepileptic treatment.
* Pregnancy or breastfeeding.
* Any second malignancy within the last 3 years with the exception of basal cell carcinoma, in situ cervical cancer and pT1/a bladder cancer with no evidence of recurrent disease for 12 months.
* Clinically significant gastrointestinal abnormalities including but not limited to:
* Malabsorption syndrome
* Major resection of the stomach or small bowel that could affect the absorption of the study drug
* Active peptic ulcer disease
* Inflammatory bowel disease
* Ulcerative colitis or other gastrointestinal conditions with increased risk of perforation
* History of abdominal fistula, gastrointestinal perforation, or intra abdominal abscess within 28 days prior to beginning study treatment
* Hepatitis B/C
* Hypersensitivity to everolimus or any excipient of everolimus.
* Any active (acute or chronic) or uncontrolled infection/disorders that impair the ability to evaluate the patient or for the patient to complete the study.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT01715935
Study Brief:
Protocol Section:
NCT01715935