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 @ 1:21 PM
Ignite Modification Date:
2025-12-24 @ 1:21 PM
NCT ID:
NCT00830895
Eligibility Criteria:
Inclusion Criteria:
1. Histologically or cytologically confirmed non-clear cell renal cell carcinoma (papillary, chromophobe, collecting duct, oncocytic subtype, sarcomatoid mainly)
2. Subjects with metastatic legion
3. Subjects aged 18 years or older
4. Subjects whose ECOG performance status is 0 or 1
5. Subjects who have laboratory value below; Hematology
* Neutrophil \>= 1.5 x 109/L
* Platelet \>= 75 x 109/L
* Hemoglobin \>= 9 g/dL Liver function tests
* Total bilirubin ≤ 1.5 xULN
* AST, ALT ≤ 2.5 xULN
* Alkaline phosphatase ≤ 2.5 xULN Renal function tests
* Creatinine clearance \>= 30 mL/min
6. Subjects who understand and provide a written informed consent
Exclusion Criteria:
1. Subjects who have been administered an mTOR inhibitor
2. Pregnant or nursing women, and women of childbearing potential must use appropriate contraception for the study period and the result of their pregnancy test performed within 14 days before enrollment must be negative
3. Subjects who participated in a clinical study using the study medication within 30 days before randomization
4. Subjects with clinically uncontrolled central nervous system (CNS) metastasis
5. Subjects with life expectancy of less than 3 months
6. Subjects with interstitial pulmonary disease
7. Subjects whose QTc interval is prolonged (QTc \> 450 msec for male or \> 470 msec for female)
8. Other serious diseases or medical conditions Heart disease unstable despite treatment History of myocardial infarction within six months before the study History of serious neurological or psychological disorder including dementia or seizure Active peptic ulcer which cannot be controlled by a drug
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT00830895
Study Brief:
Protocol Section:
NCT00830895