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 @ 9:14 PM
Ignite Modification Date:
2025-12-24 @ 9:14 PM
NCT ID:
NCT01170104
Eligibility Criteria:
Inclusion Criteria:
1. Unresectable Hepatocellular carcinoma with local liver lesion treatable with TACE
2. Age \> 18 years.
3. ECOG Performance Status of 0 or 1.
4. Child-Pugh class A (class B could be included when Childs score is 7).
5. Life expectancy of at least 12 weeks.
6. Subjects with at least one measurable lesion.
7. Adequate bone marrow, liver and renal function as assessed by the following laboratory requirements to be conducted within 7 days prior to screening:
* Hemoglobin \> 9.0 g/dl
* Absolute neutrophil count (ANC) \>1,500/mm3
* Platelet count \> 75,000/μl
* Total bilirubin \< 1.5 times the upper limit of normal
* ALT and AST \< 2.5 x upper limit of normal (UNL)
* Alkaline phosphatase \< 5 x ULN
* PT-INR/PTT \< 1.5 x upper limit of normal
* Serum creatinine \< 1.5 x ULN
8. Signed and dated informed consent before the start of specific protocol procedures
Exclusion Criteria:
1. History of cardiac disease: congestive heart failure \>NYHA class 2; active CAD (MI more than 6 mo prior to study entry is allowed); cardiac arrythmias requiring anti-arrythmic therapy( beta blockers or digoxin are permitted) or uncontrolled hypertension.
2. History of HIV infection.
3. Active clinically serious infections (\> grade 2 NCI-CTC version 3.0)
4. Symptomatic metastatic brain or meningeal tumors (unless the patient is \> 6 months from definitive therapy, has a negative imaging study within 4 weeks of study entry and is clinically stable with respect to the tumor at the time of study entry)
5. Patients with seizure disorder requiring medication (such as steroids or anti-epileptics)
6. History of organ allograft The organ allograft may be allowed as protocol specific.
7. Patients with evidence or history of uncontrolled bleeding diathesis
8. Patients undergoing renal dialysis
9. Previous or concurrent cancer that is distinct in primary site or histology from the cancer being evaluated in this study EXCEPT cervical carcinoma in situ, treated basal cell carcinoma, superficial bladder tumors \[Ta, Tis \& T1\] or any cancer curatively treated \> 3 years prior to study entry.
10. Excluded therapies and medications, previous and concomitant:
* Anticancer chemotherapy or immunotherapy during the study or within 4 weeks of study entry
* Radiotherapy during study or within 3 weeks of start of study drug. (Palliative radiotherapy will be allowed). Major surgery within 4 weeks of start of study
* Investigational drug therapy outside of this trial during or within 4 weeks of study entry
* Prior exposure to the study drug.
* Pregnant or breast-feeding patients. Women of childbearing potential must have a negative pregnancy test performed within 7 days of the start of treatment. Both men and women enrolled in this trial must use adequate barrier birth control measures during the course of the trial (and men for at least 3 months after last administration of study medication).
* Substance abuse, medical, psychological or social conditions that may interfere with the patient's participation in the study or evaluation of the study results
* Any condition that is unstable or could jeopardize the safety of the patient and their compliance in the study
* Patients unable to swallow oral medications
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT01170104
Study Brief:
Protocol Section:
NCT01170104