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 @ 1:33 PM
Ignite Modification Date:
2025-12-24 @ 1:33 PM
NCT ID:
NCT01055795
Eligibility Criteria:
Inclusion Criteria:
1. Histologically and/or cytologically confirmed malignant solid tumor that is refractory to standard therapies, or for which no standard therapies exist.
2. Patients must have at least one measurable site of disease according to RECIST (see Appendix 1) criteria that has not been previously irradiated. If the patient has had previous radiation to the marker lesion(s), there must be evidence of progression since the radiation
3. Age ≥ 18 years
4. Karnofsky Performance status ≥ 80% (see Appendix 2)
5. Adequate bone marrow function as shown by:
1. ANC ≥ 1.5 x 109/L
2. Platelets ≥ 100 x 109/L
3. Hemoglobin \>9 g/dL; Erythropoietin and transfusion support is permitted provided treatments are not required more than every 8 weeks.
6. Adequate liver function as shown by:
1. serum bilirubin ≤ 1.5 x ULN
2. INR ≤ 1.5
3. ALT and AST ≤ 2.5x ULN (≤ 5x ULN in patients with liver metastases)
7. Adequate renal function: creatinine clearance (estimated) ≥ 40 cc/min
8. Fasting serum cholesterol ≤ 300 mg/dL OR ≤ 7.75 mmol/L AND fasting triglycerides ≤ 2.5 x ULN. NOTE: Use of standard lipid lowering agents (see Section 10.3.6 for guidance) is permitted to meet eligibility.
9. Fasting blood sugar \<160 mg/dL.
10. Baseline MUGA or ECHO must demonstrate LVEF ≥ 50%
11. TSH and free T4 within normal limits; Patients are permitted to receive thyroid hormone supplements to treat underlying hypothyroidism.
12. Women of childbearing potential (WOCBP) must have a negative serum pregnancy test within 7 days from day 1 of study drug and must be willing to use two methods of contraception, one of them being a barrier method during the study and for 3 months after last study drug administration
13. Signed informed consent
Exclusion Criteria:
1. Patients currently receiving anticancer therapies or who have received anticancer therapies within 4 weeks from day 1 of study drug (including chemotherapy, radiation therapy, antibody based therapy, etc.)
2. Patients who:
1. have had a major surgery or significant traumatic injury within 4 weeks from day 1 of study drug,
2. have not recovered from the side effects of any major surgery (defined as requiring general anesthesia) or
3. are anticipated to require major surgery during the course of the study.
3. Patients with a known hypersensitivity to experimental drugs (or classes of drugs) or their excipients
4. Patients receiving chronic, systemic treatment with corticosteroids or another immunosuppressive agent with the following exceptions:
* Intermittent steroids ( not to exceed 4 mg every day) may be used on an as-needed basis (e.g. treatment for chemotherapy-related nausea.)
* Patients on physiologic replacement doses of steroids due to adrenal insufficiency for any reason may remain on these medications.
* Topical, inhaled or intra-articular corticosteroids
5. Patients should not receive immunization with attenuated live vaccines within one week of day 1 of study drug or during study period
6. Active brain or leptomeningeal metastases, including patients who continue to require glucocorticoids for brain or leptomeningeal metastases. Treated, asymptomatic metastases are permitted provided the patient has been off steroids for at least 1 month prior to day 1 of study drug.
7. Clinically significant arrhythmias including complete left bundle branch block or use of a permanent cardiac pacemaker, congenital long QT syndrome, history or presence of ventricular tachyarrhythmias, 2nd degree AV block type II, 3rd degree AV block clinically significant resting bradycardia (\<50 beats per minute), QTcF \> 450 msec on screening ECG.
8. Presence of poorly controlled atrial fibrillation (ventricular heart rate \>100 bpm)
9. Previous history of CVA, TIA, angina pectoris, acute MI or history of recent re-perfusion procedures (e.g. PTCA) within 6 months from day 1 of study drug.
10. Congestive heart failure (New York Heart Association (NYHA classification, see Appendix 4 functional classification III-IV).
11. Fasting blood sugar \> 160 mg/dL despite standard of supportive care. Patients may start or adjust anti-diabetic medications to meet eligibility.
12. Patients who have any severe and/or uncontrolled medical conditions or other conditions that could affect their participation in the study as so judged by the treating physician. Examples include but are not limited to:
1. Severely impaired lung function (e.g. use of home O2, history of Idiopathic Lung Disease (ILD), any evidence of ILD on scan.
2. Active (acute or chronic) or uncontrolled severe infections requiring treatment with antibiotics
3. Liver disease such as cirrhosis, chronic active hepatitis or chronic persistent hepatitis
4. Uncontrolled hypertension, BP\>150/100 despite medical management
5. Impairment of gastrointestinal function or gastrointestinal disease that may significantly alter the absorption of oral medications (e.g., ulcerative disease, uncontrolled nausea, vomiting, diarrhea, malabsorption syndrome or small bowel resection)
13. Significant vascular disease (e.g., aortic aneurysm requiring surgical repair or recent peripheral arterial thrombosis) within 6 months prior to day 1 of study drug
14. History of hemoptysis (\>/= 1/2 teaspoon of bright red blood per episode) within 1 month prior to day 1 of study drug
15. History of abdominal fistula or gastrointestinal perforation at any point within 6 months prior to day 1 of study drug, unless surgically repaired.
16. Use or need for full dose anticoagulation other than low molecular weight heparin (i.e. Lovenox only with and no other bleeding risk)..
17. Invasion or encasement of a major artery. Abutment without invasion or encasement is permitted. Abutment is defined as loss of the tissue plane between tumor and vessel but without invasion of the soft tissues or lumen of the vessel. Encasement is defined as more than 180 degrees of involvement
18. Serious, non-healing wound, active ulcer, or untreated bone fracture as judged by treating physician
19. Active, bleeding diathesis
20. Known history of HIV or Hepatitis B or C seropositivity
21. Female patients who are pregnant or breast feeding, or adults of reproductive potential who are not using effective birth control methods. Two acceptable forms of contraceptives must be continued throughout the trial by both sexes. Hormonal contraceptives are not acceptable as a sole method of contraception. (Women of childbearing potential must have a negative serum pregnancy test within 7 days prior to day 1 of study drug)
22. Concomitant use of drugs with a risk of causing torsades de pointes (See Appendix 5 )
23. Concomitant use of CYP3A4 inhibitors (See Appendix 6)
24. Patients unwilling to or unable to comply with the protocol
25. Intrathoracic lung carcinoma of squamous cell histology. Mixed tumors will be categorized by the predominant cell type unless small cell elements are present, in which case the patient is ineligible; sputum cytology alone is acceptable. Patients with extrathoracic-only squamous cell NSCLC are eligible. Patients with only peripheral lung lesions (of any NSCLC histology) will also be eligible (a peripheral lesion is defined as a lesion in which the epicenter of the tumor is \</= 2 cm from the costal or diaphragmatic pleura in a three-dimensional orientation based on each lobe of the lung and is \</= 2 cm from the trachea, main, and lobar bronchi).
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
90 Years
Study:
NCT01055795
Study Brief:
Protocol Section:
NCT01055795