Safety Study of XL999 in Adults With Non-Small-Cell Lung Cancer

Exclusion Criteria

• •1. The subject has received systemic anticancer therapy (eg, chemotherapy, biologic therapy, targeted therapy, cytokines, or hormones) within 14 days before the first dose of study drug.
• •2. The subject has received radiation to \>25% of his or her bone marrow within 30 days of XL999 treatment.
• •3. The subject has not recovered to Grade ≤1 from adverse events (AEs) due to investigational or other agents administered more than 14 days prior to study enrollment.
• •4. The subject has history of or known brain metastases, current spinal cord compression, or carcinomatous meningitis.
• •5. The subject is known to be positive for the human immunodeficiency virus (HIV).
• •6. The subject has uncontrolled and/or intercurrent illness including but not limited to the following:
• •1. Cardiac:
• •* Left ventricular ejection fraction (LVEF) assessed by 99mTc multiple-gated acquisition scan (MUGA) is below the institution's lower limit of normal (LLN) at screening. If regional wall motion abnormalities are noted on the MUGA, cardiology consultation should be performed prior to enrollment.
• •* History of pulmonary hypertension.
• •* History of congestive heart failure (CHF) (New York Heart Association \[NYHA\] Class II, III, or IV).
• •* Active or unstable ischemic disease, including angina pectoris, myocardial infarction, coronary artery bypass grafting (CABG) within the past 12 months.
• •* Electrocardiogram (ECG) showing signs of ischemia or myocardial, valvular, or coronary artery disease unless deemed clinically insignificant by a cardiologist.
• •* Onset of any changes between the screening ECG and pre-dose ECG unless deemed clinically insignificant by a cardiologist.
• •* ECG abnormalities that could cause interpretation difficulties after XL999 administration (eg, left bundle branch block \[LBBB\], atrial fibrillation, A-V blocks, pacemakers, digoxin).
• •2. Vascular:
• •* Blood pressure \>150/90 mm Hg despite antihypertensive therapy with two medications.
• •* Cerebrovascular accident, transient ischemic attack, or evidence of active peripheral vascular disease within 12 months prior to study enrollment.
• •3. Hematologic:
• •* National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) v3.0 Grade ≥3 hemorrhage within 30 days of study enrollment.
• •* Evidence of bleeding diathesis or coagulopathy.
• •* Requirement for therapeutic anticoagulation. Patients receiving anticoagulants (eg, warfarin, heparin) will be excluded if international normalized ratio \>1.5 or partial thromboplastin time (PTT) \>1.5× the institution's ULN.
• •4. Recent surgical procedures:
• •* Major surgery or open biopsy within 30 days of starting treatment with XL999.
• •* Anticipation of major surgical procedure during the study.
• •5. Wound healing problems:
• •* History of abdominal fistula, gastrointestinal perforation, or intra-abdominal abscess within 30 days prior to treatment.
• •* Serious, non-healing wound, ulcer, or bone fracture.
• •6. Psychiatric illness that would limit compliance with study requirements.
• •7. The subject is pregnant or breastfeeding.
• •8. The subject has a known allergy or hypersensitivity to components of the XL999 formulation.
• •9. The subject is unable or unwilling to abide by the study.