Safety Study of SGX523, a Small Molecule Met Inhibitor, to Treat Solid Tumors

• Subject has the ability to understand, able, willing to comply with study procedures and follow up visits, and has provided written consent.
• Pathologic evidence of solid tumor.
• Failed standard therapy and deemed by the Investigator to be suitable for participation into the trial.
• Laboratory values (obtained within 10 days prior to enrollment): ANC: >= 1.5 × 109/L; Platelets: >= 100 × 109/L; Hemoglobin: >= 10.0 g/dL (without transfusions); Bilirubin: within normal range; AST, ALT, and alkaline phosphatase: \<= 2.5 x ULN without tumor liver involvement; Serum creatinine: within normal limits; Calculated creatinine clearance: >= 60 mL/min/1.73 m2 for patients with creatinine > Institutional Normal Values; PT/PTT/INR: within normal limits.
• Have IHC evidence of phospho-MET expression on tumor material no more than 12 months old. This is a requirement only for entry into the MTD dose expansion phase.
• Have no residual toxic effects of previous therapy, and undergo a washout period of at least 5 half-lives from the time of administration of the previous therapy.

Exclusion Criteria:

• Pregnant, lactating, or may become pregnant.
• Cardiac disease requiring medical therapy.
• Have had a major surgery within 4 weeks prior to Day 1 of the study
• Have an active, uncontrolled bacterial, viral, or fungal infection that requires ongoing systemic therapy.
• Have a known active infection with HIV, hepatitis B or C.
• Have psychiatric or seizure disorders that would require therapy or interfere with study participation.
• Have other severe concurrent nonmalignant disease that could compromise protocol objectives, including malabsorptive conditions.
• Patients receiving prohibited medications as listed in Appendix E, including drugs categorized as strong inhibitors of CYP3A4 and A5 and drugs known to have a high potential risk of liver toxicity.
• Have known allergy to SGX523 formulation or its excipients (croscarmellose sodium, lactose monohydrate and magnesium stereate).
• Patients receiving anti-coagulant therapy.