Study of PHA-848125AC in Adult Patients With Advanced/Metastatic Solid Tumors

Exclusion Criteria

• •In the past 6 months: myocardial infarction, unstable angina, coronary/peripheral artery bypass graft, symptomatic congestive heart failure, cerebrovascular accident or transient ischemic attack, pulmonary embolism, deep vein thrombosis
• •Known brain metastases
• •Major surgery, other than diagnostic surgery, within 4 weeks prior to Day 1
• •Active, uncontrolled bacterial, viral, or fungal infections, requiring systemic therapy
• •Pregnant or breast feeding women
• •Unwillingness or inability to comply with procedures required in this protocol
• •Known infection with HIV, active hepatitis B or hepatitis C
• •Diabetes mellitus uncontrolled, or with clinical evidence of diabetic retinopathy, severe peripheral vascular disease or diabetic ulcers
• •Current enrollment in another clinical trial
• •Patients who have exhibited allergic reactions to a similar structural compound, biological agent, or formulation (lactose intolerance)
• •Previous history or current presence of neurological disorders, including epilepsy (although controlled by anticonvulsant therapy), Parkinson's disease, multiple sclerosis, stroke and cerebellar injury
• •Gastrointestinal disease (e.g. Crohn's disease, ulcerative colitis, or short gut syndrome) that would impact on drug absorption
• •Chronic/intensive use of antacid or H2 receptor antagonists
• •Other severe acute or chronic medical or psychiatric condition or laboratory abnormality that may increase the risk associated with study participation or may interfere with the interpretation of study results and, in the judgment of the investigator, would make the patient inappropriate for entry into this study or could compromise protocol objectives in the opinion of the investigator and/or the sponsor.