Feasibility of the LUM Imaging System for Peritoneal Surface Malignancies

Exclusion Criteria

• •Subjects who are pregnant or nursing at the time of diagnosis.
• •Subjects who are sexually active and not willing/able to use medically acceptable forms of contraception (hormonal or barrier method of birth control, abstinence) upon entering the study and for 60 days after injection of LUM015.
• •Subjects who have taken an investigational drug within 30 days of enrollment.
• •Subjects who have not recovered from adverse events due to other pharmaceutical or diagnostic agents.
• •Subjects with uncontrolled hypertension defined as persistent systolic blood pressure \> 180 mm Hg, or diastolic blood pressure \> 100 mm Hg; those subjects with known HTN should be under these values while under pharmaceutical therapy.
• •History of allergic reaction attributed to drugs containing polyethylene glycol (PEG).
• •History of allergic reaction to any oral or intravenous contrast agents.
• •Uncontrolled intercurrent illness including, but not limited to ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, COPD or asthma requiring hospitalization within the past 12 months, or psychiatric illness/social situations that would limit compliance with study requirements.
• •HIV-positive individuals on combination antiretroviral therapy are ineligible.
• •Any subject for whom the investigator feels participation is not in the best interest of the subject.