Sequential Trial of G17DT for the Treatment of Advanced Pancreatic Cancer

You may not be if

• Male or female subjects over 18 years of age
• Subjects with a life expectancy of at least 2 months
• KPS score of ≥60%
• Written informed consent
• Previous, concomitant, or anticipated use (up to Week 12) of chemotherapy, radiotherapy, immunotherapy, or any other anticancer therapy
• Previous (during the 4 weeks before the study), concomitant, or anticipated use (up to Week 12) of immunosuppressants. However, for systemic \[i.e., oral or injected\] corticosteroids, previous use and concomitant use at study entry were prohibited, while introduction during the course of the study was permitted.)
• History of other malignant tumor within the previous 5 years, except nonmelanomatous skin cancer, and in situ carcinoma of the uterine cervix
• Known immunodeficiency
• Females who were pregnant, planning to become pregnant, or lactating (Women who, in the opinion of the investigator, were of childbearing potential were to have a negative pregnancy test before study drug administration.)
• Subjects taking part in another study involving an investigational or licensed drug or device in the 3 months preceding enrollment or up to Week 12 during this study
• Previous G17DT treatment
• Hematological indicators as follows:
• * Hemoglobin \<9.5 g/dL
• * Neutrophils \<2.0 × 109/L
• * Platelets \<100 × 109/L
• Any other condition or circumstance that might have the following results:
• * Worsen if the subject participated in the study
• * Reduce the subject's ability to comply with the protocol
• * Confound the interpretation of the study results