Pancreatic, gastric, and colorectal cancers have all been shown to overexpress the gastrin gene and to be sensitive to the trophic effects of the gastrin in animal models. The hypothesis of this study is that G17DT will elicit specific and high-affinity antibodies that will bind gastrin-17, thus preventing the trophic activity of cancer cells.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
11
University Hospital, Queen's Medical Centre
Nottingham, Nottinghamshire, United Kingdom
Number of participants with adverse effects
Time frame: Up to week 16
Measure serum anti gastrin-17 antibodies to determine immunological response to medication
Time frame: Up to week 16
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