This study was designed to investigate the safety and tolerance of three doses (100µg, 200µg, 500µg) of G17DT for the treatment of patients with colorectal cancer.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
5
Injection Site Reaction
An examination was performed to assess injection site tolerability at every posttreatment visit.
Time frame: Through Week 12
Antibody Levels
Gastrin-17 antibodies are produced as a result of treatment with G17DT and the proportion of patients producing gastrin-17 antibodies was considered to be an appropriate measure of the immunogenicity of the dosing schedule under study.
Time frame: Through Week 12
Intra-gastric pH
Compare the pre-immunization 24-hour intra-gastric pH with post-immunization profiles.
Time frame: Through Week 8
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