Pancreatic Cancer Clinical Trial
Official title:
An Open-Label Phase 2 Study of AGS-1C4D4 in Pancreatic Cancer Subjects Previously Treated in Protocol 2008002
The purpose of this study is to continue the safety and immunogenicity of AGS-1C4D4 administered in combination with gemcitabine in subjects previously treated in protocol 2008002.
Subjects will receive a maintenance dose of AGS-1C4D4 every 3 weeks (Q3W) in addition to the
gemcitabine administration. If subjects have grade 4 adverse events considered to be related
to AGS-1C4D4 at anytime during the study, AGS-1C4D4 treatment will be discontinued for that
subject.
Subjects will continue to have their tumor status assessed by computerized tomography (CT)
and magnetic resonance (MRI) scans according to Response Evaluation Criteria in Solid Tumors
(RECIST Version 1.1) guidelines every eight weeks (Q8W). Subjects without evidence of
disease progression will continue to receive AGS-1C4D4 and gemcitabine until intolerability,
disease progression or consent withdrawal.
Subjects who discontinue AGS-1C4D4 for any reason will undergo an end of study visit 4 weeks
after their last AGS-1C4D4 infusion.
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