This is an open-label phase 1-b study to evaluate the safety and efficacy of CCX872-B in patients with pancreatic adenocarcinoma also receiving FOLFIRINOX chemotherapy.
Study acquired by Amgen and all disclosures were done by previous sponsor ChemoCentryx.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
54
Tablets (oral administration)
Unnamed facility
St Louis, Missouri, United States
Unnamed facility
Rochester, New York, United States
Unnamed facility
Amsterdam, Netherlands
Unnamed facility
Nijmegen, Netherlands
Netherland
progression-free survival
Time frame: 24 weeks
subject incidence of Grade 3 or 4 adverse events
Time frame: 24 weeks
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Rotterdam, Netherlands
Unnamed facility
Sittard, Netherlands