Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Arcus Biosciences, Inc.
With
Taiho Pharmaceutical Co., Ltd.
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Have histologically or cytologically confirmed PDAC that is metastatic.
Have not been previously treated for PDAC in the metastatic setting.
1. Prior neoadjuvant and/or adjuvant therapy for PDAC is permitted if completed at least 12 months before randomization.
2. Prior palliative radiotherapy is allowed if completed at least 2 weeks prior to randomization and AEs have resolved to Grade 1 or less before randomization.
3. Prior and/or placement of a biliary stent/tube is permitted if any treatment-related AEs have improved to Grade ≤ 1 and the patient is not exhibiting any signs/symptoms of biliary obstruction.
Eastern Cooperative Oncology Group PS of 0 to 1.
At least 1 target lesion measurable by computed tomography (CT)/magnetic resonance imaging (MRI) per RECIST v1.1. not within a field of prior radiation therapy.
You may not be if
Previously treated for locally advanced, unresectable PDAC.
History of brain metastases or leptomeningeal metastases.
Prior treatment with a CD73 antagonist or inhibitor.
Underlying medical conditions that, in the investigator or sponsor's opinion, will make the administration of study-specified therapy hazardous
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