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This protocol will involve collection of blood samples from patients with a diagnosis of pancreatic adenocarcinoma for evaluation of circulating biomarkers.
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. Subjects who have any clinically significant psychiatric, social, or medical condition that, in the opinion of the investigator, could increase the patient's risk, interfere with protocol adherence, or affect the patient's ability to give informed consent are ineligible to participate in the study.
30 participants in 1 patient group
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Mark O'Hara, MD; Liudmila Mazaleuskaya, PhD
Data sourced from clinicaltrials.gov
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