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Clinical Trial Summary

Using gemcitabine and nab-paclitaxel, the investigators hope to establish the differential ability of local and cytologically positive disease to respond to this regimen, and in particular, the frequency of cytologic conversion from positive to negative in such patients. The investigators also can begin to assess the value of maximum local therapy, including surgery, in patients who cytologically convert from positive to negative.


Clinical Trial Description

This research study is a Phase Ib clinical trial. It will assess the frequency of cytological conversion in patients with pancreatic adenocarcinoma and positive peritoneal cytology as a sole metastatic site following gemcitabine nab-paclitaxel. Subjects must have a newly diagnosed stage 4 untreated metastatic pancreatic ductal cancer with positive peritoneal cytology as a sole metastatic site and meet all inclusion/exclusion criteria. Treatment consists of 4 week treatment cycles. Nab-paclitaxel and gemcitabine will be administered on days 1,8, and 15. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03703089
Study type Interventional
Source Benaroya Research Institute
Contact Vincent J Picozzi, MD
Phone 206-223-6193
Email Vincent.Picozzi@virginiamason.org
Status Recruiting
Phase Phase 1
Start date May 1, 2018
Completion date May 1, 2023

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