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Clinical Trial Summary

Catheter directed retrograde venous infusion of gemcitabine/lipiodol into pancreatic tumors.


Clinical Trial Description

Overall, subjects with resectable, borderline-resectable and/or locally-advanced pancreatic cancer are eligible to be entered into the study. Each enrolled study subject will receive a single neoadjuvant pancreatic retrograde venous infusion (PRVI) administration of the gemcitabine/Lipiodol® emulsion.

Complete enrollment in 12 months from date of enrollment of first study subject. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03865563
Study type Interventional
Source Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
Contact
Status Withdrawn
Phase Phase 1
Start date July 2019
Completion date December 2021

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