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Clinical Trial Summary

Feasibility of neoadjuvant therapy in resectable biliary adenocarcinoma.


Clinical Trial Description

This trial will evaluate whether a neoadjuvant paradigm is feasible in resectable biliary adenocarcinoma. All components of therapy are currently used standards of care, however they have not been used in the neoadjuvant setting for the management of resectable biliary cancers. The study will use Gemcitabine/cisplatin, followed by chemoradiation. This is a feasibility trial with an accrual goal of 12 patients using the primary endpoint of completion of neoadjuvant therapy and surgery as an assessment of feasibility. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04480190
Study type Interventional
Source University of Cincinnati
Contact
Status Withdrawn
Phase Phase 1
Start date February 4, 2021
Completion date April 4, 2022

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