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Modified Capecitabine and Oxaliplatin (mCAPOX) for Patients With GI Malignancies
Sponsor: University of Vermont Medical Center
Summary
This study is a single arm, non-randomized feasibility study with tolerability and toxicity evaluation as primary endpoints which seeks to determine if a modified administration schedule of capecitabine with oxaliplatin will result in less toxicity than standard FOLFOX or CAPOX regimens.
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
20
Start Date
2024-10-21
Completion Date
2026-11
Last Updated
2026-02-05
Healthy Volunteers
No
Conditions
Interventions
oxaliplatin
85 mg/m2 oxaliplatin
Fluoropyrimidine
oral fluoropyrimidine 1000mg/m2
Locations (2)
University of Vermont Medical Center
Burlington, Vermont, United States
University of Vermont
Burlington, Vermont, United States