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ENROLLING BY INVITATION
NCT06648785
PHASE2

Modified Capecitabine and Oxaliplatin (mCAPOX) for Patients With GI Malignancies

Sponsor: University of Vermont Medical Center

View on ClinicalTrials.gov

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

DRUG

oxaliplatin

85 mg/m2 oxaliplatin

DRUG

Fluoropyrimidine

oral fluoropyrimidine 1000mg/m2

Locations (2)

University of Vermont Medical Center

Burlington, Vermont, United States

University of Vermont

Burlington, Vermont, United States