Overview

DPYD Pharmacogenomics and Fluoropyrimidine (FP) Dose-Adjustment

Status:
NOT_YET_RECRUITING
Trial end date:
2029-07-07
Target enrollment:
Participant gender:
Summary
To prospectively evaluate the efficacy and safety of DPYD-guided dosing strategies in a real-world clinical setting, specifically by comparing the incidence of severe (Grade 3 and 4) fluoropyrimidine-related toxicities of heterozygous DPYD variant patients assigned to DPYD-guided reduced dosing versus patients with standard dosing in the control arm.
Phase:
PHASE4
Details
Lead Sponsor:
Rutgers, The State University of New Jersey
Treatments:
Capecitabine
Fluorouracil