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NCT05266300

Implementation and Quality Assurance of DPYD-genotyping in Patients Treated With Fluoropyrimidines.

Completed Last updated 1 November 2022
What this trial tests

trial testing DPYD genotype in Adverse Drug Event in 722 participants. Completed in 1 October 2022.

Timeline
1 September 2020
Primary endpoint
1 June 2022
1 October 2022

Quick facts

Lead sponsorUniversity of Southern Denmark
StatusCompleted
Study typeOBSERVATIONAL
Enrollment722
Start date1 September 2020
Primary completion1 June 2022
Estimated completion1 October 2022
Sites1 location across Denmark

Drugs / interventions tested

Conditions studied

Sponsor

University of Southern Denmark

Who can join

18 and older, any sex, with Adverse Drug Event or Colon Cancer. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to examine the benefits of a clinical implementation of a DPYD-genotype test to patients starting treatment with fluoropyrimidines (Fluorouracil (5-FU), capecitabine, tegafur).

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Implementation and clinical benefit of DPYD genotyping in a Danish cancer population.
    Paulsen NH, Pfeiffer P, Ewertz M, Fruekilde PBN, et al · · 2023 · cited 10× · PMID 36791638 · DOI 10.1016/j.esmoop.2023.100782

Verify or expand the search:

Other recruiting trials for Adverse Drug Event

Currently open trials in the same condition.

Other University of Southern Denmark trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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