Last reviewed · How we verify

NCT04894123

Cardiovascular Events From Trifluridine/Tipiracil +/- Oxaliplatin in Colorectal/Oesogastric Adenocarcinoma Patients

Terminated Phase 2 Last updated 18 September 2023
What this trial tests

Phase 2 trial testing Trifluridine/Tipiracil in Colorectal Adenocarcinoma in 1 participant. Terminated before completion.

Timeline
7 February 2022
Primary endpoint
13 February 2023
13 February 2023

Quick facts

Lead sponsorGERCOR - Multidisciplinary Oncology Cooperative Group
PhasePhase 2
StatusTerminated
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment1
Start date7 February 2022
Primary completion13 February 2023
Estimated completion13 February 2023
Sites11 locations across France

Drugs / interventions tested

Conditions studied

Sponsor

GERCOR - Multidisciplinary Oncology Cooperative Group

Who can join

18 and older, any sex, with Colorectal Adenocarcinoma or Oesogastric. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to assess the incidence of cardiovascular events in patients with esophageal/stomach or colorectal cancer treated by trifluridine/tipiracil +/- oxaliplatin after an episode of cardiac angina-related thoracic pain due to fluoropyrimidines in the adjuvant or metastatic setting .

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other trials of Trifluridine/Tipiracil

Trials testing the same drug.

Other recruiting trials for Colorectal Adenocarcinoma

Currently open trials in the same condition.

Other GERCOR - Multidisciplinary Oncology Cooperative Group trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04894123.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing