Patient Guide: Safety of Trifluridine/Tipiracil in Patients With Dihydropyrimidine Dehydrogenase Deficiency Diagnosed With Metastatic Colorectal or Gastroesophageal Cancer

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 20 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06245356
Status: 🟢 Enrolling Now
Condition: Metastatic Colorectal Cancer, Metastatic Gastroesophageal Adenocarcinoma, DPD Deficiency
Phase: PHASE2

Where You Can Participate

This study is available at 20 locations across the country.

Top locations include:
  • • Amiens,
  • • Angers,
  • • Avignon,
  • • And 17 more locations

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Safety of Trifluridine/Tipiracil in Patients With Dihydropyrimidine Dehydrogenase Deficiency Diagnosed With Metastatic Colorectal or Gastroesophageal Cancer - Join Clinical Trial NCTNCT06245356

How to Join This Clinical Trial - NCTNCT06245356

Learn how to participate in this PHASE2 trial studying an investigational therapy for Metastatic Colorectal Cancer, Metastatic Gastroesophageal Adenocarcinoma, DPD Deficiency. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Metastatic Colorectal Cancer, Metastatic Gastroesophageal Adenocarcinoma, DPD Deficiency. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Metastatic Colorectal Cancer, Metastatic Gastroesophageal Adenocarcinoma, DPD Deficiency
Treatment Being Tested
Investigational treatment
Study Phase
PHASE2 - Safety and effectiveness study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06245356 - ClinicalTrials.gov Identifier
Sponsored By
Study sponsor

What to Expect as a Participant

Participating in this clinical trial involves:

  • Initial screening to determine eligibility
  • Regular study visits and health assessments
  • Receiving the study treatment or placebo
  • Medical monitoring and follow-up care
  • Contributing to medical research that may help others
  • Potential access to new treatments before they're widely available

Clinical Trial Benefits and Compensation

Participants in this clinical research study may receive:

  • Close medical monitoring by healthcare professionals
  • Access to potential new treatments
  • Compensation for time and travel (varies by study)
  • No-cost study-related medical care
  • The opportunity to help advance medical knowledge

Where Is This Clinical Trial Located?

This study is enrolling participants at 20 locations. Find a study site near you:

Clinical Research Site

Amiens, 80054 - France

Status: NOT_YET_RECRUITING

Clinical Research Site

Angers, 49055 - France

Status: NOT_YET_RECRUITING

Clinical Research Site

Avignon, 84918 - France

Status: ACTIVE_NOT_RECRUITING

Clinical Research Site

Besançon, 25000 - France

Status: ACTIVE_NOT_RECRUITING

Clinical Research Site

Cholet, 49300 - France

Status: ACTIVE_NOT_RECRUITING

Clinical Research Site

Dijon, 21079 - France

Status: WITHDRAWN

Clinical Research Site

Lyon, 69008 - France

Status: ACTIVE_NOT_RECRUITING

Clinical Research Site

Montpellier, 34298 - France

Status: ACTIVE_NOT_RECRUITING

Clinical Research Site

Paris, 75010 - France

Status: ACTIVE_NOT_RECRUITING

Clinical Research Site

Paris, 75012 - France

Status: RECRUITING

And 10 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE2 clinical trial for Metastatic Colorectal Cancer, Metastatic Gastroesophageal Adenocarcinoma, DPD Deficiency:

  1. Review the eligibility criteria with your healthcare provider
  2. Contact the study team for a pre-screening interview
  3. Schedule an in-person screening visit if eligible
  4. Review and sign the informed consent form
  5. Begin participation in the clinical trial

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